Biological Therapeutics, Cell Culture Supernatant, Purified Protein
最低检测浓度
6.25 ng/mL
原理
ELISA Kit for the quantitative Measurement of host cell protein (HCP) residues in biopharmaceuticals by Pichia Pastoris (Strain X-33 and Derivatives) expression systems
Analytical Method
Quantitative
交叉反应 (详细)
No cross-reaction exists between the homologous antigens.
灵敏度
1.56 ng/mL
产品特性
This ELISA kit is applied to the solid phase sandwich Enzyme-Linked Immunosorbent Assay. The microplate has been pre-coated with a capture antibody. The antigen to be measured and the HRP-conjugated detection antibody are then added to the microplate wells sequentially to form a capture antibody-antigen-detection antibody complex. After washing, the conjugates uninvolved in the reaction are removed, and then a TMB substrate solution is added to the wells to incubate. TMB substrate solution turns blue after the oxidation of HRP and finally turns yellow immediately after adding the stop solution. The color of the TMB substrate positively correlated with the antigen bound in the initial steps. Measure the absorbance (OD value) at 450nm using a microplate reader, and create a standard curve along with the corresponding concentrations. Then, by inputting the OD values of the samples into the standard curve equation, calculate the concentration of the target protein in the sample.
Optimal working dilution should be determined by the investigator.
样本量
100 µL
实验时间
3.5 h
板类型
Pre-coated
实验流程
This ELISA kit is applied to the solid phase sandwich Enzyme-Linked Immunosorbent Assay. The microplate has been pre-coated with a capture antibody. The antigen to be measured and the HRP-conjugated detection antibody are then added to the microplate wells sequentially to form a capture antibody-antigen-detection antibody complex. After washing, the conjugates uninvolved in the reaction are removed, and then a TMB substrate solution is added to the wells to incubate. TMB substrate solution turns blue after the oxidation of HRP and finally turns yellow immediately after adding the stop solution. The color of the TMB substrate positively correlated with the antigen bound in the initial steps. Measure the absorbance (OD value) at 450nm using a microplate reader, and create a standard curve along with the corresponding concentrations. Then, by in putting the ODvalues of the samples into the standard curve equation, calculate the concentration of the target protein in the sample.