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TBL2 antibody (N-Term)

This anti-TBL2 antibody is a Rabbit Polyclonal antibody detecting TBL2 in WB and EIA. Suitable for Human.
Catalog No. ABIN955107

Quick Overview for TBL2 antibody (N-Term) (ABIN955107)

Target

See all TBL2 Antibodies
TBL2 (Transducin (Beta)-Like 2 (TBL2))

Reactivity

  • 22
  • 4
  • 2
  • 2
  • 2
Human

Host

  • 20
  • 2
Rabbit

Clonality

  • 22
Polyclonal

Conjugate

  • 17
  • 1
  • 1
  • 1
  • 1
  • 1
This TBL2 antibody is un-conjugated

Application

  • 21
  • 11
  • 11
  • 3
  • 3
  • 2
  • 2
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Binding Specificity

    • 8
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 50-80, N-Term

    Specificity

    This antibody reacts to TBL2.

    Cross-Reactivity (Details)

    Species reactivity (tested):Human.

    Purification

    Affinity chromatography on Protein A

    Immunogen

    KLH conjugated synthetic peptide between 50-80 amino acids from the N-terminal region of human TBL2

    Isotype

    Ig Fraction
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS, 0.09 % (W/V) 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.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    TBL2 (Transducin (Beta)-Like 2 (TBL2))

    Alternative Name

    TBL2

    Background

    This gene encodes a member of the beta-transducin protein family. Most proteins of the beta-transducin family are involved in regulatory functions. This protein is possibly involved in some intracellular signaling pathway. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23.Synonyms: Transducin beta-like protein 2, WBSCR13, WS beta-transducin repeats protein, Williams-Beuren syndrome chromosomal region 13 protein

    Molecular Weight

    49798 Da

    Gene ID

    26608

    NCBI Accession

    NP_036585
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