Rat IL-6(Interleukin-6) ELISA Kit

Rat IL-6(Interleukin-6) ELISA Kit Basic Information 
Product Name: Rat IL-6(Interleukin-6) ELISA Kit
Catalog NO.: FY-ER3995
Alias: IL6 ELISA Kit, BSF2 ELISA Kit, HGF ELISA Kit, HSF ELISA Kit, IFNB2 ELISA Kit, CDF ELISA Kit
Application: IL-6 ELISA Kit allows for the in vitro quantitative determination of IL-6 concentrations in serum, plasma, tissue homogenates and other biological fluids.
Size: 48T, 96T
Storage: 2-8 ℃ for 6 months
Sensitivity: < 37.5pg/ml
Species: Rat
Uniprot: P20607
CV %（）
Intra-Assay: CV<8%
Inter-Assay: CV<10%
Note: For Research Use Only
Feiyue’s Rat IL-6 is an ELISA reagent for detection of IL-6 in serum, plasma or cell with sensitivity, specificity and consistency.

Rat IL-6(Interleukin-6) Introduciton
Interleukin-6, abbreviated as interleukin-6, was originally discovered by the team of Japanese immunologist Chuzo Kishimoto. It is an interleukin that mediates inflammation (but in some cases it also has an anti-inflammatory effect). Interleukin-6 can be secreted by T cells, B cells, monocytes, fibroblasts, keratinocytes, endothelial cells, mesangial cells, and some tumor cells. Interleukin-6 was originally thought to be a factor that can promote the differentiation of B cells into plasma cells, but other functions have been discovered later. For example, interleukin-6 can cross the blood-brain barrier, which is related to the normal physiological process of the central nervous system and the process of damage repair.

Rat IL-6(Interleukin-6) ELISA Kit Test method
This kit uses sandwich ELISA to detect the concentration of Rat IL-6.
Rat IL-6-specific monoclonal antibody has been pre-coated in the wells of the supplied microplate. Standards samples and controls are added to interact with the immobilized antibody. A sandwich complex is formed by additional anti-Rat IL-6 antibody with HRP-Streptavidin. TMB solution is added to react with the sandwich for ming optical signal measured by microplate reader. The concentration of Rat IL-6 in the sample can be calculated by comparing the absorbance of the sample with the standard curve.