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PKLR antibody (AA 1-230)

This Rabbit Polyclonal antibody specifically detects PKLR in WB, IHC and IF. It exhibits reactivity toward Human.
Catalog No. ABIN1885816

Quick Overview for PKLR antibody (AA 1-230) (ABIN1885816)

Target

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

Reactivity

  • 62
  • 31
  • 23
  • 6
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 62
  • 12
Rabbit

Clonality

  • 64
  • 10
Polyclonal

Conjugate

  • 42
  • 6
  • 6
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
This PKLR antibody is un-conjugated

Application

  • 49
  • 34
  • 32
  • 10
  • 10
  • 5
  • 4
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Binding Specificity

    • 15
    • 7
    • 7
    • 5
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-230

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 230 of Pyruvate Kinase(liver/RBC)
  • Application Notes

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.50-1.500
    Immunofluorescence: 1.100-1.200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target

    PKLR (Pyruvate Kinase, Liver and RBC (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.[provided by RefSeq]

    Molecular Weight

    62 kDa

    Gene ID

    5313

    NCBI Accession

    NM_000298, NP_000289

    Pathways

    Ribonucleoside Biosynthetic Process
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