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MYST Histone Acetyltransferase (Monocytic Leukemia) 3 (MYST3) (N-Term) Peptide

MYST3 Reactivity: Human Host: Synthetic BP
Catalog No. ABIN8106033
$145.08
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for MYST Histone Acetyltransferase (Monocytic Leukemia) 3 (MYST3) (N-Term) Peptide (ABIN8106033)

Target

MYST3 (MYST Histone Acetyltransferase (Monocytic Leukemia) 3 (MYST3))

Origin

Human

Source

  • 3
Synthetic

Application

Blocking Peptide (BP)
  • Protein Region

    N-Term

    Purpose

    KAT6A Peptide - N-terminal region

    Sequence

    GLDRKTVLEQ LELSVKDGTI LKVSNKGLNS YKDPDNPGRI ALPKPRNHGK
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Comment

    This is a synthetic peptide designed for use in combination with anti-MYST3 Antibody (ARP79525_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

    MYST3 (MYST Histone Acetyltransferase (Monocytic Leukemia) 3 (MYST3))

    Background

    Background Information: This gene encodes a member of the MOZ, YBFR2, SAS2, TIP60 family of histone acetyltransferases. The protein is composed of a nuclear localization domain, a double C2H2 zinc finger domain that binds to acetylated histone tails, a histone acetyl-transferase domain, a glutamate/aspartate-rich region, and a serine- and methionine-rich transactivation domain. It is part of a complex that acetylates lysine-9 residues in histone 3, and in addition, it acts as a co-activator for several transcription factors. Allelic variants of this gene are associated with an autosomal dominant form of cognitive disability. Chromosomal translocations of this gene are associated with acute myeloid leukemia. Alternative splicing results in multiple transcript variants.

    Alternative Symbols: MOZ, MRD32, MYST3, MYST-3, ZNF220, RUNXBP2, ZC2HC6A

    Molecular Weight

    89 kDa

    Gene ID

    7994

    NCBI Accession

    NP_006757

    UniProt

    A5PLL3
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