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PFKM antibody (N-Term)

This anti-PFKM antibody is a Rabbit Polyclonal antibody detecting PFKM in WB and IHC (p). Suitable for Human.
Catalog No. ABIN392748

Quick Overview for PFKM antibody (N-Term) (ABIN392748)

Target

See all PFKM Antibodies
PFKM (phosphofructokinase, Muscle (PFKM))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This PFKM antibody is un-conjugated

Application

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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB3905
  • Binding Specificity

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    AA 122-151, N-Term

    Purification

    This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

    Immunogen

    This Fructose 6 Phosphate Kinase antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 122-151 amino acids from the N-terminal region of human Fructose 6 Phosphate Kinase.

    Isotype

    Ig Fraction
  • Application Notes

    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

    PFKM (phosphofructokinase, Muscle (PFKM))

    Alternative Name

    Fructose 6 Phosphate Kinase (PFKM)

    Background

    Phosphofructokinase catalyzes the irreversible conversion of fructose 6 phosphate to fructose 1,6 bisphosphate. Mammalian PFK is a complex isozyme consisting of 3 subunits: muscle (M), liver (L), and platelet (P). Only M type PFK isozyme is expressed in mature muscle, while erythrocytes contain both L and M subunits. Defects in PFKM are the cause of glycogen storage disease type 7 (GSD7), also known as Tarui disease.

    Molecular Weight

    85183

    Gene ID

    5213

    NCBI Accession

    NP_000280, NP_001160158, NP_001160159, NP_001160160

    UniProt

    P08237

    Pathways

    Positive Regulation of Peptide Hormone Secretion, Negative Regulation of Hormone Secretion, Carbohydrate Homeostasis, Warburg Effect
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