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PKLR antibody (AA 446-556)

This Rabbit Polyclonal antibody specifically detects PKLR in WB. It exhibits reactivity toward Human.
Catalog No. ABIN6145710

Quick Overview for PKLR antibody (AA 446-556) (ABIN6145710)

Target

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

Reactivity

  • 61
  • 30
  • 22
  • 6
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 59
  • 12
Rabbit

Clonality

  • 61
  • 10
Polyclonal

Conjugate

  • 39
  • 6
  • 6
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
This PKLR antibody is un-conjugated

Application

  • 46
  • 32
  • 32
  • 9
  • 7
  • 6
  • 5
  • 2
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 14
    • 7
    • 7
    • 5
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 446-556

    Sequence

    PLSRDPTEVT AIGAVEAAFK CCAAAIIVLT TTGRSAQLLS RYRPRAAVIA VTRSAQAARQ VHLCRGVFPL LYREPPEAIW ADDVDRRVQF GIESGKLRGF LRVGDLVIVV T

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 446-556 of human PKLR (NP_000289.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Comment

    HIGH QUALITY

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • 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.,PKLR,PK1,PKL,PKR,PKRL,RPK,Cancer,Signal Transduction,Endocrine & Metabolism,Carbohydrate metabolism,PKLR

    Molecular Weight

    58 kDa/61 kDa

    Gene ID

    5313

    UniProt

    P30613

    Pathways

    Ribonucleoside Biosynthetic Process
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