KGF/FGF7 (Keratinocyte Growth Factor) (KGF/FGF7) ELISA Kit for Rabbit

Principle of the Assay: This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Anti- KGF/FGF7 antibody was pre-coated onto 96-well plates. And the biotin conjugated anti- KGF/FGF7 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 KGF/FGF7 amount of sample captured in plate. Read the O.D. absorbance at 450nm in a microplate reader, and then the concentration of KGF/FGF7 can be calculated.

Small volumes of KGF/FGF7 elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

MBS766215 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the KGF/FGF7 (Keratinocyte Growth Factor) ELISA Kit target analytes in biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing KGF/FGF7. The ELISA analytical biochemical technique of the MBS766215 kit is based on KGF/FGF7 antibody-KGF/FGF7 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect KGF/FGF7 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, KGF/FGF7. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).