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Human CD2 ELISA Kit

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  • Alternative name

    Human erythrocyte receptor ELISA Kit;Human LFA-2 ELISA Kit;Human LFA-3 receptor ELISA Kit;Human rosette receptor ELISA Kit;Human T-cell surface antigen T11/Leu-5 ELISA Kit;Human SRBC ELISA Kit;Human T11 ELISA Kit;Human CD2 molecule ELISA Kit;Human T-cell surface antigen CD2 ELISA Kit;Human CD2 antigen (p50), sheep red blood cell receptor ELISA Kit;Human lymphocyte-function antigen-2 ELISA Kit;
  • Catalog
    E010652
  • species
    Human
  • GeneCD2
  • Standard CurveHuman CD2 ELISA Kit
  • Other Species Human LFA-2/CD2 ELISA KitMouse Cd2 ELISA KitHorse CD2 ELISA KitMonkey CD2 ELISA KitRat Cd2 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of CCND2. No significant cross-reactivity or interference between CCND2 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between CCND2 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 CD2 ELISA Kit allows for the in vitro quantitative determination of CD2 , concentrations in serum, Plasma , tissue homogenates and Cell culture supernates and Other biological fluids.
  • StorageStore the whole ELISA kit at 4℃
  • Product Categories/FamilyHuman ELISA Kit
  • Product Description
    specifical    Intended Uses: This CCND2 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human CCND2. This ELISA kit for research use only, not for therapeutic or diagnostic applications! Principle of the Assay: CCND2 ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for CCND2. Standards or samples are then added to the microtiter plate wells and CCND2 if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of CCND2 present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for CCND2 are added to each well to "sandwich" the CCND2 immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. Next, substrate solutions are added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period. Only those wells that contain CCND2 and enzyme-conjugated antibody will exhibit a change in color. The enzyme-substrate reaction is terminated by addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The CCND2 concentration in each sample is interpolated from this standard curve.
  • Human T-cell surface antigen CD2 Protein information
  • Uniprot ID CD2_HUMAN
  • Uniprot AC P06729; Q96TE5;
  • UniGene Hs.523500;
  • GeneID 914
  • KEGG hsa:914;
  • Human T-cell surface antigen CD2 Protein SEQUENCE

  • SEQUENCE 351 AA; 39448 MW; A03D853C3B618917 CRC64;

    MSFPCKFVAS FLLIFNVSSK GAVSKEITNA LETWGALGQD INLDIPSFQM

    SDDIDDIKWE KTSDKKKIAQ FRKEKETFKE KDTYKLFKNG TLKIKHLKTD

    DQDIYKVSIY DTKGKNVLEK IFDLKIQERV SKPKISWTCI NTTLTCEVMN

    GTDPELNLYQ DGKHLKLSQR VITHKWTTSL SAKFKCTAGN KVSKESSVEP

    VSCPEKGLDI YLIIGICGGG SLLMVFVALL VFYITKRKKQ RSRRNDEELE

    TRAHRVATEE RGRKPHQIPA STPQNPATSQ HPPPPPGHRS QAPSHRPPPP

    GHRVQHQPQK RPPAPSGTQV HQQKGPPLPR PRVQPKPPHG AAENSLSPSS

    N



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