Catalog: | C-EL-1817T |
Product Type: | Test kit |
Size: | 96 tests |
Principle: | Solid Phase Sandwich ELISA |
Conjugation: | HRP |
Species: | Human |
Detection range: | 7.81-500 pg/mL |
Sensitivity: | 3.49 pg/mL |
Specificity: | Recognizes both recombinant and natural Human IL-18Rα |
Interference: | Preparations of IL18 prepared at 5 ng/mL in a mid-range recombinant human IL18R1 control was assayed for interference. No significant interference was observed. |
Sample type: | Serum |
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, Human is an enzyme-linked immunosorbent assay for the quantitative measurement of Human IL-18Rα protein in Serum . It contains recombinant Human 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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