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WHSC1 Protein (DYKDDDDK Tag)

This Recombinant WHSC1 protein is produced in Baculovirus.
Catalog No. ABIN2669701
$641.54
Plus shipping costs $50.00, if applicable $20.00 dry ice
20 μg
Shipping to: United States
Delivery in 1 to 3 Business Days

Quick Overview for WHSC1 Protein (DYKDDDDK Tag) (ABIN2669701)

Target

See all WHSC1 Proteins
WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1))

Protein Type

Recombinant

Origin

  • 5
  • 2
Human

Source

  • 2
  • 2
  • 2
  • 1
Baculovirus

Application

Enzyme Activity Assay (EAA), Screening Assay (ScA)
  • Purification tag / Conjugate

    This WHSC1 protein is labelled with DYKDDDDK Tag.

    Characteristics

    Recombinant MMSET / WHSC1 (accession number NP_579877.1) was expressed in Sf9 cells and contains an N-terminal FLAG tag with an observed molecular weight of 154 kDa.
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  • Application Notes

    Recombinant MMSET / WHSC1 is suitable for use in the study of enzyme kinetics, inhibitor screening, and selectivity profiling. Specific Activity: H3K36me2 methyltransferase activity. HMT Assay Conditions: 50 mM TrisCl, pH 8.6, 0.02 % Triton X-100, 2 mM MgCl2, 1 mM TCEP, 100 μM SAM, 30 ng/μl Recombinant Nucleosomes, 30 ng/μl Recombinant MMSET / WHSC1 protein at 2 hours at room temperature. Activity was detected by fluorography.

    Restrictions

    For Research Use only
  • Handling Advice

    Avoid repeated freeze/thaw cycles and keep on ice when not in storage.

    Storage

    -80 °C

    Storage Comment

    Recombinant proteins in solution are temperature sensitive and must be stored at -80°C to prevent degradation.
  • Target

    WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1))

    Alternative Name

    MMSET / WHSC1

    Background

    MMSET (Multiple Myeloma SET domain-containing protein) / WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1, also known as NSD2, Nuclear Receptor binding SET domain protein 2, TRX5, Trithorax 5) is a SET domain-containing histone methyltransferase specific for lysine 36 of histone H3. The MMSET / WHSC1 gene is deleted in Wolf-Hirschhorn syndrome, a disorder characterized by developmental defects and mental retardation. In 15 % of patients with Multiple Myeloma (MM), a chromosomal translocation leads to MMSET / WHSC1 gene being aberrantly placed under the control of the IgH intronic μ enhancer and expressed at very high levels. This event is apparently a key component in cellular transformation leading to MM. Reduction in MMSET / WHSC1 expression in a myeloma cell line suppressed its growth, suggesting a role for MMSET in maintaining the transformed state.

    Molecular Weight

    154 kDa

    Pathways

    SARS-CoV-2 Protein Interactome
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