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Filamin A antibody (pSer2152)

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Catalog No. ABIN7250800

Quick Overview for Filamin A antibody (pSer2152) (ABIN7250800)

Target

See all Filamin A (FLNA) Antibodies
Filamin A (FLNA) (Filamin A, alpha (FLNA))

Reactivity

  • 108
  • 33
  • 22
  • 2
  • 2
  • 1
Human, Mouse, Rat, Monkey

Host

  • 99
  • 9
  • 1
Rabbit

Clonality

  • 87
  • 22
Polyclonal

Conjugate

  • 50
  • 7
  • 5
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
This Filamin A antibody is un-conjugated

Application

  • 57
  • 34
  • 34
  • 28
  • 28
  • 23
  • 16
  • 13
  • 10
  • 7
  • 6
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Binding Specificity

    • 15
    • 15
    • 12
    • 6
    • 5
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    pSer2152

    Characteristics

    Phosphorylated antibody

    Purification

    Affinity purification

    Immunogen

    Synthesized peptide derived from human Filamin 1 around the phosphorylation site of Ser2152

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000, IHC 1:100-1:300, ELISA 1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 0.5 % BSA and 50 % glycerol, pH 7.4

    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

    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.

    Molecular Weight

    Observed_MW: 280 kDa

    Calculated_MW: 281 kDa

    UniProt

    P21333

    Pathways

    TCR Signaling, Maintenance of Protein Location
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