G-CSFR Polyclonal Antibody

    • Catalog No.:YT5527
    • Applications:WB;ELISA
    • Reactivity:Human;Rat;Mouse;
      • Target:
      • G-CSFR
      • Fields:
      • >>Cytokine-cytokine receptor interaction;>>PI3K-Akt signaling pathway;>>JAK-STAT signaling pathway;>>Hematopoietic cell lineage;>>Pathways in cancer
      • Gene Name:
      • CSF3R
      • Protein Name:
      • Granulocyte colony-stimulating factor receptor
      • Human Gene Id:
      • 1441
      • Human Swiss Prot No:
      • Q99062
      • Mouse Swiss Prot No:
      • P40223
      • Immunogen:
      • The antiserum was produced against synthesized peptide derived from the Internal region of human CSF3R. AA range:321-370
      • Specificity:
      • G-CSFR Polyclonal Antibody detects endogenous levels of G-CSFR protein.
      • Formulation:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • Source:
      • Polyclonal, Rabbit,IgG
      • Dilution:
      • WB 1:500 - 1:2000. ELISA: 1:20000. Not yet tested in other applications.
      • Purification:
      • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
      • Concentration:
      • 1 mg/ml
      • Storage Stability:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • Other Name:
      • CSF3R;GCSFR;Granulocyte colony-stimulating factor receptor;G-CSF receptor;G-CSF-R;CD114
      • Observed Band(KD):
      • 92kD
      • Background:
      • The protein encoded by this gene is the receptor for colony stimulating factor 3, a cytokine that controls the production, differentiation, and function of granulocytes. The encoded protein, which is a member of the family of cytokine receptors, may also function in some cell surface adhesion or recognition processes. Alternatively spliced transcript variants have been described. Mutations in this gene are a cause of Kostmann syndrome, also known as severe congenital neutropenia. [provided by RefSeq, Aug 2010],
      • Function:
      • alternative products:Additional isoforms seem to exist. Experimental confirmation may be lacking for some isoforms,disease:Defects in CSF3R may be a cause of severe congenital neutropenia (SCN) in some patients.,domain:The box 1 motif is required for JAK interaction and/or activation.,domain:The WSXWS motif appears to be necessary for proper protein folding and thereby efficient intracellular transport and cell-surface receptor binding.,function:Receptor for granulocyte colony-stimulating factor (CSF3). In addition it may function in some adhesion or recognition events at the cell surface.,similarity:Belongs to the type I cytokine receptor family. Type 2 subfamily.,similarity:Contains 1 Ig-like C2-type (immunoglobulin-like) domain.,similarity:Contains 5 fibronectin type-III domains.,subunit:Homodimer. The dimeric receptor binds two CSF3 molecules.,tissue specificity:One or several isofor
      • Subcellular Location:
      • [Isoform 2]: Secreted .; Cell membrane ; Single-pass type I membrane protein .
      • Expression:
      • One or several isoforms have been found in myelogenous leukemia cell line KG-1, leukemia U-937 cell line, in bone marrow cells, placenta, and peripheral blood granulocytes. Isoform GCSFR-2 is found only in leukemia U-937 cells. Isoform GCSFR-3 is highly expressed in placenta.
      • Products Images
      • Western Blot analysis of SKOV3 cells using G-CSFR Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000