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PKLR antibody (N-Term)

This anti-PKLR antibody is a Rabbit Polyclonal antibody detecting PKLR in WB and IHC (p). Suitable for Human.
Catalog No. ABIN391050

Quick Overview for PKLR antibody (N-Term) (ABIN391050)

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
  • 35
  • 32
  • 10
  • 10
  • 5
  • 4
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB03692
  • Binding Specificity

    • 15
    • 7
    • 6
    • 5
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-30, N-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This PKLR antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human PKLR.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000. WB: 1:1000. IHC-P: 1:50~100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    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

    4 °C,-20 °C

    Storage Comment

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Expiry Date

    6 months
  • Target

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

    Alternative Name

    PKLR

    Background

    PKLR is a pyruvate kinase that catalyzes the production of phosphoenolpyruvate from pyruvate and ATP. Defects in this enzyme, due to gene mutations or genetic variations, are the common cause of chronic hereditary nonspherocytic hemolytic anemia (CNSHA or HNSHA).

    Molecular Weight

    61830

    Gene ID

    5313

    NCBI Accession

    NP_000289, NP_870986

    UniProt

    P30613

    Pathways

    Ribonucleoside Biosynthetic Process
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