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

MANSC1 anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement MANSC1 dans ELISA et IHC. Il présente une réactivité envers Humain.
N° du produit ABIN7247171

Aperçu rapide pour MANSC1 anticorps (ABIN7247171)

Antigène

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

Reactivité

  • 23
  • 16
  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 37
  • 1
Lapin

Clonalité

  • 37
  • 1
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

  • 31
  • 13
  • 13
  • 13
  • 5
  • 4
  • 3
  • 3
  • 2
ELISA, Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Fusion protein of human MANSC1

    Isotype

    IgG
  • Indications d'application

    IHC 1:50-1:300, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.8 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • 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
Vous êtes ici:
Chat with us!