本试剂盒只能用于科学研究，不得用于医学诊断
检测原理
试剂盒采用双抗体一步夹心法酶联免疫吸附试验(ELISA)。往预先包被抗凝血素抗体IgM(CPT-IgM)的包被微孔中,依次加入标本、标准品、HRP标记的检测抗体,经过温育并洗涤。用底物TMB显色,TMB在化物酶的催化下转化成蓝色,并在酸的作用下转化成最终的黄色。颜色的深浅和样品中的抗凝血素抗体IgM(PT-IgM)呈正相关。用酶标仪在450nm 波长下测定吸光度(OD 值),计算样品浓度。
样品收集、处理及保存方法
1.  血清：使用不含热原和内毒素的试管，操作过程中避免任何细胞刺激，收集血液后，3000转离心10分钟将血清和红细胞迅速小心地分离。
2.  血浆：EDTA、柠檬酸盐或肝素抗凝。3000转离心30分钟取上清。
3.  细胞上清液：3000转离心10分钟去除颗粒和聚合物。
4.  组织匀浆：将组织加入适量生理盐水捣碎。3000转离心10分钟取上清。
5.  保存：如果样本收集后不及时检测，请按一次用量分装，冻存于-20℃，避免反复冻融，在室温下解冻并确保样品均匀地充分解冻。
自备物品
1.酶标仪（450nm）
2.高精度加样器及枪头：0.5-10uL、2-20uL、20-200uL、200-1000uL
3.37℃恒温箱
操作注意事项
1.  试剂盒保存在2-8℃，使用前室温平衡20分钟。从冰箱取出的浓缩洗涤液会有结晶，这属于正常现象，水浴加热使结晶完全溶解后再使用。
2.  实验中不用的板条应立即放回自封袋中，密封（低温干燥）保存。
3.  浓度为0的S0号标准品即可视为阴性对照或者空白；按照说明书操作时样本已经稀释5倍，最终结果乘以5才是样本实际浓度。
4.  严格按照说明书中标明的时间、加液量及顺序进行温育操作。
5.  所有液体组分使用前充分摇匀。
试剂盒组成

名称	96孔配置	48孔配置	备注
微孔酶标板	12孔×8条	12孔×4条	无
标准品	0.3mL*6管	0.3mL*6管	无
样本稀释液	6mL	3mL	无
检测抗体-HRP	10mL	5mL	无
20×洗涤缓冲液	25mL	15mL	按说明书进行稀释
底物A	6mL	3mL	无
底物B	6mL	3mL	无
终止液	6mL	3mL	无
封板膜	2张	2张	无
说明书	1份	1份	无
自封袋	1个	1个	无

注：标准品（S0-S5）浓度依次为：0、30、60、120、240、480 μg/mL
试剂的准备
 20×洗涤缓冲液的稀释：蒸馏水按1：20稀释，即1份的20×洗涤缓冲液加19份的蒸馏水。
洗板方法
1.  手工洗板：甩尽孔内液体，每孔加满洗涤液，静置1min后甩尽孔内液体，在吸水纸上拍干，如此洗板5次。
2.  自动洗板机：每孔注入洗液350μL，浸泡1min，洗板5次。
操作步骤
1.  从室温平衡20min后的铝箔袋中取出所需板条，剩余板条用自封袋密封放回4℃。
2.  设置标准品孔和样本孔，标准品孔各加不同浓度的标准品50μL；
3.  样本孔先加待测样本10μL，再加样本稀释液40μL；空白孔不加。 
4.  除空白孔外，标准品孔和样本孔中每孔加入辣根化物酶（HRP）标记的检测抗体100μL，用封板膜封住反应孔，37℃水浴锅或恒温箱温育60min。
  弃去液体，吸水纸上拍干，每孔加满洗涤液，静置1min，甩去5.洗涤液，吸水纸上拍干，如此重复洗板5次（也可用洗板机洗板）。
6.  每孔加入底物A、B各50μL，37℃避光孵育15min。
7.  每孔加入终止液50μL，15min内，在450nm波长处测定各孔的OD值。
结果判断
 绘制标准曲线：在Excel工作表中，以标准品浓度作横坐标，对应OD值作纵坐标，绘制出标准品线性回归曲线，按曲线方程计算各样本浓度值。

【点】
试剂盒性能

1. 准确性：标准品线性回归与预期浓度相关系数R值，大于等于0.9900。
2. 灵敏度：检测浓度小于1.0 μg/mL。
3. 特：不与其它可溶性结构类似物交叉反应。
4. 重复性：板内、板间变异系数均小于15%。
5. 贮藏：2-8℃，避光防潮保存。
6. 有效期：6个月
免责声明
1.  试剂盒仅供研究使用，不得用于临床实验或实验，否则所产生的一切后果，由实验者承担，本公司概不负责。
2.  严格按照说明书操作，实验者违反说明书操作，后果由实验者承担。


FOR RESEARCH USE ONLY. 
NOT FOR USE IN DIAGNOSTIC PROCEDURES.



Intended use
This PT-IgM ELISA kit is intended Laboratory for Research use only and is not for use in diagnostic or therapeutic procedures.The Stop Solution changes the color from blue to yellow and the intensity of the color is measured at 450 nm using a spectrophotometer. In order to measure the concentration of PT-IgM in the sample, this PT-IgM ELISA Kit includes a set of calibration standards. The calibration standards are assayed at the same time as the samples and allow the operator to produce a standard curve of Optical Density versus PT-IgM concentration. The concentration of PT-IgM in the samples is then determined by comparing the O.D. of the samples to the standard curve.
Sample collection and storages
Serum - Use a serum separator tube and allow samples to clot for 30 minutesbefore centrifugation for 10 minutes at approximately 3000×g. Remove serum and assay immediately or aliquot and store samples at -20℃ or -80℃.Avoid repeated freeze-thaw cycles
Plasma - Collect plasma using EDTA or heparin as an anticoagulant. Centrifuge samples for 30 minutes at 3000×g at 2-8℃ within 30 minutes of collection. Store samples at -20℃or -80℃. Avoid repeated freeze-thaw cycles.
 Cell culture supernates and other biological fluids - Remove particulates by centrifugation and assay immediately or aliquot and store samples at -20℃or -80℃. Avoid repeated freeze-thaw cycles. 
【示警】Note:  The samples shoule be centrifugated dequately and no hemolysis or granule was allowed.
Materials required but not supplied
1.  Standard microplate reader(450nm)
2.  Precision pipettes and Disposable pipette tips.
3.  37 ℃ incubator
Precautions
1.  Do not substitute reagents from one kit to another. Standard, conjugate and microplates are matched for optimal performance. Use only the reagents supplied by manufacturer.
2.  Do not remove microplate from the storage bag until needed. Unused strips should be stored at 2-8°C in their pouch with the desiccant provided.
3.  Mix all reagents before using.
Remove all kit reagents from refrigerator and allow them to reach room temperature ( 20-25°C) Materials supplied

Name	96 determinations	48 determinations
Microelisa stripplate	12*8strips	12*4strips
Standard	0.3ml*6tubes	0.3ml*6tubes
Sample Diluent	6.0ml	3.0ml
HRP-Conjugate reagent	10.0ml	5.0ml
20X Wash solution	25ml	15ml
Chromogen Solution A	6.0ml	3.0ml
Chromogen Solution B	6.0ml	3.0ml
Stop Solution	6.0ml	3.0ml
Closure plate membrane	2	2
User manual	1	1
Sealed bags	1	1

Note: Standard (S0 → S5) concentration was followed by:0,30,60,120,240,480 μg/mL
Reagent preparation
20×wash solution:Dilute with Distilled or deionized water 1:20.
Assay procedure
1.  Prepare all reagents before starting assay procedure. It is recommended that all Standards and Samples be added in duplicate to the Microelisa Stripplate.
2.  Add standard: Set Standard wells, testing sample wells. Add standard 50μl to standard well.
3.  Add Sample: Add testing sample 10μl then add Sample Diluent 40μl to testing sample well; Blank well doesn’t add anyting.
4.  Add 100μl of HRP-conjugate reagent to each well, cover with an adhesive strip and incubate for 60 minutes at 37°C. 
5.  Aspirate each well and wash, repeating the process four times for a total of five washes. Wash by filling each well with Wash Solution (400μl) using a squirt bottle, manifold dispenser or autowasher. Complete removal of liquid at each step is essential to good performance. After the last wash, remove any remaining Wash Solution by aspirating or decanting. Invert the plate and blot it against clean paper towels.
6.  Add chromogen solution A 50μl and chromogen solution B 50μl to each well. Gently mix and incubate for 15 minutes at 37°C. Protect from light.
7.  Add 50μl Stop Solution to each well. The color in the wells should change from blue to yellow. If the color in the wells is green or the color change does not 
appear uniform, gently tap the plate to ensure thorough mixing.
8.  Read the Optical Density (O.D.) at 450 nm using a microtiter plate reader within 15 minutes.
 Calculation of results
1.This standard curve is used to determine the amount in an unknown sample. The standard curve is generated by plotting the erage O.D. (450 nm) obtained for each of the six standard concentrations on the vertical (Y) axis versus the corresponding concentration on the horizontal (X) axis. 
2.First, calculate the mean O.D. value for each standard and sample. All O.D. values, are subtracted by the mean value of the zero standard before result interpretation. Construct the standard curve using graph paper or statistical software. 
3.To determine the amount in each sample, first locate the O.D. value on the Y-axis and extend a horizontal line to the standard curve. At the point of intersection, draw a vertical line to the X-axis and read the corresponding concentration. 
4.Any variation in operator, pipetting and washing technique, incubation time or temperature, and kit age can cause variation in result. Each user should obtain their own standard curve.
5.The sensitivity by this assay is 1.0 μg/mL
6.Standard curve
【点】

Storage：  2-8℃.

validity： six months.

FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS! PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE BEGINNING!

其它昆虫Elisa相关推荐：
KKX-57339M 小鼠糖链抗原125(CA125)elisa试剂盒 Mouse Carbohydrate Antigen 125 elisa kit CA125
KKX-58002M 小鼠自噬相关蛋白5(ATG5)elisa试剂盒 Mouse Autophagy Related Protein 5 elisa kit ATG5
KKX-57808M 小鼠日本病毒IgG抗体(JEV-IgG Ab)elisa试剂盒 Mouse Mouse Japanese encephalitis virus IgG antibody elisa kit JEV-IgG Ab
KKX-56463M 小鼠脂肪因子(Chemerin)elisa试剂盒 Mouse chemerin elisa kit Chemerin
KKX-56611M 小鼠半胱氨酸蛋白酶3(Casp-3)elisa试剂盒 Mouse Caspase 3 elisa kit Casp-3
KKX-58076M 小鼠27kDa热休克蛋白(Hsp27)elisa试剂盒 Mouse Heat Shock Protein 27 elisa kit Hsp27
KKX-45860Z 植物线粒体呼吸链复合物IV(MRCC Iv)elisa试剂盒 Plant mitochondrial respiratory chain complex IV elisa Kit
KKX-45676Z 植物轻型黄边病毒(MYEV)elisa试剂盒 Plant mild yellow edge virus elisa Kit
KKX-46667Z 植物脱氢奎尼酸合成酶(DHQS)elisa试剂盒 Plant dehydroquinate synthase elisa Kit
KKX-45672Z 植物雪花莲凝集素(GNA)elisa试剂盒 Plant GNA elisa Kit
KKX-58823M 小鼠抗猫细小病毒抗体(PV-Ab)elisa试剂盒 Mouse 不发说明书，仅供下单 elisa kit PV-Ab
KKX-59175M 小鼠血清肌酸酐(SC)elisa试剂盒 Mouse serum creatinine elisa kit SC
KKX-57404M 小鼠谷胱甘肽还原酶(GR)elisa试剂盒 Mouse Glutathione reductase elisa kit GR
KKX-59289M 小鼠羟自由基(OH)elisa试剂盒 Mouse Hydroxyl free radical elisa kit OH
KKX-56718M 小鼠肝再生增强因子(ALR)elisa试剂盒 Mouse augmenter of liver regeneration elisa kit ALR
KKX-56913M 小鼠卵清蛋白特IgE抗体(OVA-sIgE)elisa试剂盒 Mouse ovalbumin specific IgE elisa kit OVA-sIgE
KKX-57027M 小鼠(GH)elisa试剂盒 Mouse growth hormone elisa kit GH
KKX-58020M 小鼠白介素2可溶性受体α链(sIL-2Rα CD25)elisa试剂盒 Mouse soluble interleukin-2 receptor,sIL-2Rα elisa kit sIL-2Rα CD25
KKX-59207M 小鼠纤溶酶(plasmin)elisa试剂盒 Mouse plasmin elisa kit plasmin
KKX-57551M 小鼠可溶性内皮细胞粘附分子1(sVCAM-1)elisa试剂盒 Mouse soluble Vascuolar cell adhesion molecule 1 elisa kit sVCAM-1
KKX-45685Z 植物NADP-依赖苹果酸脱氢酶(NADP-DMD)elisa试剂盒 Plant NADP-dependent malate dehydrogenase elisa Kit
KKX-46428Z 植物玉米黄质化酶(ZEP)elisa试剂盒 Plant Zeaxanthin epoxidase elisa Kit
KKX-58845M 小鼠芳香胺-N-基转移酶(AANAT)elisa试剂盒 Mouse Aromatic amine N-acetyltransferase elisa kit AANAT
KKX-46077Z 植物磷酸苷油酸脱氢酶(GADPH)elisa试剂盒 Plant Glyceric acid phosphate dehydrogenase elisa Kit
KKX-57658M 小鼠抗猪圆环病毒抗体(PCV-Ab)elisa试剂盒 Mouse Porcine circovirus antibody elisa kit PCV-Ab
KKX-58994M 小鼠受体β(IR-β)elisa试剂盒 Mouse insulin receptor β elisa kit IR-β
KKX-57320M 小鼠磷酸胆碱(PC)elisa试剂盒 Mouse Phosphorylcholine elisa kit PC
KKX-45650Z 植物7-乙氧基-3-异吩恶唑酮-脱酶(EROD)elisa试剂盒 Plant 7-ethoxyresorufin O-deethylase elisa Kit
KKX-57177M 小鼠血小板型磷酸果糖激酶(PFKP)elisa试剂盒 Mouse phosphofructokinase-platelet elisa kit PFKP
KKX-58152M 小鼠氧化型辅酶II(NADP)elisa试剂盒 Mouse NADP elisa kit NADP
KKX-59121M 小鼠血小板内皮细胞粘附分子6(PECAM6)elisa试剂盒 Mouse Platelet;Endothelial Cell Adhesion Molecule 6 elisa kit PECAM6
KKX-56857M 小鼠肽(cathelicidin)elisa试剂盒 Mouse cathelicidin elisa kit cathelicidin