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FLNB antibody (AA 2552-2602)

The Rabbit Polyclonal anti-FLNB antibody has been validated for WB and IHC (fp). It is suitable to detect FLNB in samples from Human and Mouse.
Catalog No. ABIN7454539

Quick Overview for FLNB antibody (AA 2552-2602) (ABIN7454539)

Target

See all FLNB Antibodies
FLNB (Filamin B, beta (FLNB))

Reactivity

  • 54
  • 8
  • 5
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 47
  • 6
  • 1
Rabbit

Clonality

  • 48
  • 6
Polyclonal

Conjugate

  • 36
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This FLNB antibody is un-conjugated

Application

  • 50
  • 20
  • 16
  • 15
  • 13
  • 13
  • 10
  • 9
  • 8
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Formalin-fixed Paraffin-embedded Sections) (IHC (fp))
  • Binding Specificity

    • 15
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 2552-2602

    Purpose

    Rabbit anti-Filamin B Antibody, Affinity Purified

    Predicted Reactivity

    Rabbit

    Purification

    Affinity Purified

    Immunogen

    between AA 2552 and 2602

    Isotype

    IgG
  • Application Notes

    IHC: 1:200 - 1:1,000. Epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.

    IP: Not recommended

    WB: 1:2,000 - 1:10,000

    Restrictions

    For Research Use only
  • Concentration

    200 μg/mL

    Buffer

    Tris-buffered Saline containing 0.1 % BSA and 0.09 % Sodium Azide

    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

    Expiry Date

    12 months
  • Target

    FLNB (Filamin B, beta (FLNB))

    Alternative Name

    Filamin B

    Background

    Background: Filamin B is a cytoplasmic protein that functions to link cell membrane proteins to the actin cytoskeleton. Defects in Filamin B are associated with a number of diseases characterized by skeletal dysplasias and abnormalities.

    Gene ID

    2317

    NCBI Accession

    NP_001448

    UniProt

    O75369

    Pathways

    Maintenance of Protein Location
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