Human TMEM173 ELISA Kit

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  • Alternative name

    Human hSTING ELISA Kit;Human endoplasmic reticulum interferon stimulator ELISA Kit;Human ERIS ELISA Kit;Human Mediator of IRF3 activation ELISA Kit;Human hMITA ELISA Kit;Human transmembrane protein 173 ELISA Kit;Human MITA ELISA Kit;Human MPYS ELISA Kit;Human NET23 ELISA Kit;Human SAVI ELISA Kit;Human STING ELISA Kit;Human stimulator of interferon genes protein ELISA Kit;Human N-terminal methionine-proline-tyrosine-serine plasma membrane tetraspanner ELISA Kit;Human endoplasmic reticulum IFN stimulator ELISA Kit;Human mitochondrial mediator of IRF3 activation ELISA Kit;

  • Catalog
    E039232
  • species
    Human
  • GeneTMEM173
  • Standard CurveHuman TMEM173 ELISA Kit
  • Other Species Mouse Tmem173 ELISA KitBovine TMEM173 ELISA KitChicken TMEM173 ELISA KitPorcine TMEM173 ELISA KitRat Tmem173 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of TMEM173. No significant cross-reactivity or interference between TMEM173 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between TMEM173 and all the analogues, therefore, cross reaction may still exist in some cases.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity0.1 ng/mL.
  • Intended UseHuman TMEM173 ELISA Kit allows for the in vitro quantitative determination of TMEM173 , concentrations in serum, Plasma , tissue homogenates and Cell culture supernates and Other biological fluids.
  • StorageStore the whole ELISA kit at 4℃
  • Product Description
    specifical
    Intended Uses: This TMEM173 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human TMEM173. This ELISA kit for research use only, not for therapeutic or diagnostic applications! Principle of the Assay||TMEM173 ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-TMEM173 antibody and an TMEM173-HRP conjugate. The assay sample and buffer are incubated together with TMEM173-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the TMEM173 concentration since TMEM173 from samples and TMEM173-HRP conjugate compete for the anti-TMEM173 antibody binding site. Since the number of sites is limited, as more sites are occupied by TMEM173 from the sample, fewer sites are left to bind TMEM173-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The TMEM173 concentration in each sample is interpolated from this standard curve.
  • Human Stimulator of interferon genes protein Protein information
  • Uniprot ID STING_HUMAN
  • Uniprot AC Q86WV6; A8K3P6; B6EB35; D6RBX0; D6RE01; D6RID9;
  • UniGene Hs.379754;
  • GeneID 340061
  • KEGG hsa:340061;
  • Human Stimulator of interferon genes protein Protein SEQUENCE
  • SEQUENCE 379 AA; 42193 MW; CB54D6A4D4D8E7C0 CRC64;

    MPHSSLHPSI PCPRGHGAQK AALVLLSACL VTLWGLGEPP EHTLRYLVLH

    LASLQLGLLL NGVCSLAEEL RHIHSRYRGS YWRTVRACLG CPLRRGALLL

    LSIYFYYSLP NAVGPPFTWM LALLGLSQAL NILLGLKGLA PAEISAVCEK

    GNFNVAHGLA WSYYIGYLRL ILPELQARIR TYNQHYNNLL RGAVSQRLYI

    LLPLDCGVPD NLSMADPNIR FLDKLPQQTG DHAGIKDRVY SNSIYELLEN

    GQRAGTCVLE YATPLQTLFA MSQYSQAGFS REDRLEQAKL FCRTLEDILA

    DAPESQNNCR LIAYQEPADD SSFSLSQEVL RHLRQEEKEE VTVGSLKTSA

    VPSTSTMSQE PELLISGMEK PLPLRTDFS

  • UCSC uc003lep.4; human.;



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