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Recombinant Human MAdCAM-1 Fc Chimera Protein, CF 50 UG

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Recombinant Human MAdCAM-1 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(xì)說明

    • Purity

      >95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie? Blue Staining.

    • Endotoxin Level

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

    • Activity

      Measured by the ability of the immobilized protein to support the adhesion of HuT 78 human cutaneous T cell lymphoma cells. When 5 x 10    4 cells/well are added to recombinant human MAdCAM-1/Fc Chimera coated plates (2.5 μg/mL with 100 μL/well), approximately 50%-70% will adhere after 1 hour incubation at 37 °C in the presence of 1 mM MnCl    2.    
         Optimal dilutions should be determined by each laboratory for each application.  

    • Source

      Mouse myeloma cell line, NS0-derived

      Human MAdCAM-1
      Met1-Gln333
      Accession # AAY82472
      IEGRMDHuman IgG1
      (Pro100-Lys333)
      N-terminus
      C-terminus
    • Accession #

    • N-terminal Sequence    
      Analysis

      Val23 & Glu29    
       

    • Structure / Form

      Disulfide-linked homodimer    
       

    • Predicted Molecular Mass

      59.3 kDa (monomer)

    • SDS-PAGE

      85-100 kDa, reducing conditions

    6056-MC

     

    Formulation Lyophilized from a 0.2 μm filtered solution in PBS.


    Reconstitution Reconstitute at 200 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: MAdCAM-1

    Mucosal addressin cell adhesion molecule-1 (MAdCAM-1) is an approximately 60 kDa type 1 transmembrane glycoprotein. It is an endothelial cell adhesion molecule that belongs to the immunoglobulin (Ig) superfamily of proteins (1). Human MAdCAM-1 is synthesized as a 382 amino acid (aa) precursor that contains an 18 aa signal sequence, a 299 aa extracellular domain (ECD), a 21 aa transmembrane segment, and a 44 aa cytoplasmic tail. Within the ECD there is one potential site for N-linked glycosylation (2). The ECD comprises two Ig-like domains of 90 aa and 119 aa, respectively, each possessing invariant cysteine residues that stabilize the Ig loop (2). There is also a Ser-Thr-Pro-rich (71%) mucin-like 48 aa domain that is (aa 206 ? 317) formed by six tandem repeats of an eight aa sequence having the general consensus DTTSPEP/SP. This mucin domain contains 19 potential sites for O-linked glycosylation (2, 3). A splicing variant in which a single Ala residue is substituted for aa 223 ? 334 in isoform 1 produces a second isoform. Human mature MAdCAM-1 shares only 44% aa sequence identity with mature mouse MAdCAM-1. The integrin alpha (4)  beta (7), which is expressed on lymphocytes, functions as the MAdCAM-1 receptor (1). The Ig domains of MAdCAM-1 are critical to alpha (4)  beta (7)  binding, and the mucin domain has activity in L?Selectin binding. MAdCAM-1 expression is up-regulated by TNF-alpha  and IL?1 beta. MAdCAM-1 is expressed on the surface of high endothelial venules (HEV) in the gut and in Peyer’s patches, on endothelial cells of the mesenteric lymph nodes, lamina propria of the small and large intestine, and the mammary gland during lactation, and on brain endothelial cells (1). MAdCAM?1 has also been reported to be expressed in the liver portal region in autoimmune hepatitis (1), and in bone marrow following allogenic (genetically non-identical) hematopoietic stem cell transplantation, where it recruits donor T cells, which may lead to graft versus host disease (3, 4). MAdCAM?1 functions as a homing receptor, and plays a central role in leukocyte migration into HEVs and Peyer’s patch (5). In addition to its normal role in lymphocyte trafficking to mucosal tissue, MAdCAM?1 expression is also dramatically increased in chronic inflammatory and disease states (1, 6), including inflammatory bowel disease (Crohn’s disease and ulcerative colitis) (7), sclerosing cholangitis (8), and diabetes (9), and may play an important role in these conditions.

    • References:

      1. Ando, T. et al. (2007) BMC Physiol. 7:10.

      2. Dando, J. et al. (2002) Acta Crystallogr. D 58:233.

      3. Leung, E. et al. (1996) Immunol. Cell Biol. 74:490.

      4. Ambruzova, Z. et al. (2009) Hum. Immunol. 70:457.

      5. Tada, T. et al. (2008) Exp. Anim. 57:247.

      6. Volpes, R. et al. (1992) Hepatology 15:269.

      7. Connor, E.M. et al. (1999) J. Leukoc. Biol. 65:349.

      8. Ala, A. et al. (2001) Gut 49:3043.

      9. Yang, X.D. et al. (1997) Diabetes 46:1542.

    • Long Name:

      Mucosal Addressin Cell Adhesion Molecule 1

    • Entrez Gene IDs:

      8174 (Human); 17123 (Mouse)

    • Alternate Names:

      hMAdCAM-1; MACAM1; MAdCAM1; MAdCAM-1; mucosal addressin cell adhesion molecule 1; mucosal addressin cell adhesion molecule-1; mucosal vascular addressin cell adhesion molecule 1




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