E-AB-10125
ALDOA Polyclonal Antibody
Size
£106.20
Was £118.00
- SKU:
- E-AB-10125
- Additional Names:
- ALDA,ALDOA,Aldo1,Aldolase,Aldolase 1,Aldolase A,Aldolase A fructose bisphosphatase,Aldolase A fructose bisphosphate,Epididymis secretory sperm binding protein Li 87p,FRUCTOALDOLASE A,Fructose 1 6 bisphosphate triosephosphate ,fructose-bisphosphate A
- Application:
- IHC, WB
- Concentration:
- 0.3 mg/ml
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Avoid freeze/thaw cycles.
- Supplier:
- Elabscience
- Host:
- Rabbit
- Reactivities:
- Human, Mouse, Rat
- Buffer:
- Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
- Immunogen:
- Recombinant protein of human ALDOA
- Uniprot:
- P04075
- Synonyms:
- ALDA;aldolase A, fructose-bisphosphate;epididymis secretory sperm binding protein Li 87p;fructose-1,6-bisphosphate triosephosphate-lyase;fructose-bisphosphate aldolase A;GSD12;HEL-S-87p;lung cancer antigen NY-LU-1;muscle-type aldolase
- Extra Details:
- The protein encoded by this gene, 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 and alternative promoter usage results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 3 and 10.
- Shipping Conditions:
- Blue Ice