Full length protein
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in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
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Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Constituents: 10% Glycerol, 20mM Tris HCl, 1mM DTT, pH 8.0
6-bisphosphate 1-phosphohydrolase 1
D fructose 1 6 bisphosphate 1 phosphohydrolase 1
Carbohydrate biosynthesis; gluconeogenesis.
Defects in FBP1 are the cause of fructose-1,6-bisphosphatase deficiency (FBPD) [MIM:229700]. FBPD is inherited as an autosomal recessive disorder mainly in the liver and causes life-threatening episodes of hypoglycemia and metabolic acidosis (lactacidemia) in newborn infants or young children.
Belongs to the FBPase class 1 family.
Information by UniProt
Recombinant Human FBP1 protein 图像
Recombinant Human FBP1 protein (ab89244)参考文献
has not yet been referenced specifically in any publications.
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