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Trypsin Like Enzyme ELISA Kit
Product Introduction
In December 2022, the National Institutes for Food and Drug Control published a research paper titled "Establishment and Validation of a Double-antibody Sandwich Quantitative ELISA for TrypLE" in Chinese Journal of Biologicals. Junyan Biotech participated in the publication of this article. In this study, orthogonal experiments were used to determine the optimal concentrations of the capture antibody and detection antibody. A double - antibody sandwich quantitative ELISA method for TrypLE was established and verified for its linear range, specificity, limit of detection, limit of quantification, accuracy, and repeatability. The applicability of the method was verified by detecting various biological products using the established method.
After strict methodological verification, Junyan Biotech independently developed an ELISA - based recombinant trypsin - like analogue quantitative detection kit, which can accurately identify multiple imported and domestic recombinant trypsins and their analogues, including TrypLE™ from Gibco.
The Recombinant Trypsin - like Analogue Quantitative Detection Kit (Catalog No. KET01 - 96) can quickly and effectively detect the residual amount of TrypLE™ in various samples. For stem cell users, Junyan Biotech has launched a second - generation product (Catalog No. KET02 - 96), which has lower sensitivity (the limit of quantification is as low as 0.1 ng/mL) to better meet diverse detection needs.
Advantages and Features
Performance Indicators
Data Results
Detection Principle
This kit uses the double - antibody sandwich enzyme - linked immunosorbent assay (ELISA) technology to determine the trace residual amount of TrypLE™ in samples. The 96 - well microplate is coated with a capture antibody to form a solid - phase antibody. Then, standard products and test samples are added, followed by a detection antibody labeled with horseradish peroxidase (HRP). A sandwich complex of solid - phase antibody - TrypLE™ - labeled antibody is formed. After the reaction, the plate is washed, and then a substrate is added for a color - development reaction. The substrate is converted into blue under the catalysis of HRP and then into yellow under the action of a stop solution (as shown in the figure below). The absorbance (OD value) is measured at a wavelength of 450 nm, and the content of TrypLE in the test sample is calculated through the standard curve.
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