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ALDOA antibody (AA 9-145)

This anti-ALDOA antibody is a Mouse Monoclonal antibody detecting ALDOA in ELISA, ICC and FACS. Suitable for Human.
Catalog No. ABIN5611222

Quick Overview for ALDOA antibody (AA 9-145) (ABIN5611222)

Target

See all ALDOA Antibodies
ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))

Reactivity

  • 80
  • 32
  • 30
  • 17
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 60
  • 13
  • 12
  • 2
Mouse

Clonality

  • 71
  • 15
Monoclonal

Conjugate

  • 58
  • 7
  • 6
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
This ALDOA antibody is un-conjugated

Application

  • 70
  • 40
  • 26
  • 22
  • 19
  • 12
  • 9
  • 7
  • 6
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
ELISA, Immunocytochemistry (ICC), Flow Cytometry (FACS)

Clone

2H2B1
  • Binding Specificity

    • 11
    • 6
    • 6
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 9-145

    Purpose

    ALDOA Antibody

    Purification

    Purified antibody

    Immunogen

    Purified recombinant fragment of human ALDOA (AA: 9-145) expressed in E. Coli.

    Isotype

    IgG1
  • Application Notes

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    ICC: 1/100 - 1/500

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % 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

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target

    ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))

    Alternative Name

    ALDOA

    Background

    The protein encoded by this gene, Aldolase A (fructose-bisphosphate aldolase), is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development. Aldolase A is found in the developing embryo and is produced in even greater amounts in adult muscle. Aldolase A expression is repressed in adult liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Aldolase A deficiency has been associated with myopathy and hemolytic anemia. Alternative splicing and alternative promoter usage results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 3 and 10.

    Molecular Weight

    39.4 kDa

    Gene ID

    226

    UniProt

    P04075

    Pathways

    Ribonucleoside Biosynthetic Process
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