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MANSC1 anticorps

MANSC1 Reactivité: Humain ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7247171
  • Antigène Voir toutes MANSC1 Anticorps
    MANSC1 (MANSC Domain Containing 1 (MANSC1))
    Reactivité
    • 25
    • 16
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 40
    Lapin
    Clonalité
    • 40
    Polyclonal
    Conjugué
    • 9
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp MANSC1 est non-conjugé
    Application
    • 33
    • 17
    • 13
    • 13
    • 4
    • 3
    • 3
    • 1
    ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogène
    Fusion protein of human MANSC1
    Isotype
    IgG
    Top Product
    Discover our top product MANSC1 Anticorps primaire
  • 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 (MANSC1 Produits)
    Synonymes
    anticorps MANSC1, anticorps DKFZp469A172, anticorps 9130403P13Rik, anticorps LOH12CR3, anticorps MANSC domain containing 1, anticorps MANSC1, anticorps Mansc1, anticorps LOC777123
    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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