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Mouse sTNF RI ELISA Kit(TNFRSF1A) (RMEK-0153960)

Cat. No.: RMEK-0153960

Category: ELISA Kits

INQUIRY 1 x 96 tests
Mouse sTNF RI ELISA Kit (TNFRSF1A) is a single-wash 90 min sandwich ELISA designed for the quantitative measurement of sTNF RI (TNFRSF1A) protein in cell culture supernatant, cit plasma, edta plasma, serum, and urine. The technology employs capture antibodies conjugated to an affinity tag that is recognized by the monoclonal antibody used to coat our plates. This approach to sandwich ELISA allows the formation of the antibody-analyte sandwich complex in a single step, significantly reducing assay time.

Product Features

Species Reactivity Mouse
Detection Method Colorimetric
Assay Duration One step assay
Assay Time 1.5 h
Assay Type Sandwich (quantitative)
Precision Intra-Assay-Serum-5-1.5%; Inter-Assay-Serum-3-13.8%
Sensitivity 1.2 pg/mL
Range 7.81 pg/mL - 500 pg/mL
Sample Type Cell culture supernatant, Cit plasma, EDTA Plasma, Serum, Urine
Recovery Urine-103-101% - 109%; Serum-113-107% - 118%; Cell culture media-95-94% - 95%; EDTA Plasma-102-97% - 109%; Cit plasma-106-97% - 112%
Key Features One-wash 90 minute protocol; Sensitivity: 1.2 pg/mL; Range: 7.81 pg/mL - 500 pg/mL; Sample type: Cell culture supernatant, Cit plasma, EDTA Plasma, Serum, Urine; Detection method: Colorimetric; Assay type: Sandwich (quantitative); Reacts with: Mouse

Target Information

Target Symbol sTNF RI
Function Receptor for TNFSF2/TNF-alpha and homotrimeric TNFSF1/lymphotoxin-alpha. The adapter molecule FADD recruits caspase-8 to the activated receptor. The resulting death-inducing signaling complex (DISC) performs caspase-8 proteolytic activation which initiates the subsequent cascade of caspases (aspartate-specific cysteine proteases) mediating apoptosis. Contributes to the induction of non-cytocidal TNF effects including anti-viral state and activation of the acid sphingomyelinase.
Cellular Localization Cell membrane. Golgi apparatus membrane. Secreted. A secreted form is produced through proteolytic processing and Secreted. Lacks a Golgi-retention motif, is not membrane bound and therefore is secreted.
Domain The domain that induces A-SMASE is probably identical to the death domain. The N-SMASE activation domain (NSD) is both necessary and sufficient for activation of N-SMASE.Both the cytoplasmic membrane-proximal region and the C-terminal region containing the death domain are involved in the interaction with TRPC4AP.
Post-transcriptional Modifications The soluble form is produced from the membrane form by proteolytic processing.
Involvement in Disease Familial hibernian feverMultiple sclerosis 5

Storage & Shipping

Storage Store at 2-8°C
Shipping Gel Packs
Stability The stability of 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.

For research use only. Not for clinical use.