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Mouse IL-1ra/IL-1F3 ELISA Kit

  • Product Information
  • Description
Catalog: C-EL-2136T
Product Type: Test kit
Size: 96 tests
Principle: Sandwich ELISA
Species: Mouse
Detection range: 15.6-1000 pg/mL,7.8-500 pg/mL
Sensitivity: 3.0 pg/mL
Sample type: Serum, Plasma, Cell culture supernatants
Test type: Quantitative
Analysis mode: ELISA
Storage: All the reagents are stored at 2-8℃. Refer to the protocol for further storage instructions.
Synonyms:: F630041P17Rik, IL 1ra, IL-1F3, IL-1ra, Il1rn
Application: Interleukin 13 (IL-13) is an immunoregulatory cytokine produced primarily by activated Th2 cells. This cytokine is involved in several stages of B-cell maturation and differentiation. IL-13 up-regulates CD23 and MHC class II expression, and promotes IgE isotype switching of B cells. IL-13 inhibits the production of a series of cytokines like IL-1, IL-6, TNF-alpha, and IL-8 by activated human monocytes. IL-13 induces IFN-gamma production by NK cells. IL-13 is thought to be important cytokine in the pathogenesis of asthma, and more recently has been shown to play a pivotal role in a number of fibrotic diseases including hepatic and pulmonary fibrosis, and nodular sclerosing Hodgkin’s disease.

This test kit is a solid phase sandwich Enzyme Linked-Immuno-Sorbent Assay (Sandwich ELISA). The IL-1ra ELISA kit is to be used to detect and quantify protein levels of endogenous IL-1ra. The assay recognizes human,mouse and Rat IL-1ra. An antibody specific for IL-1ra has been pre-coated onto the microwells. The IL-1ra protein in samples is captured by the coated antibody after incubation. Following extensive washing, another antibody of biotinylated specific for IL-1ra is added to detect the captured IL-1ra protein. For signal development, Streptavidin-HRP is added, followed by Tetramethyl-benzidine (TMB) reagent. Solution containing sulfuric acid is used to stop color development and the color intensity which is proportional to the quantity of bound protein is measurable at 450 nm with the correction wavelength set at 630 nm.

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