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BBS12 antibody

The Rabbit Polyclonal anti-BBS12 antibody has been validated for WB. It is suitable to detect BBS12 in samples from Human.
Catalog No. ABIN2854610

Quick Overview for BBS12 antibody (ABIN2854610)

Target

See all BBS12 Antibodies
BBS12 (Bardet-Biedl Syndrome 12 (BBS12))

Reactivity

  • 24
  • 1
Human

Host

  • 22
  • 2
Rabbit

Clonality

  • 24
Polyclonal

Conjugate

  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This BBS12 antibody is un-conjugated

Application

  • 18
  • 13
  • 13
  • 3
  • 3
  • 3
  • 1
Western Blotting (WB)
  • Cross-Reactivity

    Human

    Characteristics

    Rabbit polyclonal antibody to BBS12 (Bardet-Biedl syndrome 12)
    FLJ35630 antibody [C1C3]

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human BBS12. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: HepG2

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

    BBS12 (Bardet-Biedl Syndrome 12 (BBS12))

    Alternative Name

    Bardet-Biedl syndrome 12

    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.

    Molecular Weight

    79 kDa

    Gene ID

    166379

    UniProt

    Q6ZW61
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