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MANSC1 Antikörper

MANSC1 Reaktivität: Human ELISA, IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7247171
  • Target Alle MANSC1 Antikörper anzeigen
    MANSC1 (MANSC Domain Containing 1 (MANSC1))
    Reaktivität
    • 25
    • 16
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Wirt
    • 40
    Kaninchen
    Klonalität
    • 40
    Polyklonal
    Konjugat
    • 9
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser MANSC1 Antikörper ist unkonjugiert
    Applikation
    • 33
    • 17
    • 13
    • 13
    • 4
    • 3
    • 3
    • 1
    ELISA, Immunohistochemistry (IHC)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Antigen affinity purification
    Immunogen
    Fusion protein of human MANSC1
    Isotyp
    IgG
    Top Product
    Discover our top product MANSC1 Primärantikörper
  • Applikationshinweise
    IHC 1:50-1:300, ELISA 1:5000-1:10000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1.8 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    MANSC1 (MANSC Domain Containing 1 (MANSC1))
    Andere Bezeichnung
    MANSC1 (MANSC1 Produkte)
    Synonyme
    MANSC1 antikoerper, DKFZp469A172 antikoerper, 9130403P13Rik antikoerper, LOH12CR3 antikoerper, MANSC domain containing 1 antikoerper, MANSC1 antikoerper, Mansc1 antikoerper, LOC777123 antikoerper
    Hintergrund
    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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