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

Recombinant PKLR protein expressed in HEK-293 Cells.
Catalog No. ABIN2729045
$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 PKLR Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag) (ABIN2729045)

Target

See all PKLR Proteins
PKLR (Pyruvate Kinase, Liver and RBC (PKLR))

Protein Type

Recombinant

Origin

  • 13
  • 4
  • 3
  • 1
  • 1
Human

Source

  • 9
  • 4
  • 3
  • 2
  • 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 PKLR protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human PKLR (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
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    Product
    Expression System
    Conjugate
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    Expression System HEK-293 Cells
    Conjugate His tag
    Origin Human
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    Conjugate Strep Tag
    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

    PKLR (Pyruvate Kinase, Liver and RBC (PKLR))

    Alternative Name

    Pklr

    Background

    The protein encoded by this gene is a pyruvate kinase that catalyzes the transphosphorylation of phohsphoenolpyruvate into pyruvate and ATP, which is the rate-limiting step of glycolysis. Defects in this enzyme, due to gene mutations or genetic variations, are the common cause of chronic hereditary nonspherocytic hemolytic anemia (CNSHA or HNSHA). Multiple transcript variants encoding different isoforms have been found for this gene.

    Molecular Weight

    61.6 kDa

    NCBI Accession

    NP_000289

    Pathways

    Ribonucleoside Biosynthetic Process
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