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IL-18Rα ELISA Kit

  • Product Information
  • Description
Catalog: C-EL-1818T
Product Type: Test kit
Size: 96 tests
Principle: Solid Phase Sandwich ELISA
Conjugation: HRP
Species: Mouse
Detection range: 18.75-1200 pg/mL
Sensitivity: 6.06 pg/mL
Specificity: Recognizes both recombinant and natural Mouse IL-18Rα
Interference: Preparations a series of mouse IL18 in a mid-range recombinant mouse IL18R1 control were assayed for interference. Interference was observed at concentrations 6 ng/mL.
Sample type: Lysate
Test type: Quantitative
Analysis mode: ELISA
Shipping: This ELISA Kit is shipped at ambient temperature.
Storage: 2-8℃
Full name: interleukin 18 receptor 1
Application: Neuroinflammation

This IL-18Rα ELISA Kit, Mouse is an enzyme-linked immunosorbent assay for the quantitative measurement of Mouse IL-18Rα protein in Lysate . It contains recombinant Mouse IL-18Rα, and antibodies raised against the recombinant protein. This ELISA kit is complete and ready-to-use.Interleukin-18 receptor 1 (IL18R1) also known as CD218 antigen-like family member A, CDw218a, IL1 receptor-related protein, and CD218a, is an interleukin receptor of the immunoglobulin superfamily. IL18R1 is found expressed in the lung, leukocytes, spleen, liver, thymus, prostate, small intestine, colon, placenta, and heart, and is absent from the brain, skeletal muscle, pancreas, and kidney. A high level of expression is found in Hodgkin disease cell lines. This receptor is specifically bound to interleukin 18 (IL18) and is essential for IL18 mediated signal transduction. IL18R1 contains 3 Ig-like C2-type (immunoglobulin-like) domains and 1 TIR domain. It is a single-pass type I membrane protein. IFN-alpha and IL12 are reported to induce the expression of this receptor in NK and T cells. The increased expression of IL18R1 may contribute pathogenically to disease and is therefore a potential therapeutic target. The absence of a genetic association in the IL18R1 gene itself suggests regulation from other parts of the genome, or as part of the inflammatory cascade in multiple sclerosis without a prime genetic cause.

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