Human Galactose-1-Phosphate Uridylyltransferase (GALT) ELISA Kit | GALT elisa kit
Human Galactose-1-Phosphate Uridylyltransferase (GALT) ELISA Kit
Principle of the Assay: The microtiter plate provided in this kit has been pre-coated with an antibody specific to G6PC. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific to G6PC. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain G6PC, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm +/- 10nm. The concentration of G6PC in the samples is then determined by comparing the O.D. of the samples to the standard curve.
NCBI and Uniprot Product Information
NCBI Description
Galactose-1-phosphate uridyl transferase (GALT) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP-glucose + galactose-1-phosphate to glucose-1-phosphate + UDP-galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]
Uniprot Description
GALT: Defects in GALT are the cause of galactosemia (GALCT). Galactosemia is an inherited disorder of galactose metabolism that causes jaundice, cataracts, and mental retardation. Belongs to the galactose-1-phosphate uridylyltransferase type 1 family.
Protein type: Carbohydrate Metabolism - amino sugar and nucleotide sugar; Carbohydrate Metabolism - galactose; EC 2.7.7.12; Motility/polarity/chemotaxis; Transferase
Chromosomal Location of Human Ortholog: 9p13.3
Cellular Component: cytosol; Golgi apparatus
Molecular Function: protein binding; UDP-glucose:hexose-1-phosphate uridylyltransferase activity; zinc ion binding
Biological Process: galactose catabolic process; galactose catabolic process via UDP-galactose; galactose metabolic process; UDP-glucose catabolic process; UDP-glucose metabolic process
Disease: Galactosemia
Research Articles on GALT
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Product Notes
The Human GALT galt (Catalog #AAA456863) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA456863 ELISA Kit recognizes Human GALT. It is sometimes possible for the material contained within the vial of "Galactose-1-Phosphate Uridylyltransferase (GALT), ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.Precautions
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