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FLNB anticorps (AA 30-239)

Cet anticorps Lapin Polyclonal détecte spécifiquement FLNB dans WB et IF. Il présente une réactivité envers Humain.
N° du produit ABIN1886344

Aperçu rapide pour FLNB anticorps (AA 30-239) (ABIN1886344)

Antigène

Voir toutes FLNB Anticorps
FLNB (Filamin B, beta (FLNB))

Reactivité

  • 49
  • 9
  • 5
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 42
  • 6
  • 1
Lapin

Clonalité

  • 43
  • 6
Polyclonal

Conjugué

  • 31
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp FLNB est non-conjugé

Application

  • 45
  • 15
  • 13
  • 13
  • 13
  • 12
  • 10
  • 9
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Épitope

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

    Purification

    Affinity purified by Protein A.

    Immunogène

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 30 and 239 of Filamin B
  • Indications d'application

    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.

    Agent conservateur

    Thimerosal (Merthiolate)

    Précaution d'utilisation

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Stock

    4 °C/-20 °C

    Stockage commentaire

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

    FLNB (Filamin B, beta (FLNB))

    Autre désignation

    Filamin B

    Sujet

    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]

    Poids moléculaire

    278 kDa

    ID gène

    2317

    NCBI Accession

    NP_001448, NM_001457

    Pathways

    Maintenance of Protein Location
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