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PRDM16 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

This Recombinant PRDM16 protein is expressed in HEK-293 Cells.
Catalog No. ABIN2729560
$956.40
Plus shipping costs $50.00, if applicable $20.00 dry ice
20 μg
Shipping to: United States
Delivery in 11 to 12 Business Days

Quick Overview for PRDM16 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag) (ABIN2729560)

Target

See all PRDM16 Proteins
PRDM16 (PR Domain Containing 16 (PRDM16))

Protein Type

Recombinant

Origin

  • 2
  • 1
  • 1
Human

Source

  • 2
  • 1
  • 1
HEK-293 Cells

Application

Antibody Production (AbP), Standard (STD)

Purity

> 80 % as determined by SDS-PAGE and Coomassie blue staining
  • Protein Characteristics

    Transcript Variant 1

    Purification tag / Conjugate

    This PRDM16 protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human PRDM16 (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
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    Origin Human
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  • Application Notes

    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays

    Comment

    The tag is located at the C-terminal.

    Restrictions

    For Research Use only
  • Concentration

    50 μg/mL

    Buffer

    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

    Storage

    -80 °C

    Storage Comment

    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target

    PRDM16 (PR Domain Containing 16 (PRDM16))

    Alternative Name

    Prdm16

    Background

    The reciprocal translocation t(13)(p36q21) occurs in a subset of myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). This gene is located near the 1p36.3 breakpoint and has been shown to be specifically expressed in the t(1:3)(p36,q21)-positive MDS/AML. The protein encoded by this gene is a zinc finger transcription factor and contains an N-terminal PR domain. The translocation results in the overexpression of a truncated version of this protein that lacks the PR domain, which may play an important role in the pathogenesis of MDS and AML. Alternatively spliced transcript variants encoding distinct isoforms have been reported.

    Molecular Weight

    140.1 kDa

    NCBI Accession

    NP_071397

    Pathways

    Stem Cell Maintenance, Brown Fat Cell Differentiation
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