镭雕助剂LaserAT-8632浅标深添加剂说明书-en
美国火花科技产品说明书

WARNINGRISK OF IMPROPER FLAME DETECTION•Install only in areas in accordance with the environmental and hazardous area ratings.•Carefully review mounting area and position in accordance with the Performance Appendix and the User Manual to ensure optimal flame detection regarding the angle of device and unobstructed view.•Avoid potential sources of direct or indirect radiation in the flame detector field of view.•Do not touch the sensors on the front of the electronics module.•Avoid direct sunlight into the flame detector window –use provided sunshade,aim flame detectors down at 40degrees or more when possible,and use multiple detectors to cover hazardous areas from different directions.•Avoid close proximity to rapid modulation/chopping of sunlight (creating moving dark shadows)as optical sensor performance can be reduced,e.g.close trees in the wind,rotating blades.•Use shielded cable for all wirings and ground the shield at one end as detailed in the Wiring section.•Keep all devices and wire runs away from mercury vapor lights,variable speed drives,radio repeaters and other sources of electromagnetic interference.•Follow local cabling and glanding rules.•Seal all unused conduit entries and install proper drains/traps by local codes.•Do not try to service parts inside the electronics module,there are no field serviceable parts,just modulereplacement.CAUTIONRISK OF PRODUCT DAMAGE•Do not install in an area where there are incidents of high mechanical damage.•Protect controllers and monitors from physical damage (forklifts,etc.).•Failure to follow all warnings cautions,and instructions may void the warranty.•To maintain IPX6integrity,seal conduit entries with thread sealantsuch as Loctite 565or approvedequivalent.WARNINGRISK OF EXPLOSION•Ensure power is off and no hazardous gases nor dusts are present before installing or opening the device.•Use only hazardous location approved plugs plugs M25or ¾’’NPT as marked on product.SPECIFIC CONDITIONS OFUSE:WARNINGELECTROSTATIC HAZARD,DO NOT RUB WITH DRY CLOTH•Contact the manufacturer for dimensional information on the flameproof joint specifications if repair is required.QUICKREFERENCE GUIDEfor Hazardous Location InstallationSeries Flame Detectors and associated Test LampsThe Honeywell®Analytics Flame Detectors and Test Lamps are hazardous area products.They are factory calibrated,and the robust sealed design with no moving parts allows for mounting in any orientation even in harsh environments.These products are available in either a 316Stainless Steel or Low Copper Aluminum.Nameplate TagRepresentative Markings are displayed in the figure below.Additional regional marks(such as South Korea and Russia)and installation specific marks(such as ABS)may also be present.See individual nameplates for specific approvals applicable to each product. Note:Some products require18in.of conduit.(See individual nameplate for specifics). Electrical Ratings•Test Lamps(battery powered):12VDC,600mA•FS10:12VDC;60mA•FS10-R-A:Max29VDC,120mA;Relay24VDC,1A•FS20X and FS24X Series:Max32VDC,150mA;Relay24VDC,1A •FS20XP and FS24XP:Consumption18-32VDC,500mA max;Relay 24VDC/AC,2A maximumInstalling the Flame DetectorAll products are provided with a flameproof and explosion-proof enclosure and have been approved for use in Class1and Zone1 environments as specified on the individual product nameplate tag. Note:NFPA72and other local codes have specific requirements for flame detectors installations and must be consulted as necessary.Must only be installed by appropriately trained and accredited personnel.1.Securely mount the detector using minimum1/4-20or M6sized fasteners.Note:We recommend angling all detectors down at least40degrees fromhorizontal.2.Loosen,but do not remove the set screw on the coverassembly.3.Loosen the3Philips screws and remove the electro-opticalDetector Module and place face up in a safe location.Note:Do not drop the Detector Module and do not touch the sensor array.4.Connect the cable gland or conduit to the detector enclosurevia the¾’’NPT or M25openings,as per national electricalcodes for the install location.Connect the appropriate wiresrated for minimum85ºC to the field connectors provided asper the wiring diagram on the cover of the electro-opticalDetector Module.Ensure the enclosure is properly grounded in accordance withall local codes.Use shielded cable for all communications connections andground one end of the shield following the product manual. 5.Configure following the product's User Manual andPerformance Appendix to this guide.Note:Refer to the fuel and sensitivity settings table to determine the correctconfiguration.6.Connect the field connectors back onto the electro-opticalDetector Module and secure the module into the enclosurewith the Philips screws.7.Install the cover and ensure the O-ring is compressed.Tighten the cap screw on the cover assembly.Make a roughField of View(FoV)adjustment by aiming the detector at thearea you want to cover.8.Tighten all bolts when product has been fully configured andtested accordance with the product manual.Note:Detector functionality and communication should be tested to confirmcorrect FoV and configuration in the final system.Generic NameplateViewWARNINGRISK OF EXPLOSIONDo not connect test lamps to external power sources.Test lamps are battery operated only.Do not open when explosive gases are present. Charging permitted in safe environment only.Contact UsAmericas SwitzerlandHoneywell Analytics Main Phone:+41216953000405Barclay Boulevard***************************** Lincolnshire,Illinois60069Tel:+18479558200Asia PacificToll free:+18005380363Honeywell Industrial Safety***********************434,Worldcup Buk-ro,Mapo-gu Europe,Middle East,and Africa Seoul03922Honeywell International Sarl South Korea Piece16Tel:+82(0)2690903001180Rolle**************************Manuals,software,and other information about thisproduct are available atCopyright©2022,1701M5000HL Rev E October11,2022。
六合一细腺脂肪去脂RF辐射激光LLLT脂肪激光器说明书

6-1 Cellulite Removal Tripolar RF Diode Laser LLLT Lipo Laser Cavitation MachineUse ManualInstrument Function and Treatment Principles Product IntrodutionWave fat systemWith collective strong sound wave head, strong sound wave of 40000HZ may be emitted to vibrate fat cells at top speed and produce numerous vacuum air pockets inside and outside the fat cells, robustly impact fat cells to generate introverted blast and disintegrate triglyceride into glycerol and free fatty acids. Then RF waves at frequency of 1M HZ is used for exhausting the integrated glycerol and free fatty acids through hepatoenteral circulation. Finally, vacuum RF and energy electrode are used for positioning and tightening fat. In physics, it is known as "cavitations". Microspore introverted blast inside and outside cell may lead to enhanced molecular motion and a higher energy level and this will finally cause fat cell rupture and thereby achieve the effects of body building and losing weight.Lipo Laser systemit involves the application of a highly sensitive laser to dissolve the fat deposits situated in the upper layers of the human skin. The energy emanating from the laser breaks up the fat cells to produce an oily material. This substance is either naturally eliminated through normally bodily processes or can be removed via a small incision made by the practising surgeon. This leads to a permanent loss of fat as long as a healthy diet is maintained after treatment. It penetrate into skin surface and stimulates the fat cell membranes, changing their permeability, the fat cells reduce their overall size and intracellular fat is released then the fatty trigly cerides flow out of the disrupted cell membranes and into the interstitial space, where they gradually pass through the body's natural metabolic functions with no harmful physiological effects, this process is resulting in inch loss of patients.The subtlety of the treatment carries various advantages over the problems often associated with. Damaged blood vessels and allied physical risks are significantly reduced, and recovery time is condensed. It is also acknowledged that the laser itself is important in encouraging collagen production, thus strengthening the skin.Instrument Function and Treatment Principles 1. 40Khz Ultrasonic handle1. Strong sound wave explosion fat headWith collective strong sound wave head, strong sound wave of 40000HZ may be emitted to human body for impacting fat cells fiercely and Causing friction motion between fat cells. This may cause effective consumption of calories and moisture in fat cells and reduce the size of fat cells. What's more, sound wavevibration may cause fierce impact of fat cells to make them be exploded instantaneously, reduce the amount of fat cells and thereby achieve the effects of removing fat.Operation:1.Press to adjust the time.2. Select the strength by clicking to increase the strength or click to decrease it.3. Press to start the strong sound wave explosion fat head.4. Press to pause operation.Mode a. b. c. d means that:"A" is continuous working for 3 sec and discontinuous for 2 sec. "B" is continuous working for 4 sec and discontinuous for 3sec. "C" is continuous working for 1 sec and discontinuous for 1 sec.2."D" is continuous working for 0.5 sec and discontinuous for 0.5sec.2. Vacuum Bipolar RF handleFor body and face re-shaping and weight loss Vacuum + RF fat-explosion machine can promote tissue metabolism, repel the cellulite, which make fat granule in different depths and shocking make fusion energy, and the deepest receptor can get granule in3CM thick of skin, and rapid expansion and the rapid heating of the cell wall that exceed the elastic limits and arises cells broken, so that the combustion of fatty acids at the same time broken out of a pot, not only the burning consumption of fatty acids but also more directly emptying so rapidly reduce the size of granule.Operation:Body RF Probe (Vacuum) operation1. Press to adjust the time.2. Press to increase suction intensity or to decrease suction intensity3. Press to increase release intensity or to decrease release intensity.4. Press to increase the RF intensity or to decrease RFintensity.5. Press to start RF operation;6. Press to Pause operation.Beautifying: Use the probe to massage the specific part of skin circularly after applying the sliming cream for about 30 to 40 minutes. It could quicken the blood circulation in the part of skin treated and has the effect of decomposing fat, etc. Notes:1. Apply sliming cream or cooling gel to the part of skin to be treated before the treatment.2. Keep close contact between the probe and the skin.3. Adjust the intensity from low level to high level.4. Please do not irradiate eyeball directly with colored light.3.Tripolar RFStick to enhance rejuvenation: use of positive and negative micro-current activation energy release skin cells, so that paid synthesis of fibroblasts collagen, elastic skin revert to the original compact, the skin causing the eliminate wrinkles, prevent skin aging, restoring skin elasticity, facial improvement.Operation:1. Press to adjust the time.2. Select the strength by clicking to increase the strengthor click to decrease it.3. Press to start the strong sound wave explosion fat head.4. Press to pause operation.4. Body RF handleBeing integrated with the most advanced RF technology and radio frequency, the instrument may directly reach the deep-seated fat body and have the excellence oftargeted positioning RF. In thefast-active state, fat cell tissue may generate friction heat, increase local temperature and remove excess fat and toxin from the body through sweat gland,enter hepatic circulation and lymph and ultimately achieve the effect of dissolving fat. With controlled depth technology, inlaid diamond particles of different sizes may rub skin along its pattern, adjust suction strength by means of vacuum draw and rub with negative pressure strong force to directly explode thick fat. Thus, the effects are very the skin are also changed. By this time, natural electric resistance in the subcutaneous tissue moves and generates heat energy. As the papillary dermis collagen may immediately shrink when the temperature is within the range from 60 to 70 Celsius degree, after wrinkle treatment, client may immediately sense the skin tightening effects as it is being lifted and firmed. When collagen is produced continuously, thickness and density of the skin papillary dermis may be increased to remove wrinkles, eliminate scars, restore skin elasticity and gloss and make it be blonde and smooth. While collagen is increased, fresh skin is generated in the position of operation and wrinkles are removed by large amount of cells. In addition, when cortex without elasticity or that with thick horny layer in the area with wrinkles is separated, surrounding skin will also be renewed.Operation:1. Press to adjust the time.2. Select the strength by clicking to increase the strength or click to decrease it.3. Press to start the strong sound wave explosion fat head.4. Press to pause operation.5. Lipo Laser PaddlesIt involves the application of a highly sensitive laser to dissolve the fat deposits situated in the upper layers of the human skin. The energy emanating from the laser breaks up the fat cells to produce an oily material. This substance is either naturally eliminated through normally bodily processes or can be removed via a small incision made by the practising surgeon. This leads to a permanent loss of fat as long as a healthy diet is maintained after treatment. It penetrate into skin surface and stimulates the fat cell membranes,changing their permeability,the fat cells reduce their overall size and intracellular fat is released then the fatty trigly cerides flow out of the disrupted cell membranes and into the interstitial space,where they gradually pass through the body's natural metabolic functions with no harmful physiological effects,this process is resulting in inch loss of patients.Operation:1. Press to adjust the time.2. Select the strength by clicking to increase the strength or click to decrease it.3. Press to start the Lipo Laser.4. Press to pause operation.InstallationTechinical ParametersPower supply Input:110V/220V 60HZ/50HZ Power :130W40K cavitation head:Power supply output:150V Frequency:40KHz Power:25WVacuum+Bipolar RF head: Power supply output:66V Freqeuncy:450K Power:95W BIO head:Power supply output:24V Freqeuncy:1.5K Power:1WTripolar RF head:Power supply output:66V Freqeuncy:450K Power:35WFace RF head:Power supply output:66V Freqeuncy:450K Power:35WPackage Including:Multipolar RF head(Tripolar RF) X 1 40KHz Cavitation Head X 1 Vacuum Biploar Head x 1 Bipolar RF Head for face X 2 1xPower line(We offer 100-240V,AU/EU/UK/AU plug) 6xBig paddle with 8 diode laser//Each (Total 48 Diode laser) 2xSmall paddle with 3 diode laser//Each (Total 6 Diode laser) 1xMetal holder for diode paddlesBUTTOCKSILLUSTRATIN of OPERATIONFACETreated time: 30 minutes1. Massage the mandible center in circles to produce deep heat.2. Massage lower jaw in lines.3. Massage the triangle zone of both sides of the face in circles.4. Massage from jaw to angulus oris to ear in linesTHIGHTreated time: 30 minutes1. From down to upper, pushing to the groin to dredge the lymph.2. From down to upper, circling push by anticlockwise can help decomposing fatness.3. Also can push by come-and-go to decompose fatness.4. Pull from the knee and muscle texture to upper, can improve the curve. Treated time: 20 to 30 minutes1. Along the lymph direction, pulling to the waist.2. From upper to down, by anticlockwise gesture, pull come-and-go.3. Along the muscle of arm, pull up to lift and tight the muscle.BACKTreated time: 20 to 30 minutes1. First by come-and-go, pushing the bladder nerve 2 to 3 times.2. Circling by anticlockwise to stimulate the underarm lymph node.3. On the back, by anticlockwise circling, can help to decompose the fatness.ing lymph drainage gesture, pull the toxin to the lymph node, can helpimproving the back curve.ARMTreated time: 30 minutesBACK SIDE1.From the inner elbow to the armpit, doing lymph drainage.2. Circling to stimulate the lymph node.3. By anticlockwise or come-and-go pushing, decomposing the fatnes.4. From the elbow to the oxter, doing tightening gesture.Facade1. From the elbow to the oxter, doing tightening gesture.AbdomenTreated time: 20 to 30 minutes1.From small to large, by clockwise direction, circling around the navel, can helpperistalsis of the large intestine.2. From small to large, by anticlockwise direction, circling.3. From the belly and muscle texture, pull to the groin.4. Through lymph drainage gesture, taking the toxin to the place of groin.Attention:1. Pregnant women or women during in menses.2. Epileptic.3. Patients with malignancy.4. Patient whose wound after operation has not healed up.5. Acute inflammation or epidemical patients.6. Whom with heart diseases or with heart pacemaker.7. Who with kidney (gall-stone) disease.8. Who was embedded metal object or silica gel.9. Who in menses, birth control period, emiction incontinence period, or accepting the belly operation.10. Whose body always takes much inner hot.11. Who has the genetic hypersensitivity.Notice:1. Be sure to use the special ultrasonic gel.2. Avoid knocking the us head.3. For avoiding burning the head, during operation, please prepare enough ultrasonic gel.4. Don’t stay in one place, avoid treating on the bone.5. Don’t use disinfectant product to disinfect the us head. We suggest the wet cotton or dry towel enough.6. Check the machine power cord if it is connected well.7. If the machine will not use for a long time, please switch off it, and power off.8. Please take off all metal decoration from the operator and patient’s body.9. If continuous using 1 hour, please pause the machine about 10 minutes, then using again.10. During the operation, be sure not to accept other treatment.。
Intercrete 4850 (Formerly Cemprotec EF Primer) NXA

化学品安全技术说明书应急咨询电话(带值班时间)::Intercrete 4850 (Formerly Cemprotec EF Primer)化学品的推荐用途和限制用途Intercrete 4850 (Formerly Cemprotec EF Primer)GHS化学品标识:产品代码:NXA450+44 (0)191 469 6111 (24H)制造商Flexcrete Technologies Ltd.Tomlinson Road LeylandLancashire, United Kingdom PR25 2DY Tel: +44(0)1772 450950本安全技术说明书责任人的e -mail地址:安全技术说明书根据 GB/ T 16483-2008 和 GB/ T 17519-2013皮肤致敏物 - 类别 1危险性类别:信号词:警告危险性说明:可能造成皮肤过敏反应。
象形图:防范说明预防措施:戴防护手套。
避免吸入蒸气。
受沾染的工作服不得带出工作场地。
事故响应:如皮肤沾染: 用大量肥皂和水清洗。
脱掉所有沾染的衣服,清洗后方可重新使用。
如发生皮肤刺激或皮疹: 求医/就诊。
安全储存:不适用。
废弃处置:处置内装物/容器按照地方/区域/国家/国际规章。
GHS标签要素补充标签要素通风不充足时应戴合适的呼吸器。
:没有出现就供应商当前所知可应用的浓度,被分类为对健康或环境有害及因此需要在本节报告的添加剂。
职业暴露限制, 如果有的话, 列在第 8 节中。
用水冲洗口腔。
如有假牙请摘掉。
将患者转移到空气新鲜处,休息,保持利于呼吸的体位。
如物质已被吞下且患者保持清醒,可饮少量水。
如患者感到恶心就应停止,因为呕吐会有危险。
禁止催吐,除非有专业医疗人士指导。
如发生呕吐, 应保持头部朝下以避免呕吐物进入肺部。
如有害的健康影响持续存在或加重,应寻求医疗救治。
切勿给失去意识者任何口服物。
如失去知觉,应置于康复位置并立即寻求医疗救治。
聚氨酯用添加剂 CS 7439 126 C-C 安全技术说明书

安全技术说明书页: 1/11 巴斯夫安全技术说明书按照GB/T 16483编制日期 / 本次修订: 21.12.2022版本: 10.0日期/上次修订: 14.03.2016上次版本: 9.0日期 / 首次编制: 12.03.2008产品: 聚氨酯用添加剂 CS 7439/126 C-CProduct: ELASTOPAN CS 7439/126 C-C(30395604/SDS_GEN_CN/ZH)印刷日期 25.10.20231. 化学品及企业标识聚氨酯用添加剂 CS 7439/126 C-CELASTOPAN CS 7439/126 C-C推荐用途: 聚氨酯组分公司:巴斯夫(中国)有限公司中国上海浦东江心沙路300号邮政编码 200137电话: +86 21 20391000传真号: +86 21 20394800E-mail地址: **********************紧急联络信息:巴斯夫紧急热线中心(中国)+86 21 5861-1199巴斯夫紧急热线中心(国际):电话: +49 180 2273-112Company:BASF (China) Co., Ltd.300 Jiang Xin Sha RoadPu Dong Shanghai 200137, CHINA Telephone: +86 21 20391000Telefax number: +86 21 20394800E-mail address: ********************** Emergency information:Emergency Call Center (China):+86 21 5861-1199International emergency number: Telephone: +49 180 2273-1122. 危险性概述纯物质和混合物的分类:急性毒性: 分类4 (口服)严重损伤/刺激眼睛: 分类1巴斯夫安全技术说明书日期 / 本次修订: 21.12.2022版本: 10.0产品: 聚氨酯用添加剂 CS 7439/126 C-CProduct: ELASTOPAN CS 7439/126 C-C(30395604/SDS_GEN_CN/ZH)印刷日期 25.10.2023 特异性靶器官毒性-反复接触: 分类2 (口服)标签要素和警示性说明:警示词:危险危险性说明:H302吞咽有害。
镭神激光传感器产品手册说明书

目录镭神LS10A系列激光传感器 (3)镭神LS10B系列高速高精度激光传感器 (5)镭神LS11A系列激光位移传感器 (7)镭神LS11B系列高速激光位移传感器 (9)镭神LS50系列TOF激光测距传感器 (11)镭神相位法激光传感器 (12)镭神三维激光扫描仪 (13)镭神LS10A系列激光传感器LS10A基本概况LS10A系列激光传感器是深圳市镭神智能系统有限公司研发的近距离高精度的非旋转扫描测距产品。
该传感器运用激光三角法测量物体三维尺寸,可完成物体检查、定位、测量等多种工作任务,帮助客户提高生产力,实现生产控制和质量控制。
LS10A系列激光传感器的扫描频率30Hz,采用USB接口输出数据,根据测量尺寸的不同,可划分为不同的产品型号,具体参数如下表所示。
产品参数LS10A-050 LS10A-095 LS10A-245 LS10A-350 量程起点50mm 70mm 170mm 200mm量程中点55mm 95mm 245mm 350mm量程终点60mm 120mm 320mm 500mm 高度方向测量范围10mm 50mm 150mm 300mm±0.17%FSO ±0.10%FSO ±0.13%FSO ±0.40%FSO5μm 20μm 50μm 1200μm 量程起点10mm 14mm 34mm 40mm量程中点11mm 19mm 49mm 70mm量程终点12mm 24mm 64mm 100mm360测量点/扫描线标准655nm 655nm 655nm 655nm可选405nm 405nm 405nm 405nm2M5mW 8 mW 10 mW 15 mW30° 30° 30° 30°10000lx 10000lx 5000lx 5000lx30Hz 30Hz 30Hz 30HzUSBUSB不锈钢5VDC,±10%IP65阳极氧化铝/不锈钢PMMA/安全玻璃15g2g/20~500Hz0℃~40℃-20℃~+70℃产品应用物体检查形状测量镭神LS10B系列高速高精度激光传感器LS10B基本概况LS10B系列激光传感器是深圳市镭神智能系统有限公司研发的高速高精度的扫描测距产品。
BAOSR6x86.03 OSR General Chemistry 产品说明书

BAOSR6x86.03 OSR General Chemistry 2012-01 IRONOSR6186 4 x 15 mL R14 x 15 mL R2OSR6286 4 x 30 mL R1 4 x 30 mL R2Intended UseSystem reagent for the quantitative determination of Iron in human serum on Beckman Coulter AU analyzers.Summary Iron (non-heme) measurements are used in the diagnosis and treatment of diseases such as iron deficiency anemia, hemochromatosis (a disease associated with widespread deposit in the tissues of two iron-containing pigments, hemosiderin and hemofuscin, and characterized by pigmentation of the skin), and chronic renal disease. Transferrin is the major iron carrying protein in the serum.MethodologyIn 1954, Schade et al.1introduced a method for the direct determination of serum iron. The iron level was determined by incubating the serum in a phosphate buffer with ascorbic acid and terpyridine. Goodwin,2 in 1966, proposed a direct method for serum iron using an acetate buffer andbathophenanthroline. These modifications eliminated random iron contamination from phosphate buffers and enhanced color development by using a more sensitive iron chromogen.This Beckman Coulter method utilizes a variation of these methods using TPTZ [2,4,6-Tri-(2-pyridyl)-5-triazine] as the chromogen.3In an acidicmedium, transferrin-bound iron dissociates into free ferric ions and apo-transferrin. Hydrochloric acid and sodium ascorbate reduce the ferric ions to the ferrous state. The ferrous ions then react with TPTZ to form a blue colored complex which can be measured bichromatically at 600/800 nm. The increase in absorbance is directly proportional to the amount of transferrin bound iron present.Buffer Transferrin 2 (Fe 3+) 2 (Fe 3+) + Apo-transferrin2 Fe 3+ + Ascorbic Acid + 2 H 2O 2 Fe 2+ + Dehydroascorbic Acid + 2 H 30+Fe 2+ + TPTZ Iron-complex (blue colored complex)System Information For AU400/400e /480, AU600/640/640e/680 and AU2700/5400/AU5800 Beckman Coulter Analy z ers .ReagentsFinal concentration of reactive ingredients:Glycine buffer (pH 1.7) 215mmol/L L-Ascorbic Acid 4.7mmol/L 2,4,6-Tri-(2-pyridyl)-5-triazine 0.5mmol/L Also contains preservativesPrecautions1. For in vitro diagnostic use.2. WARNING! CORROSIVE! Do not pipet by mouth. Avoid contact with eyes, skin or clothing. In case of contact, immediately flush affected areawith plenty of water for 15 minutes. Obtain medical attention immediately for eye contact or ingestion.Preparation of ReagentsThe Iron Reagents are ready for use. No preparation is required.Storage and StabilityThe reagents are stable, if unopened, up to the stated expiration date when stored at 2 - 8°C. Opened reagents are stable for 60 days when stored in the refrigerated compartment of the analyzer.The color of R1 turns to brown during the course of the shelf life. This does not restrict any function of this reagent as long as reagent OD results on the analyzer are within specified limits.Indications of DeteriorationVisible signs of microbial growth, turbidity or precipitation or any change in the color of the reagent may indicate degradation and warrantdiscontinuance of use.Specimen Collection and PreparationSerum or heparinized plasma samples, free from hemolysis, are the recommended specimens. Remove serum from the red cells to minimize hemolysis as hemolyzed samples may produce erroneous results. Plasma specimens collected with EDTA, oxalate, or citrate are unsatisfactory, since they bind iron, preventing its reaction with the chromogen. Samples should be taken in the morning from patients in a fasting state, since iron values decrease by 30% during the course of the day 4 and there can be significant interference from lipemia.Sample Storage and Stability Serum iron is stable for 7 days when stored at 2 - 8°C or 4 days at room temperature (15 - 25°C) after the serum is separated from red cells.5IronInterfering SubstancesResults of studies6 show that the following substances interfere with this iron procedure when tested at 150 µg/dL Iron.The criteria for no significant interference is recovery within 10% of the initial value.Bilirubin: No significant interference up to 40 mg/dL BilirubinCopper: No significant interference up to 1 mg/dL CopperGlobulin: No significant interference up to 5 g/dL Human Gamma GlobulinLipemia: No significant interference up to 400 mg/dL Intralipid*Hemolysis*** Intralipid, manufactured by KabiVitrium Inc., is a 20% IV fat emulsion used to emulate extremely turbid samples.** Hemolyzed samples should not be tested. Hemolyzed samples may react with the reagent producing results with a negative bias.In very rare cases gammopathy, especially monoclonal IgM (Waldenström’s macroglobulinemia), may cause unreliable results10.The information presented is based on results from Beckman Coulter studies and is current at the date of publication. Beckman Coulter Inc., makes no representation about the completeness or accuracy of results generated by future studies. For further information on interfering substances, refer to Young for a compilation of reported interferences with this test.7ProcedureA complete list of test parameters and operational procedure can be found in the User’s Guide appropriate to the analyzer.Materials ProvidedIron ReagentMaterials Required But Not ProvidedChemistry Calibrator (Cat # DR0070)Stability of Final Reaction MixtureThe Beckman Coulter AU analyzer automatically computes every determination at the same time interval.CalibrationThe frequency of calibration is 30 days. Calibration of this iron procedure is accomplished by use of the Chemistry Calibrator (Cat # DR0070), which is traceable to the National Institutes of Standards and Technology (NIST) Standard Reference Material (SRM) 1598 and 937.Recalibration of this test is required when any of these conditions exist:1. A reagent lot number has changed or there is an observed shift in control values.2. A fresh bottle of reagent is used for testing.3. Major preventative maintenance was performed on the analyzer or a critical part was replaced.Quality ControlDuring operation of the Beckman Coulter AU analyzer at least two levels of an appropriate quality control material should be tested a minimum of once a day. In addition, controls should be performed after calibration, with each new lot of reagent, and after specific maintenance or troubleshooting steps described in the appropriate User’s Guide. Quality control testing should be performed in accordance with regulatory requirements and each laboratory’s standard procedure.ResultsAutomatically printed out for each sample in µg/dL at 37°C. For SI units (µmol/L) multiply result by 0.179.Dynamic RangeThe Iron procedure is linear from 10 to 1000 µg/dL. Samples exceeding the upper limit of linearity should be diluted and repeated. The sample may be diluted, repeated and multiplied by the dilution factor automatically by utilizing the AUTO REPEAT RUN.Expected ValuesAdult:850 - 212 µg/dLExpected values may vary with age, sex, diet and geographical location. Each laboratory should determine its own expected values as dictated by good laboratory practice.Specific Performance CharacteristicsThe following data was obtained using the Iron Reagent on Beckman Coulter AU analyzers according to established procedures. Results obtained in individual laboratories may differ.Precision11Estimates of precision, based on CLSI recommendations9, are consistent with typical performance. The within run precision is less than 3% CV and total precision is less than 5% CV.Assays of control sera were performed and the data reduced following CLSI guidelines above:N = 60 Within run TotalMean, µg/dL SD CV% SD CV%53.6 0.54 1.02 1.12 2.09158 1.05 0.66 2.8 1.77589 3.81 0.65 7.23 1.23OSR General Chemistry BAOSR6x86.032012-01IronBAOSR6x86.03 OSR General Chemistry2012-01 Method Comparison 11 Patient samples were used to compare this Iron Reagent. The table below demonstrates representative performance on AU analyzers. Y Method AU640X Method OSR6123/6223Slope 1.040Intercept 2.23Correlation Coeff. (r) 0.995No. of Samples (n) 96Range (µg/dL) 11.60-253SensitivityTypical change in absorbance for 1 µg/dL of Iron is 0.2 mAbsorbance.References1. Schade, A., Ogama, J., Reinhart, R., and Miller, J., Proc. Soc. Exp. Biol. Med., 87: 442, 1954.2. Goodwin, J., Murphy, B., and Guillemette, M., Clin. Chem., 12: 47, 1966.3. Diehl, H., and Smith, G.F., “The Iron Reagents, Bathophenanthroline, 2,4,6-Tripyridyl-s-triazine, Phenyl-2-pyridylocine”, GF Smith Chem Co, 1960.4. Tietz, N.W. Textbook of Clinical Chemistry, WB. Saunders, 1580, 1986.5. Henry, R.J. et al. Clinical Chemistry: Principles and Technics, Harper and Row, 1974.6. CLSI/NCCLS, Interference Testing in Clinical Chemistry EP7-P, 1986.7. Young, D.S., Effects of Drugs on Clinical Laboratory Tests, 5th Edition, AACC Press, 2000.8. Beckman Coulter Inc. data on samples collected from 200 blood donors in North Texas.9. CLSI/NCCLS Evaluation Protocol, EP5-T2, 1992.10. Bakker, A.J., Clin. Chem. 37:690,1991.11. Data is on file for specific AU analyzers.Manufactured by: Beckman Coulter, Inc., 250 S. Kraemer Blvd. Brea, CA 92821, USA。
Roxtec产品说明书
Lubricate the inside of the framethoroughly, especially into thecorners.If the frame is provided with a net,cut or bend the net with a sharptool, or your fingers, to enablecables/pipes to pass through attheir position in the frame.Pull the cables through. Please seenote on reverse page.by more than one layer.Remove any dirt from the sleeve/hole.Installation instructionsRoxtec R frame InstallationR 70 70-71 75 40 x 40R 75 75-76 75 40 x 40R 100 100-102 80 60 x 60R 125 125-127 75 80 x 80R 127 127-129 75 80 x 80R 150 150-152 75 90 x 90R 200200-20275120 x 120Roxtec ® and Multidiameter ® are registered trademarks of Roxtec in Sweden and/or other countries.R 70-R 127 6-7R 150-R 2009-11Torque settingssealed. Please see recommended torque in the table.11plan (transit plan).12DISCLAIMER”The Roxtec cable entry sealing system (”the Roxtec system”) is a modular-based system of sealing products consisting of different components. Each and every one of the components is necessary for the best performance of the Roxtec system. The Roxtec system has been certified to resist a number of different hazards. Any such certification, and the ability of the Roxtec system to resist such hazards, is dependent on all components that are installed as a part of the Roxtec system. Thus, the certification is not valid and does not apply unless all components installed as part of the Roxtec system are manufactured by or under license from Roxtec (“authorized manufacturer”). Roxtec gives no performance guarantee with respect to the Roxtec system, unless (I) all compo-nents installed as part of the Roxtec system are manufactured by an authorized manufacturer and (II) the purchaser is in compliance with (a), and (b), below.(a) During storage, the Roxtec system or part thereof, shall be kept indoors in its original packaging at room temperature.(b) Installation shall be carried out in accordance with Roxtec installation in-structions in effect from time to time.The product information provided by Roxtec does not release the purchaser of theRoxtec system, or part thereof, from the obligation to independently determine the suitability of the products for the intended process, installation and/or use.Roxtec gives no guarantee for the Roxtec system or any part thereof and as-sumes no liability for any loss or damage whatsoever, whether direct, indirect, consequential, loss of profit or otherwise, occurred or caused by the Roxtec systems or installations containing components not manufactured by an authorized manufacturer and/or occurred or caused by the use of the Roxtec system in a manner or for an application other than for which the Roxtec system was designed or intended.Roxtec expressly excludes any implied warranties of merchantability and fitness for a particular purpose and all other express or implied representations and warranties provided by statute or common law. User determines suitability of the Roxtec system for intended use and assumes all risk and liability in con-nection therewith. In no event shall Roxtec be liable for indirect, consequential, punitive, special, exemplary or incidental damages or losses.”DisassemblyReverse orderNoteFor optimum reliability, wait 24 hours or longer after installation before exposing the cables/pipes to strain or pressure. To be used with: RM modules.Cables/pipes shall be parallel to the sleevehole.Cable/pipe with a considerable weight needs to be supported to prevent damage or subsidence to the seal.Article number: ASS2005002501Document number: ASS2005002501 version CType: Rec. torque* (Nm)Aperture dimensionsType: Aperture Clearance Packing Ø (mm) depth (mm) space (mm)* The recommended torque depends on several things, e.g cable or pipe size, amount of used lubricant, sleeve size or material in the cable sheath, etc.。
镭雕培训手册
Violino™ DPSS全风冷半导体泵浦激光标记系统前言为加强对高速成长的亚洲市场的全方位支持,LASERVALL(镭射谷)集团2003年在中国深圳设立了“镭射谷科技(深圳)有限公司,为中国首家外商独资的工业激光应用系统高科技企业。
镭射谷科技(深圳)有限公司以LASERVALL先进的激光专有技术为核心,针对中国的工业特点和要求,对LASERVALL的系列产品进行进一步的技术开发、研制和生产。
镭射谷科技(深圳)有限公司的设立,极大地加强了中国境内用户的技术支持和服务。
镭射谷科技(深圳)有限公司的产品除在中国市场销售外,也批量销售到世界各地的市场。
LASERVALL公司拥有VIOLINOTM (微欧力诺™)品牌的红外光、绿光、紫光全频谱系列的光纤耦合全固态风冷半导体激光系统,公司产品技术领先、性能优越、应用广泛,在激光标记等工业应用领域享有世界声誉。
LASERVALL的产品已经全部通过国际权威的ISO9001的认证值得注意的是近年来发展起来的半导体激光器。
半导体激光器具有小型化、频率极高、与光纤良好耦合、易于调制等优良特性,因而具有广阔的应用前景。
要在不同产业中广泛应用激光制造技术,很大程度上要依赖于激光加工系统的性能与工艺。
欧、美、日及意大利一些国家在新光源、加工系统及工艺等方面的研究与开发就从未降温过。
随着激光工作物质的研究与开发、器件与单元技术的改进和创新,以高性能、宽波段、大功率为特征的激光取得了蓬勃的发展,如紫外光输出的KrF、ArF 准分子激光器、倍频激光器等。
尤其是高功率光纤激光的出现,使激光制造的移动式定位加工变得更加便利。
Violino™ DPSS全风冷半导体泵浦激光标记系统安装要求激光系统的现场安装要求:电源,接地,温度,湿度,电磁干扰,振动,水源,气源(1)、场地要求:镭射机应尽量选择安装在不小于10m2的独立封闭的操作室内。
地面水平、硬实、防震,门口粘贴激光防护标识。
如安装在流水线上,则需要根据现场情况,落实激光防护措施,包括粘贴激光防护标识。
金属加工--V-LASER-ON.PT说明书
¡Hola!Somosel nuevo socio de su produc ciónSomos especialistas en soldadura manual y robótica,plegado,corte por láser y pintura electrostática para la fabricación deCONJUNTOS METÁLICOSSOLDADOS COMPLEJOSLOTES Y SÉRIES DE PIEZAS PARA FABRICANTES DE EQUIPOS ORIGINALES Y FABRICANTES DE MAQUINARIA3plantas>3.850m2Oficina Técnica de Diseño e Ingeniería de ProducciónUbicación estratégica a10minutos del aeropuerto de Porto y del puerto de Leixões,el segundo más grande de Portugal.La excelencia es nuestra motivación¡Perseguimos la perfección en cada detalle!Estamos orgullosos de nuestro equipo de soldadoresaltamente calificados que combinan la excelenciade la fabricación portuguesa con la últimatecnología de soldadura robótica.Nuestros ingenieros y diseñadores le brindarántodo el soporte que necesita en cada etapa de producción paraSIMPLIFICAR SU TRABAJO.Por estas razones somos el proveedor elegido por los fabricantesque buscan el mejor servicio LLAVE EN MANO SIN PREOCUPACIONES Y CON UNPRECIO COMPETITIVO.LA CALIDAD DE NUESTRO TRABAJOSE VERIFICA REGULARMENTE BAJOEL ESTÁNDAR ISO ⁹⁰⁰¹:₂⁰¹₅.excelência'19Somos la extensión de su línea de producción¡PÍDENOS UN PRESUPUESTO!A su ladoen todaslas etapas del proyectoLA CLAVE DELÉXITO ESCONFIAR EN EL SOCIO ADECUADO¡HABLA CON UN EXPERTO!Nuestro departamento técnico responde a suspreguntas sobre materiales y tecnologías disponibles.¡SIMPLIFICA LA PRODUCCIÓN!Ofrecemos un servicio completo utilizando latecnología avanzada de TRUMPF®,HAAS®e FRONIUS®.SOLDADURA MANUAL Y ROBÓTICAPLEGADO DE CHAPACORTE DE CHAPA POR LÁSERPINTURA ELECTROSTÁTICAMONTAJE DE PRODUCTO¡CREA UN PRODUCTO PERFECTO!La calidad de nuestro trabajo se refleja en la satisfacción de sus clientes.La mejor tecnologíapara la eficienciaMÁQUINAS DE CORTE POR LÁSERTRUMPF®TruLaser5030(láser de CO2) TRUMPF®TruLaser3030fiber(láser de estado sólido)MÁQUINAS DE PLEGADO TRUMPF®TruBend5130RICO®PRCN I-Line2070TORNO CNCHAAS®ST10YFRESADORAHAAS®TM-2PROBOT DE SOLDADURA FANUC®ARC Mate100equipado con FRONIUS®TPS400iSISTEMAS DE SOLDADURA MANUAL 8MIG FRONIUS®VarioStar25002TIG+MIG FRONIUS®Synergic270 1TIG FRONIUS®MagicWave22001TIG FRONIUS®TransTig1700 1TIG KÜHTREIBER®KITin1700HF1ELECTREX®THI301KÖCO®KST108SERVICIO DE PINTURA ELECTROSTÁTICALimpieza>Secado>Pintura>PolimerizaciónSOFTWARE DE DISEÑOSOLIDWORKS®ProgeCAD®。
RayBio Mouse PAI-I IQLEISA Kit 使用手册说明书
RayBio® Mouse PAI-I IQLEISA KitCatalog #: IQM-PAIIUser ManualLast revised May 17, 2022Caution:Extraordinarily useful information enclosedISO 13485 Certified3607 Parkway Lane, Suite 100Norcross, GA 30092 Tel: 1-888-494-8555 (Toll Free) or 770-729-2992, Fax:770-206-2393Web: , Email: *******************RayBiotech, Inc.________________________________________RayBio® Mouse PAI-I IQLEISA Kit ProtocolTable of ContentsSection Page # I.Introduction3II.Reagents3III.Storage3IV.Additional Materials Required4V.Reagent Preparation4VI.Assay Procedure5VII.Assay Procedure Summary7VIII.Calculation of ResultsA. Typical DataB. Sensitivity and Recovery 8 9 9IX.Troubleshooting Guide10I. INTRODUCTIONThe RayBio®I mmuno Q uantitative E nzyme L inked I mumuno S orbent A ssay (IQELISA) is an innovative new assay that combines the specificity and ease of use of an ELISA with the sensitivity of real-time PCR. This results in an assay that is simultaneously familiar and cutting edge and enables the use of lower sample volumes while also providing more sensitivity. The RayBio® Mouse PAI-I IQLEISA Kit is a modified ELISA assay with high sensitivity qPCR readout for the quantitative measurement of Mouse PAI-I in serum, plasma, and cell culture supernatants. This assay employs an antibody specific for Mouse PAI-I coated on a 96-well PCR plate. Standards and samples are pipetted into the wells and PAI-I present in a sample is bound to the wells by the immobilized antibody. The wells are washed and a detection affinity molecule is added to the plates. After washing away unbound detection affinity molecule, primers and a PCR master mix are added to the wells and data is collected using qPCR. C t values obtained from the qPCR are then used to calculate the amount of antigen contained in each sample, where lower C t values indicate a higher concentration of antigen.II. REAGENTS1.PAI-I Microplate (Item A)**: 96 well PCR plate coated with anti-Mouse PAI-I.2.Wash Buffer I Concentrate (20x) (Item B): 25 ml of 20x concentrated solution.3.Standards (Item C): 2 vials of recombinant Mouse PAI-I.4.Assay Diluent A (Item D): 30 ml diluent buffer, 0.09% sodium azide as preservative. ForStandard/Sample (serum/plasma) diluent.5.Assay Diluent B (Item E): 15 ml of 5x concentrated buffer. For Standard/Sample (cellculture medium/urine) diluent.6.Detection Affinity Reagent for PAI-I (Item F): 2 vials of a 4x concentrated solution of anti-Mouse PAI-I affinity reagent.7.IQELISA Detection Reagent (Item G): 1.4mL of a 10x concentrated stock.8.Primer Solution (Item I): 1.7mL vial.9.PCR Master Mix (Item J): 1.2mL vial.10.PCR Preparation buffer (Item K): 1mL vial of 10x concentrated buffer.11.Final Wash Buffer (Item L): 10ml vial of 10x concentrated buffer.**The PCR plate used is a 0.2mL, non-skirted 96-well plate (ThermoFisher, cat. no.:AB0600). Please ensure compatibility with your PCR machine prior to purchase. For additional information contact technical support (**************************).III. STORAGEMay be stored for up to 6 months at 2°to 8°C from the date of shipment. Standard (recombinant protein) should be stored at -20°C or -80°C (recommended at -80°C) after reconstitution. Opened PCR plate or reagents may be stored for up to 1 month at 2° to 8°C. Note: the kit can be used within one year if the whole kit is stored at -20°C. Avoid repeatedfreeze-thaw cycles.IV. ADDITIONAL MATERIALS REQUIRED1.Real-time PCR instrument, Bio-Rad recommended2.Precision pipettes to deliver 2µl to 1 ml volumes.3.Adjustable 1-25 ml pipettes for reagent preparation.4.100 ml and 1 liter graduated cylinders.5.Absorbent paper.6.Distilled or deionized water.7.Log-log graph paper or computer and software for data analysis.8.Tubes to prepare standard or sample dilutions.9.Heating block or water bath capable of 80°CV. REAGENT PREPARATION1.Bring wash buffer, samples, assay diluents, and PCR plate to room temperature (18 - 25°C) before use. PCR master mix and Primer solution should be kept at 4°C at all times.2.Sample dilution: If your samples need to be diluted, 1x Assay Diluent B should be usedfor dilution of serum/plasma samples. Assay Diluent A maybe used in place if significant matrix affects are seen.Suggested dilution for normal serum/plasma: 2 -20 fold*.*Please note that levels of the target protein may vary between different specimens.Optimal dilution factors for each sample must be determined by the investigator.3.Assay Diluent B should be diluted 5-fold with deionized water.4.Briefly spin the Detection Antibody vial before use. Add 25 µl of 1X Assay Diluent B intothe vial to prepare a detection antibody concentrate. Pipette up and down to mix gently (the concentrate can be stored at 4°C for 5 days). This concentrate should be diluted 80-fold with 1X Assay Diluent B and used in step 4 of the Assay Procedure.5.PCR preparation buffer should be transferred to a 15mL tube and diluted with 9mL ofdeionized or distilled water before use.6.Final Wash Buffer should be transferred to a 15mL tube and diluted with 9mL ofdeionized or distilled water for every 1mL of 10x concentrate used before use.7.Preparation of standard: Preparation of standard: Briefly spin a vial of Standards. Add400 µl 1X Assay Diluent B into Standards vial to prepare a 100 ng/ml standard solution.Dissolve the powder thoroughly by a gentle mix. Add 100 µl of the PAI-1 standard from the vial of Standards, into a tube with 400 µl 1X Assay Diluent B to prepare a 20,000pg/ml standard solution. Pipette 200 µl 1X Assay Diluent B into each tube. Use the 20,000 pg/ml standard solution to produce a dilution series (shown below). Mix each tube thoroughly before the next transfer. 1X Assay Diluent B serves as the zero standard (0 pg/ml).400 µl + 100 µl100 µl+ 200 µl100 µl+ 200 µl100 µl+ 200 µl100 µl+ 200 µl100 µl+ 200 µl100 µl+ 200 µl20000 pg/ml 6666.667pg/ml2222.222pg/ml740.741pg/ml246.914pg/ml82.305pg/ml27.435pg/mlpg/ml8.If the Wash Buffer Concentrate (20x) contains visible crystals, warm to roomtemperature and mix gently until dissolved. Dilute 20 ml of Wash Buffer Concentrate into deionized or distilled water to yield 400 ml of 1x Wash Buffer.9.Prepare the IQELISA detection reagent by calculating how much will be needed. Thismay be accomplished by multiplying the number of wells to be assayed by the volume you plan to use per well. Once the volume of IQELISA detection reagent is known,prepare the reagent by diluting it 1:10 with deionized water and mixing thoroughly.VI. ASSAY PROCEDURE1.Bring all reagents and samples to room temperature (18 - 25°C) before use. It isrecommended that all standards and samples be run in triplicate. Partial plate runs may be accomplished by cutting the PCR plate into the desired number of strips using a pair of sturdy scissors, wire cutters, or shears. The remainder may be saved and used for a later date. If this is done, the PCR Plate Film should also be cut to a suitable size.2.Add 10-25µl of each standard (see Reagent Preparation step 2) and sample intoappropriate wells. Volumes should be consistent between all wells, samples, andstandards. As little as 10µL can be used if sample volume is limited, however thisincreases the chance of technical error. Ensure there are no bubbles present at thebottom of the wells. Dislodge any bubbles with gentle tapping or with a pipette tip being careful not to contact the sides or bottom of the well. Cover well and incubate for 2.5hours at room temperature or overnight at 4°C with gentle shaking.3.Discard the solution and wash 4 times with 1x Wash Solution. Wash by filling each wellwith Wash Buffer (100 µl) using a multi-channel Pipette or autowasher. Completeremoval of liquid at each step is essential to good performance. After the last wash, remove any remaining Wash Buffer by aspirating or decanting. Invert the plate and blot it against clean paper towels.4.Add 25 µl of prepared Detection Antibody (Reagent Preparation step 4) to each well.Incubate for 1 hour at room temperature with gentle shaking.5.Discard the solution. Repeat the wash as in step 3.6.Add 25µL of prepared IQELISA detection reagent and incubate 1 hour with rocking(Reagent Preparation step 9)7.Discard the solution. Repeat the wash as in step 3.8.Add 100µL of Final wash buffer to each well and incubate for 5 minutes with rocking.Remove the solution from each well and repeat an additional 2x.9.Add 100µL of 1x PCR preparation buffer to each well and incubate with rocking for 5minutes before removing the buffer. Blot the plate after the buffer is removed to ensure complete removal of the buffer.10.Add 15µL of the Primer solution to each well of the plate. At this stage the plate can becovered and stored at -20°C for use the next day if needed.11.Add 10µL of PCR Master Mix to each well and pipette thoroughly to mix the well (atleast 3x up and down).12.Cover the plate with the supplied PCR Plate Film, taking care to insure the film iscompletely and even pressed onto the plate, creating an air tight seal around each well of the plate.13.Place the plate into a real-time PCR instrument using a FITC compatible wave length fordetection with the following settings for cycling1.3 minute activation at 95°C2.10 seconds 95°C denaturation3.25 seconds 62°C annealing/extension4.Repeat steps 2 and 3 29xVII. ASSAY PROCEDURE SUMMARY1.Prepare all reagents, samples and standards as instructed.2.Add 25µl standard or sample to each well.Incubate 2.5 hours at room temperature or overnight at 4°C.3.Add 25µl Detection Antibody to each well.Incubate 1 hour at room temperature.4.Add 25µL of IQELISA Detection Reagent to each well. Incubate 1 hour5.Add 15µl Primer solution and 10µL of PCR master mix to each well6.Run real-time PCRVIII. CALCULATION OF RESULTSThe primary data output of the IQELISA kit is C t values. These values represent the number of cycles required for a sample to pass a fluorescence threshold. As the DNA is amplified additional fluorescent signal is produced, with each cycle resulting in an approximate doubling of the DNA. Therefore, higher levels of DNA (directly related to the amount of antigen in the sample) result in lower C t values.Calculate the mean C t for each set of triplicate standards, controls and samples. Subtract the C t value of each sample from the control to obtain the difference between the control and sample (Delta C t). Plot the values of the standards on a graph using a log scale for concentration on the x axis. This graph is the quickest way to visualize results, although not the most accurate. If this method is used the concentration of unknown samples can be estimated using a logarithmic line of best fit.The line of best fit will have an equation y = mln(x)+b, where y is the Delta C t value and x is the concentration. It may be helpful to use 5 significant figures for m and b to minimize rounding errors. To calculate the concentration of unknown sample this can be entered into Excel in the following format=EXP((y-b)/m))Where y is the Delta C t obtained during the assay, and b and m are obtained from the line of best fitAlternatively, for a more accurate representation linear regression may be used. Both the Delta C t and Concentration can be transformed using a log base of 10, plotted on a graph as described above, along with a line of best fit (using a linear model). The equation of this line may be used to calculate the antigen concentration of unknown samples. This is the method used for the analysis spreadsheet for IQELISA available online.A. TYPICAL DATAThese data are for demonstration only. A standard curve must be run with each assay.B. SENSITIVITY and RECOVERYThe minimum quantifiable dose of PAI-I is typically 78.125 pg/ml, however levels as lower than 78.125 pg/ml may be detected outside of the quantification range.Serum spike tests show recovery is 75% with a range from 67% to 80%ntraplate CV is below 10% for all samples and Interplate CV is below 15%X. TROUBLESHOOTING GUIDEProblem Cause SolutionPoor standard curve Inaccurate pipettingImproper standard dilutionCheck pipettesBriefly centrifuge standards anddissolve the powder thoroughly bygently mixingLow signal Too brief incubation timesInadequate reagentvolumes or improperdilutionEnsure sufficient incubation time.Assay procedure step 2 may bedone overnightCheck pipettes and ensure correctpreparationLarge CV Uneven pipettingBubbles present in wellsCheck pipettesLightly tap or use pipette tip todislodge from bottom of wellHigh background Plate is insufficientlywashedContaminated washbufferImproper TmReview the manual for proper wash.If using a plate washer, ensure thatall ports are unobstructed.Make fresh wash bufferCheck run parameters and calibrateinstrumentLow sensitivity Improper storage of theIQELISA kitImproper TmStore your standard at <-20°C afterreconstitution, others at 4°C.Check run parameters and calibrateinstrumentThis product is for research use only.©2019 RayBiotech, Inc11。
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Laser Marking Additive LaserAT-8632 Principle of Laser Marking
A pulsed laser beam of high energy is generated by laser generators. Laser marking additives make the light convert into the heat energy when the beam acting on the materials to be marked. At the same time, their surface is melted, discolored or even gasified, thereby forming a mark.
Features of Laser Marking
●Non-contact processing, durability;
●High precision, fast, high legibility, reliability;
●Forming a top-quality micro mark;
●Environment friendly;
●Easy to use, strong security features;
●Strong traceability of products;
●High-speed automatic processing can be achieved;
●The overall production cost of individual parts is far less than that of printing traditional
inks.
Roles Played by LaserAT-8632
LaserAT-8632 is a necessary additive for plastics, elastomers, and rubbers, which cannot be marked or weak marked by lasers. The marks produced by LaserAT-8632 are always clear, good and durable, and these marks cannot be gradually faded away by physical or chemical actions.
Application Areas
LaserAT-8632 is suitable to apply to mark the dark color on the light-colored plastics, elastomers, and rubbers.
Highlights
●The color of plastics, elastomers, and rubbers does not alter obviously after adding
LaserAT-8632.
● A high precision marking can be achieved, such as a photo-level.
Suitable Materials for LaserAT-8632
PP, PE, PC, PA6, PA66, ABS, PS, PBT, PET, PVC, POM, SEBS, TPU, TPE, TPV, and so
on.
Laser Marking Systems
Systems of the wavelength at 355-1064 nm can be used, as well as the wavelength at
10600nm (CO2 lasers). YAG and fiber laser marking systems (355-1064 nm) are strongly recommended.
Technical Data of LaserAT-8632
Parameters Typical values Test methods
Form Granule By
eyes Color White or light gray By eyes
Melt flowing rate
(g/10min,190 ºC,5kg) 15.0-25.0 ISO
1133:1997
Density (g/cm3) 1.3-2.1 ISO
1183-1:2004 Suitable laser wavelength (nm) 355-1064,10600 Internal test methods Package Size (kg) 1.0,25.0 ---
Processing
●LaserAT-8632 is recommended to compound with the target materials using extruders.
Processing parameters of the target materials remains unchanged during extrusion
granulation. Then blow molding, injection molding, extrusion or other technology can be
used to produce plastic parts.
●The plastic parts can be direct produced by injection molding, after a simple dry blend of
LaserAT-8632 and the target materials.
●During extrusion granulation and direct injection molding, LaserAT-8632 can be used
together with color masterbatch, dyes, and pigments of white, yellow (light), blue (light), red (light), gray, etc.
Dosage
●0.4-4 wt%, depending on the degree of the dark color of marks;
●In general, 1.0-2.5 wt% is always recommended.
Toxicity
LaserAT-8632 is no danger to human, and it’s environment friendly.
Package and Storage
●LaserAT-8632 is packaged by a plastic box or a carton lined with a PE bag;
●LaserAT-8632 is non-dangerous goods;
●Please store in dry and ventilated conditions;
●Waterproof and moisture-proof;
●Avoid sun exposure;
●Please seal the unused portion of LaserAT-8632;
●Please use up within 24 months.
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