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ST7 anticorps (AA 169-197)

Cet anticorps anti-ST7 est un anticorps Lapin Polyclonal détectant ST7 dans WB et FACS. Adapté pour Humain.
N° du produit ABIN5532994

Aperçu rapide pour ST7 anticorps (AA 169-197) (ABIN5532994)

Antigène

Voir toutes ST7 Anticorps
ST7 (Suppression of Tumorigenicity 7 (ST7))

Reactivité

  • 16
  • 4
  • 4
Humain

Hôte

  • 16
  • 1
Lapin

Clonalité

  • 17
Polyclonal

Conjugué

  • 11
  • 2
  • 1
  • 1
  • 1
  • 1
Cet anticorp ST7 est non-conjugé

Application

  • 16
  • 12
  • 11
  • 3
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS)
  • Épitope

    • 8
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    AA 169-197

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This ST7 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 169-197 amino acids from the Central region of human ST7.

    Isotype

    Ig Fraction
  • Indications d'application

    For WB starting dilution is: 1:1000

    For FACS starting dilution is: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Buffer

    Supplied in PBS with 0.09 % (W/V) sodium azide.

    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.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Antigène

    ST7 (Suppression of Tumorigenicity 7 (ST7))

    Autre désignation

    ST7

    Sujet

    The gene for this product maps to a region on chromosome 7 identified as an autism-susceptibility locus. Mutation screening of the entire coding region in autistic individuals failed to identify phenotype-specific variants, suggesting that coding mutations for this gene are unlikely to be involved in the etiology of autism. The function of this gene product has not been determined. Transcript variants encoding different isoforms of this protein have been described.

    Poids moléculaire

    67 kDa

    ID gène

    7982

    UniProt

    Q9NRC1
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