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Recombinant Rat CD44 Fc Chimera Protein, CF 50 UG

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Recombinant Rat CD44 Fc Chimera Protein, CF 50 UG信息二維碼

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產(chǎn)品介紹

    基本參數(shù)

    詳細說明

    • Purity

      >95%, by SDS-PAGE under reducing conditions and visualized by silver stain

    • Endotoxin Level

      <1.0 EU per 1 μg of the protein by the LAL method.  

    • Activity

      Measured by its binding ability in a functional ELISA.

      When Recombinant Rat CD44 Fc Chimera is present at 1 μg/mL, the concentration of biotinylated hyaluronan that produces 50% of the optimal binding response is found to be approximately 10-50 ng/mL.

    • Source

      Mouse myeloma cell line, NS0-derived

      Rat CD44
      (Gln22 - Glu271)
      Accession # O70509
      IEGRMDPMouse IgG2A
      (Glu98 - Lys330)
      N-terminus
      C-terminus
    • Accession #

    • N-terminal Sequence    
      Analysis

      Result not obtained, Gln22 is predicted

    • Structure / Form

      Disulfide-linked homodimer    
       

    • Predicted Molecular Mass

      54.2 kDa (monomer)

    • SDS-PAGE

      80-100 kDa, reducing conditions

    6577-CD

     

    Formulation Lyophilized from a 0.2 μm filtered solution in PBS.


    Reconstitution Reconstitute at 100 μg/mL in PBS.



    Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.


    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.

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


    Background: CD44

    CD44 is a ubiquitously expressed protein that is the major receptor for hyaluronan and exerts control over cell growth and migration (1 - 5). Rat CD44 has a 21 amino acid (aa) signal sequence, an extracellular domain (ECD) with a 100 aa hyaluronan?binding disulfide-stabilized link region and a 48 ? 463 aa stem region, a 21 aa transmembrane domain, and a 72 aa cytoplasmic domain. Within the stem, ten variably spliced exons (v1 - 10, exons 6 ? 15) produce multiple protein isoforms (1 - 5). The standard or hematopoietic form, CD44H, does not include the variable segments (1 - 5). Cancer aggressiveness and T cell activation have been correlated with expression of specific isoforms (2, 4). With variable N- and O-glycosylation and splicing within the stalk, CD44 can range from 80 to 200 kDa (1, 2). Within the ECD of CD44H, rat CD44 (aa 23 ? 271) shares 90%, 73%, 72%, 75% and 70% identity with corresponding mouse, human, equine, canine and bovine CD44, respectively. The many reported functions of CD44 fall within three categories (1, 2). First, CD44 binds hyaluronan and other ligands within the extracellular matrix and can function as a “platform” for growth factors and metalloproteinases. Second, CD44 is a co-receptor that modifies activity of receptors including MET and the ErbB family of tyrosine kinases. Third, the CD44 intracellular domain links the plasma membrane to the actin cytoskeleton via the ERM proteins, ezrin, radixin and moesin. CD44 can be synthesized in a soluble form (4) or may be cleaved at multiple sites by either membrane-type matrix metalloproteinases, or ADAM proteases to produce soluble ectodomains (6, 7). The cellular portion may then undergo gamma secretase-dependent intramembrane cleavage to form an A beta ?like transmembrane portion and a cytoplasmic signaling portion that affects gene expression (8, 9). These cleavage events are thought to promote metastasis by enhancing tumor cell motility and growth (1, 2, 6).

    • References:

      1. Pure, E. and R.K. Assoian (2009) Cell. Signal. 21:651.

      2. Ponta, H. et al. (2003) Nat. Rev. Mol. Cell Biol. 4:33.

      3. Screaton, G.R. et al. (1992) Proc. Natl. Acad. Sci. USA 89:12160.

      4. Lynch, K.W. (2004) Nat. Rev. Immunol. 4:931.

      5. Yu, Q. and B.P. Toole (1996) J. Biol. Chem. 271:20603.

      6. Nagano, O. and H. Saya (2004) Cancer Sci. 95:930.

      7. Nakamura, H. et al. (2004) Cancer Res. 64:876.

      8. Murakami, D. et al. (2003) Oncogene 22:1511.

      9. Lammich, S. et al. (2002) J. Biol. Chem. 277:44754.

    • Entrez Gene IDs:

      960 (Human); 12505 (Mouse); 25406 (Rat); 100126860 (Porcine)

    • Alternate Names:

      CD44 antigen; CD44 molecule (Indian blood group); CD44; CD44R; CDw44; cell surface glycoprotein CD44; chondroitin sulfate proteoglycan 8; CSPG8; ECMR-III; epican; Extracellular matrix receptor III; GP90 lymphocyte homing/adhesion receptor; HCAM; HCELL; hematopoietic cell E- and L-selectin ligand; Heparan sulfate proteoglycan; Hermes antigen; homing function and Indian blood group system; HUTCH-I; Hyaluronate receptor; IN; LHR; MC56; MDU2; MDU2CD44 antigen (homing function and Indian blood group system); MDU3; MDU3CDW44; MIC4; MIC4MGC10468; MUTCH-I; Pgp1; PGP-1; PGP-I; Phagocytic glycoprotein 1; Phagocytic glycoprotein I

























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