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Filamin A antibody

FLNA Reactivity: Human, Mouse, Rat IHC, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7259092
  • Target See all Filamin A (FLNA) Antibodies
    Filamin A (FLNA) (Filamin A, alpha (FLNA))
    Reactivity
    • 101
    • 32
    • 27
    • 3
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 94
    • 6
    • 1
    Rabbit
    Clonality
    • 85
    • 16
    Polyclonal
    Conjugate
    • 42
    • 7
    • 5
    • 5
    • 5
    • 5
    • 5
    • 5
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    This Filamin A antibody is un-conjugated
    Application
    • 51
    • 31
    • 28
    • 28
    • 26
    • 23
    • 11
    • 9
    • 7
    • 6
    • 4
    • 3
    • 2
    • 2
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    A synthetic peptide of human FLNA (NP_001104026.1).
    Isotype
    IgG
    Top Product
    Discover our top product FLNA Primary Antibody
  • Application Notes
    IHC 1:50-1:200 IF 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Filamin A (FLNA) (Filamin A, alpha (FLNA))
    Alternative Name
    FLNA (FLNA Products)
    Background
    The protein encoded by this gene is an actin-binding protein that crosslinks actin filaments and links actin filaments to membrane glycoproteins. The encoded protein is involved in remodeling the cytoskeleton to effect changes in cell shape and migration. This protein interacts with integrins, transmembrane receptor complexes, and second messengers. Defects in this gene are a cause of several syndromes, including periventricular nodular heterotopias (PVNH1, PVNH4), otopalatodigital syndromes (OPD1, OPD2), frontometaphyseal dysplasia (FMD), Melnick-Needles syndrome (MNS), and X-linked congenital idiopathic intestinal pseudoobstruction (CIIPX). Two transcript variants encoding different isoforms have been found for this gene.
    Gene ID
    2316
    UniProt
    P21333
    Pathways
    TCR Signaling, Maintenance of Protein Location
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