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ITGA7 antibody (FITC)

ITGA7 Reactivity: Mouse FACS Host: Mouse Monoclonal 3C12 FITC
Catalog No. ABIN2853581
  • Target See all ITGA7 Antibodies
    ITGA7 (Integrin, alpha 7 (ITGA7))
    Reactivity
    • 46
    • 19
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Mouse
    Host
    • 42
    • 8
    • 1
    Mouse
    Clonality
    • 43
    • 8
    Monoclonal
    Conjugate
    • 28
    • 4
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This ITGA7 antibody is conjugated to FITC
    Application
    • 33
    • 21
    • 7
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Flow Cytometry (FACS)
    Cross-Reactivity (Details)
    Species reactivity (tested):Mouse.
    Purification
    Protein-A Sepharose Chromatography.
    Immunogen
    Mouse myoblasts. Remarks: Hybridoma was established by fusion of mouse myeloma cell SP2/0 with Integrinalpha-7 knockout C57/B6 Mouse splenocyte.
    Clone
    3C12
    Isotype
    IgG1
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    Discover our top product ITGA7 Primary Antibody
  • Application Notes
    Flow Cytometry: 25-50 μg/mL (final concentration). Positive Control: C2C12. Detailed Procedure is provided in the following Protocols.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.
    Protocol
    Flow Cytometric Analysis for Floating CellsWe usually use Fisher tubes or equivalents as reaction tubes for all step described below. 1) Wash the cells 3 times with washing buffer [PBS containing 2% fetal calf serum (FCS) and0. 1% NaN3]. 2) Resuspend the cells with washing buffer (5x10e6 cells/mL). 3) Add 50 µL of the cell suspension into each tube, and centrifuge at 500 x g for 1 minute atroom temperature (20~25°C). Remove supernatant by careful aspiration. 4) Add 10 µL of normal goat serum containing 1 mg/mL normal human IgG and 0. 1% NaN3to the cell pellet after tapping. Mix well and incubate for 5 minutes at room temperature. 5) Add 40 µL of the primary antibody at the concentration suggested in the APPLICATIONS,diluted in the washing buffer. Mix well and incubate for 30 minutes at room temperature. 6) Add 1 mL of the washing buffer followed by centrifugation at 500 x g for 1 minute at roomtemperature. Remove supernatant by careful aspiration. 7) Resuspend the cells with 500 µL of the washing buffer and analyze by a flow cytometer. Positive Control for Flow Cytometry: C2C12
    Restrictions
    For Research Use only
  • Concentration
    0.5 mg/mL
    Buffer
    PBS containing 1 % BSA as stabilizer and 0.09 % Sodium Azide as preservative.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    4 °C
    Storage Comment
    Store the antibody undiluted at 2-8 °C.
    Shelf life: one year from despatch.
    Expiry Date
    12 months
  • Target
    ITGA7 (Integrin, alpha 7 (ITGA7))
    Alternative Name
    Integrin alpha-7 / ITGA7 (ITGA7 Products)
    Synonyms
    [a]7 antibody, alpha7 antibody, integrin alpha 7 antibody, integrin subunit alpha 7 antibody, Itga7 antibody, ITGA7 antibody
    Background
    The integrin family of adhesion molecules participate in important cell-cell and cell-extracellular matrix interactions in a diverse range of biological processes. Integrins are heterodimers consisting of an alpha subunit and a beta subunit. Both alpha and beta subunits are transmembrane proteins with large extracellular domains (>100 kDa for alpha subunit and >75 kDa for beta subunit) that interact with extracellular matrix proteins and relatively small cytoplasmic domains (50 amino acids or less, except for the beta-4 subunit) that interact with cytoskeletal proteins. The adhesiveness of integrins is dynamically regulated in response to cytoplasmic signals, termed
    UniProt
    Q61738
    Pathways
    Integrin Complex
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