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Filamin A antibody

This Rabbit Monoclonal antibody specifically detects Filamin A in WB and IHC. It exhibits reactivity toward Human.
Catalog No. ABIN1682545
-15% Promotion 2026
$334.05
$393.00
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Quick Overview for Filamin A antibody (ABIN1682545)

Target

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

Reactivity

  • 116
  • 42
  • 31
  • 3
  • 2
  • 1
Human

Host

  • 107
  • 9
  • 1
Rabbit

Clonality

  • 85
  • 32
Monoclonal

Conjugate

  • 49
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  • 4
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  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
This Filamin A antibody is un-conjugated

Application

  • 65
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  • 17
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Western Blotting (WB), Immunohistochemistry (IHC)
  • Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthesized peptide derived from human Filamin A

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:50 - 1:200

    Restrictions

    For Research Use only
  • Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,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

    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.[provided by RefSeq, Mar 2009],ABP-280, ABPX, CSBS, CVD1, FLN, FLN-A, FLN1, FMD, MNS, NHBP, OPD, OPD1, OPD2, XLVD, XMVD,Cell Biology & Developmental Biology,Cytoskeleton,Cytoskeleton_Actins,Cytoskeleton_Microfilaments,Epigenetics & Nuclear Signaling,MAPK-Erk Signaling Pathway,Protein phosphorylation,RNA Binding,Signal Transduction,FLNA

    Molecular Weight

    281 kDa

    Gene ID

    2316

    UniProt

    P21333

    Pathways

    TCR Signaling, Maintenance of Protein Location
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