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SMC1A anticorps (AA 59-1233)

Cet anticorps anti-SMC1A Polyclonal Lapin (ABIN7602089) détecte spécifiquement SMC1A dans WB, ELISA, IF et ICC. L’anticorps est réactif avec des échantillons de Humain.
N° du produit ABIN7602089
500,50 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 8 à 11 jours ouvrables

Aperçu rapide pour SMC1A anticorps (AA 59-1233) (ABIN7602089)

Antigène

Voir toutes SMC1A Anticorps
SMC1A (Structural Maintenance of Chromosomes 1A (SMC1A))

Reactivité

  • 156
  • 67
  • 34
  • 7
  • 7
  • 6
  • 5
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Humain

Hôte

  • 136
  • 15
  • 4
  • 1
Lapin

Clonalité

  • 99
  • 57
Polyclonal

Conjugué

  • 73
  • 9
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Cet anticorp SMC1A est non-conjugé

Application

  • 128
  • 57
  • 39
  • 38
  • 35
  • 29
  • 28
  • 24
  • 22
  • 11
  • 7
  • 4
  • 4
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunocytochemistry (ICC)
  • Épitope

    • 38
    • 16
    • 16
    • 14
    • 12
    • 8
    • 8
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 59-1233

    Fonction

    Anti-SMC1A Antibody

    Réactivité croisée (Details)

    No cross-reactivity with other proteins.

    Attributs du produit

    Anti-SMC1A Antibody (ABIN7602089). Tested in ELISA, IF, ICC, WB applications. This antibody reacts with Human. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

    Purification

    Immunogen affinity purified.

    Immunogène

    E.coli-derived human SMC1A recombinant protein (Position: K59-Q1233).

    Isotype

    IgG
  • Indications d'application

    Western blot, 0.25-0.5 μg/mL, Human
    Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human
    ELISA, 0.1-0.5 μg/mL, -

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • Antigène

    SMC1A (Structural Maintenance of Chromosomes 1A (SMC1A))

    Autre désignation

    SMC1A

    Sujet

    Synonyms: Mucin-6, MUC-6, Gastric mucin-6, MUC6

    Tissue Specificity: Expressed in the regenerative zone of gastric antrum, gastric body mucosa and gastric incisura mucosa. Expressed in the deeper mucous glands of gastric antrum. Overexpressed in Helicobacter pylori infected gastric epithelium. Highly expressed in duodenal Brunner's glands, gall bladder, seminal vesicle, pancreatic centroacinar cells and ducts, and periductal glands of the common bile duct.

    Background: Structural maintenance of chromosomes protein 1A (SMC1A) is a protein that in humans is encoded by the SMC1A gene. Proper cohesion of sister chromatids is a prerequisite for the correct segregation of chromosomes during cell division. The cohesin multiprotein complex is required for sister chromatid cohesion. This complex is composed partly of two structural maintenance of chromosomes (SMC) proteins, SMC3 and either SMC1B or the protein encoded by this gene. Most of the cohesin complexes dissociate from the chromosomes before mitosis, although those complexes at the kinetochore remain. Therefore, the encoded protein is thought to be an important part of functional kinetochores. In addition, this protein interacts with BRCA1 and is phosphorylated by ATM, indicating a potential role for this protein in DNA repair. This gene, which belongs to the SMC gene family, is located in an area of the X-chromosome that escapes X inactivation. Mutations in this gene result in Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms.

    Poids moléculaire

    150 kDa

    ID gène

    8243

    UniProt

    Q14683

    Pathways

    Stem Cell Maintenance
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