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FLNB antibody

The Rabbit Polyclonal anti-FLNB antibody has been validated for IHC and IF. It is suitable to detect FLNB in samples from Human, Mouse and Rat.
Catalog No. ABIN7260435

Quick Overview for FLNB antibody (ABIN7260435)

Target

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

Reactivity

  • 54
  • 8
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

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

  • 51
  • 19
  • 16
  • 14
  • 13
  • 13
  • 10
  • 9
  • 8
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human FLNB (NP_001157789.1).

    Isotype

    IgG
  • Application Notes

    IHC 1:50-1:100 IF 1:20-1:100

    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

    FLNB (Filamin B, beta (FLNB))

    Alternative Name

    FLNB

    Background

    This gene encodes a member of the filamin family. The encoded protein interacts with glycoprotein Ib alpha as part of the process to repair vascular injuries. The platelet glycoprotein Ib complex includes glycoprotein Ib alpha, and it binds the actin cytoskeleton. Mutations in this gene have been found in several conditions: atelosteogenesis type 1 and type 3, boomerang dysplasia, autosomal dominant Larsen syndrome, and spondylocarpotarsal synostosis syndrome. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene.

    Gene ID

    2317

    UniProt

    O75369

    Pathways

    Maintenance of Protein Location
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