Human DARS ELISA Kit

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  • Alternative name

    Human aspartyl-tRNA synthetase ELISA Kit;Human aspRS ELISA Kit;Human cell proliferation-inducing gene 40 protein ELISA Kit;Human HBSL ELISA Kit;Human aspartate--tRNA ligase, cytoplasmic ELISA Kit;Human aspartate tRNA ligase 1, cytoplasmic ELISA Kit;Human aspartyl-tRNA synthetase, cytoplasmic ELISA Kit;Human testicular tissue protein Li 192 ELISA Kit;

  • Catalog
    E003849
  • species
    Human
  • GeneDARS
  • Standard CurveHuman DARS ELISA Kit
  • Other Species Mouse Dars ELISA KitBovine DARS ELISA KitRat Dars ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of DARS. No significant cross-reactivity or interference between DARS and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between DARS and all the analogues, therefore, cross reaction may still exist in some cases.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity1.0 ng/mL.
  • Intended UseHuman DARS ELISA Kit allows for the in vitro quantitative determination of DARS , concentrations in serum, Plasma , tissue homogenates and Cell culture supernates and Other biological fluids.
  • StorageStore the whole ELISA kit at 4℃
  • Product Categories/FamilyEpigenetics and Nuclear Signaling
  • Product Description
    specifical
    Intended Uses: This DARS ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human DARS. This ELISA kit for research use only, not for therapeutic or diagnostic applications! Principle of the Assay: DARS ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-DARS antibody and an DARS-HRP conjugate. The assay sample and buffer are incubated together with DARS-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 DARS concentration since DARS from samples and DARS-HRP conjugate compete for the anti-DARS antibody binding site. Since the number of sites is limited, as more sites are occupied by DARS from the sample, fewer sites are left to bind DARS-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The DARS concentration in each sample is interpolated from this standard curve.
  • Human Aspartate--tRNA ligase, cytoplasmic Protein information
  • Uniprot ID SYDC_HUMAN
  • Uniprot AC Q9BW52;
  • UniGene Hs.503787; Hs.595819;
  • GeneID 1615
  • KEGG hsa:1615;
  • Human Aspartate--tRNA ligase, cytoplasmic Protein SEQUENCE
  • SEQUENCE 501 AA; 57136 MW; B181572DF0AF5F94 CRC64;

    MPSASASRKS QEKPREIMDA AEDYAKERYG ISSMIQSQEK PDRVLVRVRD

    LTIQKADEVV WVRARVHTSR AKGKQCFLVL RQQQFNVQAL VAVGDHASKQ

    MVKFAANINK ESIVDVEGVV RKVNQKIGSC TQQDVELHVQ KIYVISLAEP

    RLPLQLDDAV RPEAEGEEEG RATVNQDTRL DNRVIDLRTS TSQAVFRLQS

    GICHLFRETL INKGFVEIQT PKIISAASEG GANVFTVSYF KNNAYLAQSP

    QLYKQMCICA DFEKVFSIGP VFRAEDSNTH RHLTEFVGLD IEMAFNYHYH

    EVMEEIADTM VQIFKGLQER FQTEIQTVNK QFPCEPFKFL EPTLRLEYCE

    ALAMLREAGV EMGDEDDLST PNEKLLGHLV KEKYDTDFYI LDKYPLAVRP

    FYTMPDPRNP KQSNSYDMFM RGEEILSGAQ RIHDPQLLTE RALHHGIDLE

    KIKAYIDSFR FGAPPHAGGG IGLERVTMLF LGLHNVRQTS MFPRDPKRLT

    P

  • UCSC uc002tux.2; human. [P14868-1];


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