
KRIBIOLISA Vero HCP (Algemene dekking) ELISA
Kwaliteit
ISO Gecertificeerd
Levering
24-48 uur
Technische Specificaties
The KRIBIOLISA Bioprocess Assay Kits available enable researchers to estimate and measure the amount of residual analyte left post downstream purification process. These assays can help identify or characterize the residual analyte which is important in early process and final product release. This Assay kit is designed to facilitate the identification and characterization of bioprocess analytes used in production and purification. Assay Features include: - Ready to use protocol with pre-coated breakapart wells for ease of use - Standardisation and High Reproducibility - Lot to Lot Consistency - Accuracy and Precision Validated against seven points for a Gold Ring Standard Quality - the benchmark sign for Krishgen quality. The kits are used for assessing the specific biomarker in samples analyte which may be cell culture supernatant and other biological preparations. Unlike competitor assays available, we offer pre-coated ready-to-use assays to ensure high level of reproducibility and accuracy and also offer custom assay development which is process specific to comply with FDA needs from our ISO13485 certified factory and labs.
Assay Range: 0.313 - 20 ng/ml | Sensitivity: 0.188 ng/ml Assay Range: | Sensitivity: Availability: 3 - 4 Weeks | Pack Size: 96 wells Availability: | Pack Size:
Double Antibody, Sandich ELISA
Sandwich ELISA, Double Antibody
Cell Culture Supernatant and other biological samples
0.313 - 20 ng/ml
0.188 ng/ml
Room Temperature / 2-8 Degrees Celsius
The kit and its components are to be stored as indicated in the IFU (instructions for use) . To ensure quality of your results, if all the wells in the kit are not being used, store the unused wells in the foil pouch containing the desiccant pack, well sealed and store at the indicated temperature.
The assay recognises host cell proteins including low and high molecular weight proteins.
Beschrijving
The KRIBIOLISA Bioprocess Assay Kits available enable researchers to estimate and measure the amount of residual analyte left post downstream purification proce
Specificaties
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