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TMEM158 antibody

TMEM158 Reactivity: Mouse WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7075993
  • Target See all TMEM158 Antibodies
    TMEM158 (Transmembrane Protein 158 (TMEM158))
    Reactivity
    • 31
    • 17
    • 3
    • 1
    • 1
    Mouse
    Host
    • 32
    Rabbit
    Clonality
    • 32
    Polyclonal
    Conjugate
    • 7
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This TMEM158 antibody is un-conjugated
    Application
    • 32
    • 15
    • 13
    • 13
    • 3
    • 3
    • 2
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogen
    Recombinant protein corresponding to Mouse TMEM158
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    Discover our top product TMEM158 Primary Antibody
  • Application Notes
    WB (M) 1:500-1:1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS, pH 7.4, 0.02 % sodium azide
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
  • Target
    TMEM158 (Transmembrane Protein 158 (TMEM158))
    Alternative Name
    TMEM158 (TMEM158 Products)
    Synonyms
    2310037P21Rik antibody, Ris1 antibody, BBP antibody, RIS1 antibody, p40BBP antibody, transmembrane protein 158 antibody, transmembrane protein 158 (gene/pseudogene) antibody, Tmem158 antibody, TMEM158 antibody
    Background
    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.
    Molecular Weight
    35 kDa
    UniProt
    Q6F5E0
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