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FRG1 anticorps (C-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement FRG1 dans WB et EIA. Il présente une réactivité envers Humain.
N° du produit ABIN952390

Aperçu rapide pour FRG1 anticorps (C-Term) (ABIN952390)

Antigène

Voir toutes FRG1 Anticorps
FRG1 (FSHD Region Gene 1 (FRG1))

Reactivité

  • 35
  • 19
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 32
  • 2
  • 1
Lapin

Clonalité

  • 33
  • 2
Polyclonal

Conjugué

  • 16
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp FRG1 est non-conjugé

Application

  • 35
  • 13
  • 13
  • 12
  • 3
  • 3
  • 3
  • 2
  • 1
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Épitope

    • 15
    • 9
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 229-257, C-Term

    Specificité

    This antibody recognizes Human FRG1 (C-term).

    Purification

    Protein A column, followed by peptide affinity purification

    Immunogène

    KLH conjugated synthetic peptide between 229-257 amino acids from the C-terminal region of Human FRG1

    Isotype

    Ig Fraction
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS containing 0.09 % (W/V) Sodium Azide as preservative

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Antigène

    FRG1 (FSHD Region Gene 1 (FRG1))

    Autre désignation

    FRG1

    Sujet

    This gene maps to a location 100 kb centromeric of the repeat units on chromosome 4q35 which are deleted in facioscapulohumeral muscular dystrophy (FSHD). It is evolutionarily conserved and has related sequences on multiple human chromosomes but DNA sequence analysis did not reveal any homology to known genes. In vivo studies demonstrate the encoded protein is localized to the nucleolus.Synonyms: FSHD region gene 1 protein

    Poids moléculaire

    29172 Da

    ID gène

    2483

    NCBI Accession

    NP_004468
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