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.
Beschränkungen
Nur für Forschungszwecke einsetzbar
Format
Lyophilized
Rekonstitution
Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.
Konzentration
1 mg/mL
Buffer
Antibody is lyophilized in PBS buffer with 2 % sucrose.
Handhabung
As with any antibody avoid repeat freeze-thaw cycles.
Lagerung
4 °C/-20 °C
Informationen zur Lagerung
For short periods of storage (days) store at 4 °C. For longer periods of storage, store ALDOA antibody at -20 °C.
ALDA antikoerper, GSD12 antikoerper, aldoa antikoerper, cb79 antikoerper, sb:cb79 antikoerper, wu:fa28b10 antikoerper, wu:fb10b11 antikoerper, ALDOA antikoerper, Aldo-1 antikoerper, Aldo1 antikoerper, RNALDOG5 antikoerper, hm:zeh0036 antikoerper, zgc:77696 antikoerper, aldolase, fructose-bisphosphate A antikoerper, aldolase a, fructose-bisphosphate, a antikoerper, aldolase, fructose-bisphosphate A S homeolog antikoerper, aldolase A, fructose-bisphosphate antikoerper, aldolase a, fructose-bisphosphate, b antikoerper, ALDOA antikoerper, aldoaa antikoerper, aldoa antikoerper, aldoa.S antikoerper, Aldoa antikoerper, aldoab antikoerper
Hintergrund
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.