Human GPR56 Affinity Purified Polyclonal Ab 25 UG

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Human GPR56 Affinity Purified Polyclonal Ab 25 UG信息二维码

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产品介绍

    基本参数

    详细说明

    • Species Reactivity

      Human

    • Specificity

      Detects human GPR56 in direct ELISAs and Western blots. In direct ELISAs, less than 1% cross-reactivity with recombinant human (rh) GPR30, rhGPR114, rhGPR115, rhGPR124, and rhGPR125 is observed.

    • Source

      Polyclonal Sheep IgG

    • Purification

      Antigen Affinity-purified

    • Immunogen

      Chinese hamster ovary cell line CHO-derived recombinant human GPR56    
      Arg26-Val342    
      Accession # AAP35975

    • Formulation

      Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied as a 0.2 µm filtered solution in PBS.

    • Endotoxin Level

      <0.10 EU per 1 μg of the antibody by the LAL method.  

    • Label

      Unconjugated

    Applications

    • Recommended    
      Concentration

      Sample

    • Western Blot

      1 µg/mL

      See below


    • Flow Cytometry

      2.5 µg/10    6 cells

      See below


    • CyTOF-ready

      Ready to be labeled using established conjugation methods. No BSA or other carrier proteins that could interfere with conjugation.


    Please Note: Optimal dilutions should be determined by each laboratory for each application.  are available in the Technical Information section on our website.

    Data Examples

    Western Blot      
         

    Detection of Human GPR56 by Western Blot. Western blot shows lysates of human brain (cortex) tissue and human brain (hippocampus) tissue. PVDF membrane was probed with 1 µg/mL of Sheep Anti-Human GPR56 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF4634) followed by HRP-conjugated Anti-Sheep IgG Secondary Antibody (Catalog # ). A specific band was detected for GPR56 at approximately 65 kDa (as indicated). This experiment was conducted under reducing conditions and using .

    Flow Cytometry      
         

    Detection of GPR56 in Human Blood Lymphocytes by Flow Cytometry.

    Human peripheral blood lymphocytes were stained with Sheep Anti-Human GPR56 Affinity-purified Polyclonal Antibody (Catalog # AF4634, filled histogram) or control antibody (Catalog # , open histogram), followed by Phycoerythrin-conjugated Anti-Sheep IgG Secondary Antibody (Catalog # ).

    Preparation and Storage

    • Reconstitution

      Reconstitute at 0.2 mg/mL in sterile PBS.

    • Shipping

      The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. *Small pack size (SP) is shipped with polar packs. Upon receipt, store it immediately at -20 to -70 °C

    • Stability & Storage

      Use a manual defrost freezer and avoid repeated freeze-thaw cycles.    

      • 12 months from date of receipt, -20 to -70 °C as supplied.

      • 1 month, 2 to 8 °C under sterile conditions after reconstitution.

      • 6 months, -20 to -70 °C under sterile conditions after reconstitution.

    Background: GPR56

    GPR56 is a member of the LN-TM7 family of adhesion-type 7-transmembrane (TM) G-protein coupled receptors (GPCR) with long extracellular N-termini (1‑3). The 693 amino acid (aa) human GPR56 contains a 25 aa signal sequence, a 377 aa N-terminal extracellular domain (ECD) and seven TM regions separated by short intracellular and extracellular regions. Like other LN-TM7 members, the ECD contains a highly glycosylated mucin-like stalk followed by a GPCR proteolytic cleavage site (GPS) (1, 4). Cleavage of the 60 kDa N-terminus from the 80 kDa full length form is needed for efficient cell surface expression (5, 6). While the cleaved portion may remain non-covalently associated, it has also been found in conditioned medium of cultured cells (5). Human GPR56 shares 71%, 72%, 80%, 80% and 79% aa identity with mouse, rat, canine, equine, and bovine GPR56 within the cleaved ECD. A functional splice variant lacking the GPS site and a non-functional splice variant lacking portions of the TM domains have also been described (4). A human brain developmental disorder, bilateral frontoparietal polymicrogyria, is associated with GPR56 mutations that also show impaired GPS cleavage, intracellular trafficking, and expression at the cell surface (5). GPR56 is widely distributed, with highest mRNA or expressed sequence tag expression in brain, thyroid, skin and female reproductive system (3, 4). GPR56 expression is upregulated during cell transformation and is high in melanomas, glioblastomas and astrocytomas, but downregulated in melanomas with high metastatic potential (2, 6‑8). Although the function of GPR56 is not completely known, it is clearly an adhesion protein (6‑8). Tissue transglutaminase (TG2) is one reported ligand, binding of which inhibits melanoma growth and metastasis (6). Association of GPR56 with the tetraspanin CD81 stabilizes its complex with Gaq/11 for cell signaling (9).

    • References:

      1. Fredriksson, R. et al. (2002) FEBS Lett. 531:407.

      2. Zendman, A.J.W. et al. (1999) FEBS Lett. 446:292.

      3. Liu, M. et al. (1999) Genomics 55:296.

      4. Bjarnadottir, T.K. et al. (2007) Gene 387:38.

      5. Jin, Z. et al. (2007) Hum. Mol. Genet. 16:1972.

      6. Xu, L. et al. (2006) Proc. Natl. Acad. Sci. USA 103:9023.

      7. Shashidhar, S. et al. (2005) Oncogene 24:1673.

      8. Ke, N. et al. (2007) Mol. Cancer Ther. 6:1840.

      9. Little, K.D. et al. (2004) Mol. Biol. Cell 15:2375.

    • Long Name:

      G Protein-coupled Receptor 56

    • Entrez Gene IDs:

      9289 (Human); 14766 (Mouse); 260326 (Rat)

    • Alternate Names:

      BFPP; EGF-TM7-like; G protein-coupled receptor 56,7-transmembrane protein with no EGF-like N-terminal domains-1; GPR56; Protein TM7XN1; TM7LN4; TM7LN4G-protein coupled receptor 56; TM7XN1; TM7XN1DKFZp781L1398


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