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Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B) (Middle Region) Peptide

BAZ1B Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN973746
  • Target See all BAZ1B products
    BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
    Protein Region
    Middle Region
    Origin
    Human
    Source
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Characteristics
    This is a synthetic peptide designed for use in combination with anti-BAZ1B antibody (Catalog #: ARP39571_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.
    Purification
    Purified
  • Application Notes
    Each Investigator should determine their own optimal working dilution for specific applications.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Concentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handling Advice
    Avoid repeated freeze-thaw cycles.
    Storage
    -20 °C
    Storage Comment
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
    Synonyms
    BAZ1B Peptide, wstf Peptide, wbscr9 Peptide, wbscr10 Peptide, LOC100220420 Peptide, WBSCR10 Peptide, WBSCR9 Peptide, WSTF Peptide, C87820 Peptide, Wbscr9 Peptide, fi60d02 Peptide, im:7137554 Peptide, wu:fi60d02 Peptide, bromodomain adjacent to zinc finger domain 1B Peptide, bromodomain adjacent to zinc finger domain, 1B Peptide, bromodomain adjacent to zinc finger domain 1B S homeolog Peptide, BAZ1B Peptide, baz1b Peptide, Baz1b Peptide, baz1b.S Peptide
    Background
    BAZ1B is a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23.This gene encodes a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

    Alias Symbols: WBSCR10, WBSCR9, WSTF

    Protein Interaction Partner: PCNA,MYO1C,PCNA,SMARCA1,SMARCA5,SMARCC2,SMARCE1,ACTL6A,ARID1A,BAZ1A,CDT1,CHAF1B,ESR1,SMARCA5,SMARCB1,SMARCC1,SMARCC2,SMARCD1,SMARCE1,SUPT16H,TOP2B,TRNAG1,VDR

    Protein Size: 1483
    Molecular Weight
    171 kDa
    Gene ID
    9031
    NCBI Accession
    NM_032408, NP_115784
    UniProt
    Q9UIG0
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