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TMEM158 Antikörper

TMEM158 Reaktivität: Maus WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7075993
  • Target Alle TMEM158 Antikörper anzeigen
    TMEM158 (Transmembrane Protein 158 (TMEM158))
    Reaktivität
    • 31
    • 17
    • 3
    • 1
    • 1
    Maus
    Wirt
    • 32
    Kaninchen
    Klonalität
    • 32
    Polyklonal
    Konjugat
    • 7
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser TMEM158 Antikörper ist unkonjugiert
    Applikation
    • 32
    • 15
    • 13
    • 13
    • 3
    • 3
    • 2
    • 1
    Western Blotting (WB)
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant protein corresponding to Mouse TMEM158
    Top Product
    Discover our top product TMEM158 Primärantikörper
  • Applikationshinweise
    WB (M) 1:500-1:1000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    PBS, pH 7.4, 0.02 % sodium azide
    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
  • Target
    TMEM158 (Transmembrane Protein 158 (TMEM158))
    Andere Bezeichnung
    TMEM158 (TMEM158 Produkte)
    Synonyme
    2310037P21Rik antikoerper, Ris1 antikoerper, BBP antikoerper, RIS1 antikoerper, p40BBP antikoerper, transmembrane protein 158 antikoerper, transmembrane protein 158 (gene/pseudogene) antikoerper, Tmem158 antikoerper, TMEM158 antikoerper
    Hintergrund
    TMEM158 is a 286 amino acid protein encoded by a gene mapping to human chromosome 3. Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
    Molekulargewicht
    35 kDa
    UniProt
    Q6F5E0
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