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Read our guarantee »Products:Signal Transduction >> Metabolism >> Energy Metabolism
Anti-Aldolase antibody
See all Aldolase products (11) ...
Mouse monoclonal to Aldolase
WB, ICC/IFmore details
Reacts with
Human
Recombinant full length protein, corresponding to amino acids 1-365 of Human Aldolase
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: None
PBS, pH 7.2
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Protein G purified
Monoclonal
IgG2b
kappa
Cancer >> Cancer Metabolism >> Metabolic signaling pathway >> Metabolism of carbohydrates
Signal Transduction >> Metabolism >> Energy Metabolism
Our Abpromise guarantee covers the use of ab54763 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: Use a concentration of 1 - 5 µg/ml.Predicted molecular weight: 39 kDa.
ICC/IF: Use a concentration of 10 µg/ml
This gene product, 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 of this gene results in multiple transcript variants which encode the same protein.
Cytoplasmic
Western blot - Aldolase antibody (ab54763)

Aldolase antibody (ab54763) at 1ug/lane + IMR-32 cell lysate at 25ug/lane.
Immunocytochemistry/ Immunofluorescence-Aldolase antibody(ab54763)

ab54763 at 10 ug/ml staining Aldolase in human Hela cells by Immunocytochemistry / Immunofluorescence.
ab54763 has not yet been referenced specifically in any publications.
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