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ERLIN1 antibody

ERLIN1 Reactivity: Human, Mouse, Rat ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7247786
  • Target See all ERLIN1 Antibodies
    ERLIN1 (ER Lipid Raft Associated 1 (ERLIN1))
    Reactivity
    • 29
    • 7
    • 6
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 28
    • 1
    Rabbit
    Clonality
    • 29
    Polyclonal
    Conjugate
    • 15
    • 4
    • 3
    • 3
    • 2
    • 2
    This ERLIN1 antibody is un-conjugated
    Application
    • 24
    • 19
    • 18
    • 3
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Fusion protein of human ERLIN1
    Isotype
    IgG
    Top Product
    Discover our top product ERLIN1 Primary Antibody
  • Application Notes
    IHC 1:50-1:200, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.72 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    ERLIN1 (ER Lipid Raft Associated 1 (ERLIN1))
    Alternative Name
    ERLIN1 (ERLIN1 Products)
    Synonyms
    C10orf69 antibody, Erlin-1 antibody, KE04 antibody, KEO4 antibody, SPFH1 antibody, wu:fa10h05 antibody, wu:fb19h05 antibody, zgc:110547 antibody, 2810439N09Rik antibody, C80197 antibody, Keo4 antibody, Spfh1 antibody, RGD1307058 antibody, erlin-1 antibody, ER lipid raft associated 1 antibody, ERLIN1 antibody, erlin1 antibody, Erlin1 antibody
    Background
    The protein encoded by this gene is part of a protein complex that mediates degradation of inositol 1,4,5-trisphosphate receptors in the endoplasmic reticulum. The encoded protein also binds cholesterol and regulates the SREBP signaling pathway, which promotes cellular cholesterol homeostasis. Defects in this gene have been associated with spastic paraplegia 62.
    UniProt
    O75477
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