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FLNB antibody (AA 30-239)

This Rabbit Polyclonal antibody specifically detects FLNB in WB and IF. It exhibits reactivity toward Human.
Catalog No. ABIN1886344

Quick Overview for FLNB antibody (AA 30-239) (ABIN1886344)

Target

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

Reactivity

  • 54
  • 9
  • 5
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human

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
  • 14
  • 13
  • 13
  • 10
  • 9
  • 8
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Binding Specificity

    • 15
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 30-239

    Purification

    Affinity purified by Protein A.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 30 and 239 of Filamin B
  • Application Notes

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunofluorescence: 1.100-1.200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    1 x PBS, 1 % BSA, 20 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target

    FLNB (Filamin B, beta (FLNB))

    Alternative Name

    Filamin B

    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.[provided by RefSeq]

    Molecular Weight

    278 kDa

    Gene ID

    2317

    NCBI Accession

    NP_001448, NM_001457

    Pathways

    Maintenance of Protein Location
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