Sandwich ELISA (enzyme-linked immunosorbent assay) kit
ZG16B, EECP, PAUF, JCLN2, HRPE773
Intended Sample Types
Plasma, Serum, Tissue Homogenates
96-Well Strip Plate
Colorimetric - 450nm (TMB)
0.312 - 20 ng/ml
Intra-Assay: CV<8% Inter-Assay: CV<10%
Store at 4°C. Stable for 6 months.
Due to their limited shelf life, LSBio ELISA kits are not typically stocked as finished goods. Upon receipt of an order each kit is assembled and tested to ensure that it meets specifications before shipping. Minor changes may occur to the Range, Sensitivity, and Precision. In the event of a significant change the order would be confirmed with the customer before shipping ELISA kit lot numbers reflect the date of final assembly and testing for each specific kit rather than a bulk manufactured lot. All kits are tested to confirm that they fall within their defined Inter- and Intra- assay coefficient of variation.
- Adhesive Plate Sealers
- Coated 96-well Strip Plate
- Detection Antibody Diluent
- Biotinylated Detection Antibody (100x)
- HRP-Streptavidin Conjugate (100x)
- HRP-Streptavidin Conjugate Diluent
- Sample Diluent
- TMB Substrate
- Stop Solution
- Wash Buffer (25x)
- Standard (Lyophilized)
This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Anti- ZG16Bantibody was pre-coated onto 96-well plates. And the biotin conjugated anti- ZG16B antibody was used as detection antibodies. The standards, test samples and biotin conjugated detection antibody were added to the wells subsequently, and wash with wash buffer. HRP- Streptavidin was added and unbound conjugates were washed away with wash buffer. TMB substrates were used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the ZG16B amount of sample captured in plate. Read the O.D. absorbance at 450nm in a microplate reader, and then the concentration of ZG16B can be calculated.
For research use only.