Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

ST7 anticorps (AA 268-309)

ST7 Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN5708171
  • Antigène Voir toutes ST7 Anticorps
    ST7 (Suppression of Tumorigenicity 7 (ST7))
    Épitope
    • 9
    • 7
    • 7
    • 6
    • 2
    • 1
    • 1
    AA 268-309
    Reactivité
    • 21
    • 3
    • 3
    Humain
    Hôte
    • 21
    • 1
    Lapin
    Clonalité
    • 22
    Polyclonal
    Conjugué
    • 12
    • 2
    • 2
    • 2
    • 2
    • 2
    Cet anticorp ST7 est non-conjugé
    Application
    • 21
    • 16
    • 14
    • 3
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Antigen affinity purified
    Immunogène
    Amino acids 268-309 (DGCYRRSQQLQHHGSQYEAQHRRDTNVLVYIKRRLAMCARRL-human) were used as the immunogen for the ST7 antibody.
    Isotype
    IgG
    Top Product
    Discover our top product ST7 Anticorps primaire
  • Indications d'application
    Optimal dilution of the ST7 antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL
    Restrictions
    For Research Use only
  • Buffer
    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
    Stock
    -20 °C
    Stockage commentaire
    After reconstitution, the ST7 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Antigène
    ST7 (Suppression of Tumorigenicity 7 (ST7))
    Autre désignation
    Suppressor of Tumorigenicity 7 (ST7 Produits)
    Synonymes
    anticorps ETS7q, anticorps FAM4A, anticorps FAM4A1, anticorps HELG, anticorps RAY1, anticorps SEN4, anticorps TSG7, anticorps 9430001H04Rik, anticorps Fam4a2, anticorps suppression of tumorigenicity 7, anticorps ST7, anticorps St7
    Sujet
    Suppressor of tumorigenicity protein 7 is a protein that in humans is encoded by the ST7 gene. 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.
    UniProt
    Q9NRC1
Vous êtes ici:
Support technique