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FAM134B antibody

FAM134B Reactivity: Human, Mouse, Rat WB, ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7246982
  • Target See all FAM134B Antibodies
    FAM134B (Family with Sequence Similarity 134, Member B (FAM134B))
    Reactivity
    • 31
    • 21
    • 21
    • 4
    • 4
    • 4
    • 4
    • 4
    • 2
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 29
    • 2
    Rabbit
    Clonality
    • 31
    Polyclonal
    Conjugate
    • 12
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FAM134B antibody is un-conjugated
    Application
    • 26
    • 14
    • 13
    • 13
    • 8
    • 4
    • 4
    • 3
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Fusion protein of human RETREG1
    Isotype
    IgG
    Top Product
    Discover our top product FAM134B Primary Antibody
  • Application Notes
    WB 1:500-1:2000, IHC 1:50-1:300, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.02 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
    FAM134B (Family with Sequence Similarity 134, Member B (FAM134B))
    Alternative Name
    RETREG1 (FAM134B Products)
    Synonyms
    JK-1 antibody, JK1 antibody, 1810015C04Rik antibody, AU015349 antibody, reticulophagy regulator 1 antibody, family with sequence similarity 134, member B antibody, RETREG1 antibody, Retreg1 antibody, Fam134b antibody
    Background
    The protein encoded by this gene is a cis-Golgi transmembrane protein that may be necessary for the long-term survival of nociceptive and autonomic ganglion neurons. Mutations in this gene are a cause of hereditary sensory and autonomic neuropathy type IIB (HSAN IIB), and this gene may also play a role in susceptibility to vascular dementia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.
    Molecular Weight

    Observed_MW: Refer to figures

    Calculated_MW: 55 kDa

    UniProt
    Q9H6L5
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