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Thyroid Hormone Receptor Interactor 4 (TRIP4) (Middle Region) Peptide

TRIP4 Reactivity: Human Host: Synthetic BP
Catalog No. ABIN8113872
$145.08
Plus shipping costs $50.00
100 μg
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Quick Overview for Thyroid Hormone Receptor Interactor 4 (TRIP4) (Middle Region) Peptide (ABIN8113872)

Target

TRIP4 (Thyroid Hormone Receptor Interactor 4 (TRIP4))

Origin

Human

Source

  • 10
Synthetic

Application

Blocking Peptide (BP)
  • Protein Region

    Middle Region

    Purpose

    TRIP4 Peptide - middle region

    Sequence

    FKKDEILDGQ KSGDHLKRGR KKGRNRQEVP AFTEPDTTAE VKTPFDLAKA
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Comment

    This is a synthetic peptide designed for use in combination with anti- TRIP4 Antibody (ARP85792_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

    TRIP4 (Thyroid Hormone Receptor Interactor 4 (TRIP4))

    Background

    Background Information: This gene encodes a subunit of the tetrameric nuclear activating signal cointegrator 1 (ASC-1) complex, which associates with transcriptional coactivators, nuclear receptors and basal transcription factors to facilitate nuclear receptors-mediated transcription. This protein is localized in the nucleus and contains an E1A-type zinc finger domain, which mediates interaction with transcriptional coactivators and ligand-bound nuclear receptors, such as thyroid hormone receptor and retinoid X receptor alpha, but not glucocorticoid receptor. Mutations in this gene are associated with spinal muscular atrophy with congenital bone fractures-1 (SMABF1).  

    Alternative Symbols: ASC1, ASC-1, ZC2HC5, HsT17391

    Molecular Weight

    63 kDa

    Gene ID

    9325

    NCBI Accession

    NP_057297

    UniProt

    Q15650
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