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TMEM158 anticorps

TMEM158 Reactivité: Souris WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7075993
  • Antigène Voir toutes TMEM158 Anticorps
    TMEM158 (Transmembrane Protein 158 (TMEM158))
    Reactivité
    • 31
    • 17
    • 3
    • 1
    • 1
    Souris
    Hôte
    • 32
    Lapin
    Clonalité
    • 32
    Polyclonal
    Conjugué
    • 7
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp TMEM158 est non-conjugé
    Application
    • 32
    • 15
    • 13
    • 13
    • 3
    • 3
    • 2
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogène
    Recombinant protein corresponding to Mouse TMEM158
    Top Product
    Discover our top product TMEM158 Anticorps primaire
  • Indications d'application
    WB (M) 1:500-1:1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS, pH 7.4, 0.02 % sodium azide
    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
  • Antigène
    TMEM158 (Transmembrane Protein 158 (TMEM158))
    Autre désignation
    TMEM158 (TMEM158 Produits)
    Synonymes
    anticorps 2310037P21Rik, anticorps Ris1, anticorps BBP, anticorps RIS1, anticorps p40BBP, anticorps transmembrane protein 158, anticorps transmembrane protein 158 (gene/pseudogene), anticorps Tmem158, anticorps TMEM158
    Sujet
    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.
    Poids moléculaire
    35 kDa
    UniProt
    Q6F5E0
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