ALDOA antibody can be used for detection of ALDOA by ELISA at 1:62500. ALDOA antibody can be used for detection of ALDOA by western blot at 0.25 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Restrictions
For Research Use only
Format
Lyophilized
Reconstitution
Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.
Concentration
1 mg/mL
Buffer
Antibody is lyophilized in PBS buffer with 2 % sucrose.
Conseil sur la manipulation
As with any antibody avoid repeat freeze-thaw cycles.
Stock
4 °C/-20 °C
Stockage commentaire
For short periods of storage (days) store at 4 °C. For longer periods of storage, store ALDOA antibody at -20 °C.
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
ALDOA is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. 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.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.