Components | Shipping Condition | Unit Size | Detection Method |
P.pastoris Calibration Standard | 2-8℃ | 96 Tests | Sandwich ELISA |
Anti-P.pastoris HCP Microtiter Strips | |||
Reconstitution Solution | |||
Diluent | |||
Wash Buffer Concentrate (10×) | |||
Anti-P.pastoris:HRP (100×) | |||
TMB Substrate | |||
Stop Solution | |||
Sealing Film |
This kit is based on the solid-phase enzyme-linked immunosorbent assay (ELISA) with a double-antibody sandwich technique to detect residual host cell proteins (HCPs) from P.pastoris cells. A sheep polyclonal antibody specific to P.pastoris HCPs was employed in the assay to capture any remaining HCPs in the sample. The antibody coverage is assessed by the current mainstream method. Both the Calibration Standard (or test sample) and the HRP (Horseradish Peroxidase) labeled with anti-P.pastoris HCP antibody were simultaneously added to the microtiter plate coated with the affinity purified capture antibody, and followed by incubation and washing. Then TMB (3,3',5,5' -tetramethylbenzidine) substrate was added into reaction, HRP catalyzed the oxidation of TMB by H2O2 to produce a blue colored product (maximum absorption peak at 655 nm). Then the stop solution was added to terminate the enzymatic reaction, resulting in a yellow colored product (maximum absorption peak at 450 nm). The absorbance values at 450 nm wavelength was positively correlated with the HCPs concentration in the Calibration Standard and the samples. The concentration of HCPs in the samples can be calculated using a dose-response curve.
Linearity & Range | 2-200 ng/mL, R2>0.990 |
Accuracy | Recovery Rate= 97.7%-110.2% |
LLOQ | 2 ng/mL |
LOD | 0.5 ng/mL |
Repeatability | 6.6%-8.0% (CV≤20%) |
Antibody Coverage (IMBS-2D) | 72.1%-96.0% |
Antibody Coverage (IMBS-LC/MS) | 99.2% |
Robustness | Instrument suitability not limited toThermo Multiskan FC and MD Spectra Max ABS |
SHENTEK® Residual Host Cell DNA Sample Preparation Kit
SHENTEK® Residual Pichia pastoris DNA Quantitation Kit