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Transducin (Beta)-Like 1X-Linked (TBL1X) (Middle Region) Peptide

TBL1X Reactivity: Human Host: Synthetic BP
Catalog No. ABIN8114221
$145.08
Plus shipping costs $50.00
100 μg
Shipping to: United States
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Quick Overview for Transducin (Beta)-Like 1X-Linked (TBL1X) (Middle Region) Peptide (ABIN8114221)

Target

TBL1X (Transducin (Beta)-Like 1X-Linked (TBL1X))

Origin

Human

Source

  • 5
Synthetic

Application

Blocking Peptide (BP)
  • Protein Region

    Middle Region

    Purpose

    TBL1X Peptide - middle region

    Sequence

    AAAAAAAATA AATAATTTSA GVSHQNPSKN REATVNGEEN RAHSVNNHAK
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Comment

    This is a synthetic peptide designed for use in combination with anti- TBL1X Antibody (ARP88707_P050),. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications. Please inquire for more details.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 µL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Buffer

    Lyophilized powder

    Storage

    -20 °C

    Storage Comment

    For longer periods of storage, store at -20 °C. Avoid repeat freeze-thaw cycles.
  • Target

    TBL1X (Transducin (Beta)-Like 1X-Linked (TBL1X))

    Background

    Background Information: The protein encoded by this gene has sequence similarity with members of the WD40 repeat-containing protein family. The WD40 group is a large family of proteins, which appear to have a regulatory function. It is believed that the WD40 repeats mediate protein-protein interactions and members of the family are involved in signal transduction, RNA processing, gene regulation, vesicular trafficking, cytoskeletal assembly and may play a role in the control of cytotypic differentiation. This encoded protein is found as a subunit in corepressor SMRT (silencing mediator for retinoid and thyroid receptors) complex along with histone deacetylase 3 protein. This gene is located adjacent to the ocular albinism gene and it is thought to be involved in the pathogenesis of the ocular albinism with late-onset sensorineural deafness phenotype. Four transcript variants encoding two different isoforms have been found for this gene. This gene is highly similar to the Y chromosome TBL1Y gene.

    Alternative Symbols: EBI, TBL1, SMAP55

    Molecular Weight

    57 kDa

    Gene ID

    6907

    NCBI Accession

    NP_001132938

    UniProt

    O60907
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