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IL-7R Polyclonal Antibody
Datasheet   

  • Catalog Number:

    E20-72341
  • Amount:

    100ul
  • Molecular Weight:

    51567Da
  • Applications:

    WB;IHC-p;IF(paraffin section);ELISA
  • Reactivity:

    Human;Mouse
  • Purification:

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • Immunogen:

    The antiserum was produced against synthesized peptide derived from human IL-7R/CD127. AA range:410-459
  • Source:

    Polyclonal, Rabbit,IgG
  • Western Blot analysis of various cells using IL-7R Polyclonal Antibody
  • Gene Name:

    IL7R
  • Dilution:

    Western Blot: 1/500 - 1/2000. ELISA: 1/40000. Not yet tested in other applications.
  • Protein Name:

    Interleukin-7 receptor subunit alpha
  • Human Gene Id:

    3575
  • Human Swiss Prot No:

    P16871
  • Mouse Gene Id:

    16197
  • Mouse Swiss Prot No:

    P16872
  • Specificity:

    IL-7R Polyclonal Antibody detects endogenous levels of IL-7R protein.
  • Formulation:

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • Concentration:

    1 mg/ml
  • Storage Stability:

    -20°C/1 year
  • Other Name:

    IL7R; Interleukin-7 receptor subunit alpha; IL-7 receptor subunit alpha; IL-7R subunit alpha; IL-7R-alpha; IL-7RA; CDw127; CD antigen CD127
  • Observed Band(KD):

    52 60
  • Background:

    The protein encoded by this gene is a receptor for interleukin 7 (IL7). The function of this receptor requires the interleukin 2 receptor, gamma chain (IL2RG), which is a common gamma chain shared by the receptors of various cytokines, including interleukins 2, 4, 7, 9, and 15. This protein has been shown to play a critical role in V(D)J recombination during lymphocyte development. Defects in this gene may be associated with severe combined immunodeficiency (SCID). Alternatively spliced transcript variants have been found. [provided by RefSeq, Dec 2015],
  • Function:

    disease:A genetic variation in transmembrane domain of IL7R is associated with susceptibility to multiple sclerosis (MS) [MIM:126200]. Overtransmission of the major 'C' allele coding for Thr-244 are detected in offspring affected with multiple sclerosis. In vitro analysis of transcripts from minigenes containing either 'C' allele (Thr-244) or 'T' allele (Ile-244) shows that the 'C' allele results in an approximately two-fold increase in the skipping of exon 6, leading to increased production of a soluble form of IL7R. Thus, the multiple sclerosis associated 'C' risk allele of IL7R would probably decrease membrane-bound expression of IL7R. As this risk allele is common in the general population, some additional triggers are probably required for the development and progression of MS.,disease:Defects in IL7R are a cause of autosomal recessive severe combined immunodeficiency T-cell-negativ
  • Subcellular Location:

    [Isoform 1]: Cell membrane; Single-pass type I membrane protein.; [Isoform 3]: Cell membrane; Single-pass type I membrane protein.; [Isoform 4]: Secreted.
  • Expression:

    B-cell,Epithelium,Spleen,Testis,Products Images
  • Western Blot analysis of K562 cells using IL-7R Polyclonal Antibody

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Catalog Number

  • Amount:100ul
  • Price:225$

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