Mouse Toll/Interleukin-1 receptor domain-containing adapter protein (TIRAP) ELISA Kit | AE14926MO

Mouse Toll/Interleukin-1 receptor domain-containing adapter protein (TIRAP) ELISA Kit | AE14926MO | Gentaur UK, US & Europe Distribution

Species Reactivity: Mouse (Mus musculus)

Abbreviation: TIRAP

Alternative Name: FLJ42305; Mal; wyatt; MyD88 adapter-like protein|OTTHUMP00000179130|Toll-interleukin 1 receptor domain-containing adaptor protein|Toll-like receptor adaptor protein|adapter protein wyatt

Application: ELISA

Range: 0.312-20 ng/mL

Sensitivity: 0.109 ng/mL

Intra-Assay: ≤6.3%

Inter-Assay: ≤7.3%

Recovery: 1, 09

Sample Type: Serum, Plasma, Other biological fluids

Detection Method: Sandwich

Analysis Method : Quantitive

Test Principale: This assay employs a two-site sandwich ELISA to quantitate TIRAP in samples. An antibody specific for TIRAP has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyTIRAP present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for TIRAP is added to the wells. After washing, Streptavidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of TIRAP bound in the initial step. The color development is stopped and the intensity of the color is measured.

Product Overview: TIRAP is a TIR adaptor protein involved in the TLR4 signaling pathway of the immune system. It activates NF-kappa-B, MAPK1, MAPK3 and JNK, which then results in cytokine secretion and the inflammatory response. Alternative splicing of this gene results in several transcript variants; however, not all variants have been fully described. MAL, unlike MYD88, does not interact with IRAK1 and is not inhibited by the dominant-negative N-terminal region of IRAK1; however, like MYD88, MAL does, through its TIR domain, interact with and is inhibited in NFKB activation by the dominant-negative form of IRAK2. A dominant-negative form of MAL inhibits TLR4 or lipopolysaccharide activation of NFKB, but not NFKB activation by IL1R1 or IL18R. Immunoprecipitation analysis showed that TLR4 and MAL are constitutively associated.

Stability: The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calculated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C) .