BD-PT0192

Aldolase B Rabbit Polyclonal Antibody

ALDOB; ALDB; Fructose-bisphosphate aldolase B; Liver-type aldolase

常规抗体

ALDOB

Fructose-bisphosphate aldolase B

WB

Human,Mouse,Rat

1 mg/ml

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.

229

http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=229

P05062

http://www.uniprot.org/uniprotkb/P05062/entry

230163

http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=230163

Q91Y97

http://www.uniprot.org/uniprot/Q91Y97

P00884

http://www.uniprot.org/uniprot/P00884

The antiserum was produced against synthesized peptide derived from human ALDOB. AA range:111-160

Aldolase B Polyclonal Antibody detects endogenous levels of Aldolase B protein.

WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:20000.. IF 1:50-200

39kD

-20°C/1 year

Polyclonal, Rabbit,IgG

Fructose-1,6-bisphosphate aldolase (EC 4.1.2.13) is a tetrameric glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Vertebrates have 3 aldolase isozymes which are distinguished by their electrophoretic and catalytic properties. Differences indicate that aldolases A, B, and C are distinct proteins, the products of a family of related 'housekeeping' genes exhibiting developmentally regulated expression of the different isozymes. The developing embryo produces aldolase A, which is produced in even greater amounts in adult muscle where it can be as much as 5% of total cellular protein. In adult liver, kidney and intestine, aldolase A expression is repressed and aldolase B is produced. In brain and other nervous tissue, aldolase A and C are expressed about equally. There is a high

Kidney,

Cytoplasm, cytoskeleton, microtubule organizing center, centrosome, centriolar satellite .

Glycolysis / Gluconeogenesis;Pentose phosphate pathway;Fructose and mannose metabolism;

catalytic activity:D-fructose 1,6-bisphosphate = glycerone phosphate + D-glyceraldehyde 3-phosphate.,disease:Defects in ALDOB are the cause of hereditary fructose intolerance (HFI) [MIM:229600]. HFI is an autosomal recessive disease that results in an inability to metabolize fructose and related sugars. Complete exclusion of fructose results in dramatic recovery; however, if not treated properly, HFI subjects suffer episodes of hypoglycemia, general ill condition, and risk of death the remainder of life.,miscellaneous:In vertebrates, three forms of this ubiquitous glycolytic enzyme are found, aldolase A in muscle, aldolase B in liver and aldolase C in brain.,pathway:Carbohydrate degradation; glycolysis; D-glyceraldehyde 3-phosphate and glycerone phosphate from D-glucose: step 4.,pathway:Carbohydrate degradation; glycolysis; D-glyceraldehyde 3-phosphate and glycerone phosphate from D-glucose: step 4/4.,similarity:Belongs to the class I fructose-bisphosphate aldolase family.,subunit:Homotetramer.,

现货

The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.