Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
Homologie
Rb
Purification
This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.
Immunogène
This ALDOA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 303-331 amino acids from the C-terminal region of human ALDOA.
anticorps ALDA, anticorps GSD12, anticorps aldoa, anticorps cb79, anticorps sb:cb79, anticorps wu:fa28b10, anticorps wu:fb10b11, anticorps ALDOA, anticorps Aldo-1, anticorps Aldo1, anticorps RNALDOG5, anticorps hm:zeh0036, anticorps zgc:77696, anticorps aldolase, fructose-bisphosphate A, anticorps aldolase a, fructose-bisphosphate, a, anticorps aldolase, fructose-bisphosphate A S homeolog, anticorps aldolase A, fructose-bisphosphate, anticorps aldolase a, fructose-bisphosphate, b, anticorps ALDOA, anticorps aldoaa, anticorps aldoa, anticorps aldoa.S, anticorps Aldoa, anticorps aldoab
Sujet
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.