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MANSC1 anticorps (AA 21-337)

L’anticorps anti-MANSC1 Polyclonal Lapin est utilisé pour la détection de MANSC1 dans des échantillons de Humain. Il a été validé pour WB et ELISA.
N° du produit ABIN7872165
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour MANSC1 anticorps (AA 21-337) (ABIN7872165)

Antigène

Voir toutes MANSC1 Anticorps
MANSC1 (MANSC Domain Containing 1 (MANSC1))

Reactivité

  • 23
  • 17
  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 38
Lapin

Clonalité

  • 38
Polyclonal

Conjugué

  • 12
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp MANSC1 est non-conjugé

Application

  • 30
  • 14
  • 13
  • 13
  • 4
  • 4
  • 3
  • 1
Western Blotting (WB), ELISA
  • Épitope

    • 15
    • 9
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 21-337

    Fonction

    MANSC1 Antibody / MANSC domain-containing protein 1

    Purification

    Antigen affinity purified

    Immunogène

    An E.coli-derived human recombinant protein (amino acids L21-N337) was used as the immunogen for the MANSC1 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the MANSC1 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    4 °C,-20 °C

    Stockage commentaire

    After reconstitution, the MANSC1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Antigène

    MANSC1 (MANSC Domain Containing 1 (MANSC1))

    Autre désignation

    MANSC1

    Sujet

    MANSC1 (MANSC domain-containing protein 1), also known as LOH12CR3 (Loss of heterozygosity 12 chromosomal region 3 protein), is a 414 amino acid single-pass membrane protein. Expressed throughout the body, MANSC1 contains one MANSC domain and is encoded by a gene that is located on chromosome 12. Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction.

    UniProt

    Q9H8J5
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