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Fukutin anticorps (AA 222-456)

Cet anticorps anti-Fukutin est un anticorps Lapin Polyclonal détectant Fukutin dans WB et IF. Adapté pour Humain.
N° du produit ABIN1886220

Aperçu rapide pour Fukutin anticorps (AA 222-456) (ABIN1886220)

Antigène

Voir toutes Fukutin (FKTN) Anticorps
Fukutin (FKTN)

Reactivité

  • 38
  • 24
  • 9
  • 6
  • 5
  • 4
  • 4
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
Humain

Hôte

  • 38
  • 1
Lapin

Clonalité

  • 36
  • 3
Polyclonal

Conjugué

  • 24
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Fukutin est non-conjugé

Application

  • 29
  • 17
  • 15
  • 6
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Épitope

    • 8
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 222-456

    Purification

    Purified by antigen-affinity chromatography.

    Immunogène

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 222 and 456 of Human FKTN
  • Indications d'application

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

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % 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

    Fukutin (FKTN)

    Autre désignation

    fukutin

    Sujet

    The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle.The encoded protein is thought to be a glycosyltransferase and could play a role in brain development.Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X).Two transcript variants encoding the same protein have been found for this gene.[provided by RefSeq]

    Poids moléculaire

    54 kDa

    ID gène

    2218

    NCBI Accession

    NM_006731, NP_006722

    Pathways

    Regulation of Carbohydrate Metabolic Process
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