抗聚乙二醇(PEG)抗体ELISA试剂盒(小鼠IgG特异性)
货号:EL-141-PEG-mIGG
品牌:AffinityImmuno
产品特性
Anti-PEG antibody ELISA Kit (mouse IgG specific)
Reactivity:mouse
Application:Quantiification of mouse IgG specific
Methode type:Direct sandwich ELISA
Sample type:Serum and Plasma
规格 | 价格 |
---|---|
96 wells | ¥咨询 |
3 x 96 wells | ¥咨询 |
5 x 96 wells | ¥咨询 |
产品咨询:info@biopcr.com
产品订购:sales@biopcr.com
技术支持:tech@biopcr.com
服务热线:400-860-6200
详细介绍
产品名称:抗聚乙二醇(PEG)抗体ELISA试剂盒(小鼠IgG特异性)
别名:Mouse IgG antibodies to PEG ELISA;抗PEG抗体ELISA试剂盒(小鼠IgG特异性);抗聚乙二醇抗体ELISA试剂盒
抗原(Antigen):Anti-PEG mouse IgG antibodies
反应性(Reactivity):mouse
特异性(Specificity):Anti-PEG antibodies
应用(Application):Quantiification of mouse IgG specific
检测类型(Method type):Direct sandwich ELISA
检测方法(Detection Method):Peroxidase / OD450
检测精度(Assay precision):Intra-assay coefficient of variation (CV) <10%. Inter-assay CV was <10%
酶标板类型(Plate):Strip
样本类型(Sample type):Serum and Plasma
样本体积(Sample volume):15ul
检测时间(Assay time):2.5 hours
防腐剂(Preservative):none
试剂盒组分(Components):
Coated microtiter plate, 96 wells
QC samples - 6x250ul
10X wash buffer - 50 ml
Assay buffer - 50ml
1000X detection reagent - 17ul
TMB - 12ml
TMB stop solution - 12ml
Plate sealers - 3
运输条件(Shipping):Wet ice湿冰
储存(Storage):Stable at -20℃ for 1 year
抗聚乙二醇抗体ELISA试剂盒(小鼠IgG特异性),Anti-PEG antibody ELISA Kit (mouse IgG specific),本免疫原性检测采用直接ELISA技术,通过测定小鼠血清或血浆中与固定化聚乙二醇结合的IgG抗体,定性检测抗PEG IgG抗体的存在。
背景信息(Background information):
Polyethylene glycol (PEG) chains are often used to modify therapeutic biologic agents in order to prolong the circulating half-life of the modified protein. It has been reported that repeat injections of PEGylated proteins can induce anti-PEG antibodies.
检测原理(Summary of the assay):
This assay employs the sandwich enzyme immunoassay technique. Immobilized PEG is coated onto a 96 well microplate. Calibrator and test samples are pipetted into the appropriate wells. Anti-PEG antibodies present in biological matrices is bound by the immobilized PEG. After washing away any unbound substances, enzyme linked anti IgG or IgM antibody is added to the wells. The plate is washed to remove any unbound antibody-enzyme reagent and a substrate solution is added to the wells for color development. The color development is proportional to the amount of anti-PEG antibodies present in test samples. The color development is stopped and the intensity of the color is measured
样本采集(Sample collection):
This kit is compatible with EDTA-plasma, heparinplasma and serum samples. Samples can be stored at or below -20°C for up to 1 year.
样本制备(Sample preparation):
Dilute test samples 1/5 with assay buffer before use (for example add 50μl of test sample to 200μl assay buffer). Mix well.
试剂准备(Reagent preparation):
Prepare only the appropriate amount of required reagent on the day of use. Store all reagents as per instructions stated on the label.
1. Wash Buffer (1X) Preparation Dilute wash buffer concentrate with deionized water 1/10 before use (for example add 20mL concentrate to 180mL deionized water). Mix well.
2. Detection Reagent (1X) Preparation: Dilute detection reagent with assay buffer 1/1000 before use (for example add 11μl concentrate to 11ml of assay buffer). Mix well. The following is an example calibrator curve.
检测程序(Assay procedure):
This assay employs the sandwich enzyme immunoassay technique. Immobilized PEG is coated onto a 96 well microplate. Calibrator and test samples are pipetted into the appropriate wells. Anti-PEG antibodies present in biological matrices is bound by the immobilized PEG. After washing away any unbound substances, enzyme linked anti IgG or IgM antibody is added to the wells. The plate is washed to remove any unbound antibody-enzyme reagent and a substrate solution is added to the wells for color development. The color development is proportional to the amount of anti-PEG antibodies present in test samples. The color development is stopped and the intensity of the color is measured
结果计算(Results calculation):
1. Construct a standard curve by plotting the absorbance obtained from each standard against concentration. Use a 4 or 5 parameter curve fit. Alternatively a log-log curve fit may be used.
2. The concentration of the unknowns can be read directly from this standard curve using the absorbance value for each sample.
3. Any sample undiluted or diluted still reading greater than the highest standard should be diluted appropriately with assay buffer and retested. If the samples have been diluted, the concentration determined from the standard curve must be multiplied by the dilution factor.
[注意事项]:勃谱生物的抗聚乙二醇抗体ELISA试剂盒(抗PEG抗体ELISA试剂盒)-小鼠IgG特异性产品仅用于研究用途。不可用于诊断、医疗或其他用途。
[NOTICE]: Our products are for RESEARCH USE ONLY. Not for diagnostic, medical or other use.
返回列表
反应性(Reactivity):mouse
特异性(Specificity):Anti-PEG antibodies
应用(Application):Quantiification of mouse IgG specific
检测类型(Method type):Direct sandwich ELISA
检测方法(Detection Method):Peroxidase / OD450
检测精度(Assay precision):Intra-assay coefficient of variation (CV) <10%. Inter-assay CV was <10%
酶标板类型(Plate):Strip
样本类型(Sample type):Serum and Plasma
样本体积(Sample volume):15ul
检测时间(Assay time):2.5 hours
防腐剂(Preservative):none
试剂盒组分(Components):
Coated microtiter plate, 96 wells
QC samples - 6x250ul
10X wash buffer - 50 ml
Assay buffer - 50ml
1000X detection reagent - 17ul
TMB - 12ml
TMB stop solution - 12ml
Plate sealers - 3
运输条件(Shipping):Wet ice湿冰
储存(Storage):Stable at -20℃ for 1 year
抗聚乙二醇抗体ELISA试剂盒(小鼠IgG特异性),Anti-PEG antibody ELISA Kit (mouse IgG specific),本免疫原性检测采用直接ELISA技术,通过测定小鼠血清或血浆中与固定化聚乙二醇结合的IgG抗体,定性检测抗PEG IgG抗体的存在。
背景信息(Background information):
Polyethylene glycol (PEG) chains are often used to modify therapeutic biologic agents in order to prolong the circulating half-life of the modified protein. It has been reported that repeat injections of PEGylated proteins can induce anti-PEG antibodies.
检测原理(Summary of the assay):
This assay employs the sandwich enzyme immunoassay technique. Immobilized PEG is coated onto a 96 well microplate. Calibrator and test samples are pipetted into the appropriate wells. Anti-PEG antibodies present in biological matrices is bound by the immobilized PEG. After washing away any unbound substances, enzyme linked anti IgG or IgM antibody is added to the wells. The plate is washed to remove any unbound antibody-enzyme reagent and a substrate solution is added to the wells for color development. The color development is proportional to the amount of anti-PEG antibodies present in test samples. The color development is stopped and the intensity of the color is measured
样本采集(Sample collection):
This kit is compatible with EDTA-plasma, heparinplasma and serum samples. Samples can be stored at or below -20°C for up to 1 year.
样本制备(Sample preparation):
Dilute test samples 1/5 with assay buffer before use (for example add 50μl of test sample to 200μl assay buffer). Mix well.
试剂准备(Reagent preparation):
Prepare only the appropriate amount of required reagent on the day of use. Store all reagents as per instructions stated on the label.
1. Wash Buffer (1X) Preparation Dilute wash buffer concentrate with deionized water 1/10 before use (for example add 20mL concentrate to 180mL deionized water). Mix well.
2. Detection Reagent (1X) Preparation: Dilute detection reagent with assay buffer 1/1000 before use (for example add 11μl concentrate to 11ml of assay buffer). Mix well. The following is an example calibrator curve.
检测程序(Assay procedure):
This assay employs the sandwich enzyme immunoassay technique. Immobilized PEG is coated onto a 96 well microplate. Calibrator and test samples are pipetted into the appropriate wells. Anti-PEG antibodies present in biological matrices is bound by the immobilized PEG. After washing away any unbound substances, enzyme linked anti IgG or IgM antibody is added to the wells. The plate is washed to remove any unbound antibody-enzyme reagent and a substrate solution is added to the wells for color development. The color development is proportional to the amount of anti-PEG antibodies present in test samples. The color development is stopped and the intensity of the color is measured
结果计算(Results calculation):
1. Construct a standard curve by plotting the absorbance obtained from each standard against concentration. Use a 4 or 5 parameter curve fit. Alternatively a log-log curve fit may be used.
2. The concentration of the unknowns can be read directly from this standard curve using the absorbance value for each sample.
3. Any sample undiluted or diluted still reading greater than the highest standard should be diluted appropriately with assay buffer and retested. If the samples have been diluted, the concentration determined from the standard curve must be multiplied by the dilution factor.
[注意事项]:勃谱生物的抗聚乙二醇抗体ELISA试剂盒(抗PEG抗体ELISA试剂盒)-小鼠IgG特异性产品仅用于研究用途。不可用于诊断、医疗或其他用途。
[NOTICE]: Our products are for RESEARCH USE ONLY. Not for diagnostic, medical or other use.