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BBS12 antibody

BBS12 Reactivity: Human ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7254703
  • Target See all BBS12 Antibodies
    BBS12 (Bardet-Biedl Syndrome 12 (BBS12))
    Reactivity
    • 19
    • 1
    Human
    Host
    • 17
    • 2
    Rabbit
    Clonality
    • 19
    Polyclonal
    Conjugate
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This BBS12 antibody is un-conjugated
    Application
    • 19
    • 13
    • 13
    • 3
    • 3
    • 3
    • 1
    ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Synthetic peptide of human BBS12
    Isotype
    IgG
    Top Product
    Discover our top product BBS12 Primary Antibody
  • Application Notes
    IHC 1:40-1:200, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.9 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
    BBS12 (Bardet-Biedl Syndrome 12 (BBS12))
    Alternative Name
    BBS12 (BBS12 Products)
    Synonyms
    Gm1805 antibody, Gm407 antibody, Gm721 antibody, RP23-137F6.2 antibody, RGD1561608 antibody, C4orf24 antibody, DKFZP468P0511 antibody, Bardet-Biedl syndrome 12 (human) antibody, Bardet-Biedl syndrome 12 antibody, Bardet-Biedl syndrome 12 L homeolog antibody, Bbs12 antibody, BBS12 antibody, bbs12 antibody, bbs12.L antibody
    Background
    The protein encoded by this gene is part of a complex that is involved in membrane trafficking. The encoded protein is a molecular chaperone that aids in protein folding upon ATP hydrolysis. This protein also plays a role in adipocyte differentiation. Defects in this gene are a cause of Bardet-Biedl syndrome type 12. Two transcript variants encoding the same protein have been found for this gene.
    UniProt
    Q6ZW61
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