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ALDOA Protein (Transcript Variant 1) (His tag)

Recombinant ALDOA protein expressed in Escherichia coli (E. coli).
Catalog No. ABIN2714558
$402.00
Plus shipping costs $50.00, if applicable $20.00 dry ice
10 μg
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Quick Overview for ALDOA Protein (Transcript Variant 1) (His tag) (ABIN2714558)

Target

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

Protein Type

Recombinant

Origin

  • 12
  • 3
  • 1
  • 1
  • 1
  • 1
Human

Source

  • 7
  • 5
  • 4
  • 1
  • 1
Escherichia coli (E. coli)

Application

Antibody Production (AbP), Standard (STD)

Purity

> 95 % as determined by SDS-PAGE and Coomassie blue staining
  • Protein Characteristics

    Transcript Variant 1

    Purification tag / Conjugate

    This ALDOA protein is labelled with His tag.

    Characteristics

    • Recombinant human Aldolase A / ALDOA (transcript variant 1) protein expressed in E. coli.
    • Produced with end-sequenced ORF clone

    Endotoxin Level

    < 0.1 EU per μg protein as determined by LAL test
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  • Application Notes

    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays

    Comment

    The tag is located at the C-terminal.

    Restrictions

    For Research Use only
  • Concentration

    50 μg/mL

    Buffer

    20 mM Tris-HCl, 100 mM NaCl, 20 % Glycerol, pH 8.0. Avoid repeated freeze-thaw cycles. Stable for at least 3 months from receipt of products under proper storage and handling conditions.

    Storage

    -80 °C

    Storage Comment

    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target

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

    Alternative Name

    Aldolase A,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

    40.5 kDa

    NCBI Accession

    NP_000025

    Pathways

    Ribonucleoside Biosynthetic Process
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