Cat#:PA-4085F;Product Name:Goat Anti-Aldolase, Rabbit Muscle Antibody;Synonym:ALDA; ALDOA; Aldolase A; Aldolase A fructose bisphosphatase; Aldolase A fructose bisphosphate; Lung cancer antigen NY LU 1; Fructose 1 6 bisphosphate triosephosphate lyase; Fructose bisphosphate aldolase A; Fructose bisphosphate aldolase; MGC10942; GSD12; MGC17716; MGC17767; Muscle type aldolase; EC 4.1.2.13; OTTHUMP00000162984; Muscle-type aldolase; Lung cancer antigen NY-LU-1; Aldolase; Aldolase;Background: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.;Description:Goat Anti-Aldolase, Rabbit Muscle Polyclonal Antibody;Host Species:Goat;Species Reactivity:Rabbit;Application:ELISA, IEP, WB;Storage:Store antibody products at 2-8°C. For long term storage, aliquot and freeze at -20°C. Avoid repeated freeze/thaw cycles;Usage:For Lab Research Use Only;
ALDA; ALDOA; Aldolase A; Aldolase A fructose bisphosphatase; Aldolase A fructose bisphosphate; Lung cancer antigen NY LU 1; Fructose 1 6 bisphosphate triosephosphate lyase; Fructose bisphosphate aldolase A; Fructose bisphosphate aldolase; MGC10942; GSD12; MGC17716; MGC17767; Muscle type aldolase; EC 4.1.2.13; OTTHUMP00000162984; Muscle-type aldolase; Lung cancer antigen NY-LU-1; Aldolase; Aldolase
Gene Introduction:
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.