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Human ESAM Affinity Purified Polyclonal Ab 25 UG

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Human ESAM Affinity Purified Polyclonal Ab 25 UG信息二維碼

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Anti-NuMA antibody [EP3976]  10μl Anti-NuMA antibody [EP3976]  40μl Anti-NuMA antibody [EP3976]  100μl Anti-Nuf2 antibody [EPR13019]  10μl Anti-Nuf2 antibody [EPR13019]  40μl Anti-Nuf2 antibody [EPR13019]  100μl

產(chǎn)品介紹

    基本參數(shù)

    詳細(xì)說明

    • Species Reactivity

      Human

    • Specificity

      Detects human ESAM in direct ELISAs and Western blots. In direct ELISAs, approximately 5% cross?reactivity with recombinant mouse ESAM is observed.

    • Source

      Polyclonal Goat IgG

    • Purification

      Antigen Affinity-purified

    • Immunogen

      Mouse myeloma cell line NS0-derived recombinant human ESAM    
      Gln30-Ala247    
      Accession # Q96AP7

    • 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.

    • Label

      Unconjugated

    Applications

    • Recommended    
      Concentration

      Sample

    • Western Blot

      1 μg/mL

      See below


    • Flow Cytometry

      2.5 μg/10    6 cells

      See below


    • Immunohistochemistry

      5-15 μg/mL

      Immersion fixed paraffin-embedded sections of human kidney and liver


    • 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 ESAM by Western Blot. Western blot shows lysates of HUVEC human umbilical vein endothelial cells. PVDF membrane was probed with 1 μg/mL of Goat Anti-Human ESAM Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2688) followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # ). A specific band was detected for ESAM at approximately 55 kDa (as indicated). This experiment was conducted under reducing conditions and using .

    Flow Cytometry      
         

    Detection of ESAM in HUVEC Human Cells by Flow Cytometry. HUVEC human umbilical vein endothelial cells were stained with Goat Anti-Human ESAM Antigen Affinity?purified Polyclonal Antibody (Catalog # AF2688, filled histogram) or control antibody (Catalog # , open histogram), followed by Phycoerythrin-conjugated Anti-Goat 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: ESAM

    Endothelial cell-selective adhesion molecule (ESAM) is a 55 kDa type I transmembrane glycoprotein that belongs to the JAM family of immunoglobulin superfamily molecules (1, 2). Human ESAM is synthesized as a 390 amino acid (aa) protein composed of a 29 aa signal peptide, a 216 aa extracellular region, a putative 26 aa transmembrane segment, and a 119 aa cytoplasmic domain. The extracellular region contains one V-type and one C2-type Ig domain and is involved in homophilic adhesion (1). In the cytoplasmic domain, there is a docking site for the multifunctional adaptor protein MAGI-1 (3). The extracellular region of human ESAM shows 90%, 74%, 69% and 67% aa identity with monkey, canine, mouse and rat extracellular ESAM, respectively. ESAM is expressed on endothelial cells, activated platelets and megakaryocytes, and can be found associated with cell-to-cell junctions. Whether ESAM is restricted to a particular junctional type is not clear (1, 2). ESAM deficient mice have no defect in vascularization but do have reduced angiogenic potential. This may be due to a decreased migratory response to FGF-2 (4).

    • References:

      1. Hirata, K-I, et al. (2001) J. Biol. Chem. 276:16223.

      2. Nasdala, I. et al. (2002) J. Biol. Chem. 277:16294.

      3. Wegmann, F. et al. (2004) Exp. Cell Res. 300:121.

      4. Ishida, T. et. al. (2003) J. Biol. Chem. 278:34598.

    • Long Name:

      Endothelial Cell Adhesion Molecule

    • Entrez Gene IDs:

      90952 (Human); 69524 (Mouse)

    • Alternate Names:

      2310008D05Rik; endothelial cell adhesion molecule; endothelial cell-selective adhesion molecule; ESAM; HUEL (C4orf1)-interacting protein; LP4791 protein; W117m






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