Promotion ends on May 1st.
Also for GALT (NM_000155)
|Expression cDNA Clone or AA Sequence
Recombinant protein was produced with TrueORF clone, RC202206
. Click on the TrueORF clone link to view cDNA and protein sequences.
||Predicted MW:||43.2 kDa|
|Purity:||> 80% as determined by SDS-PAGE and Coomassie blue staining|
|Mass Spec Validation:
||This protein has been positively validated by MS/MS by Dr. Robert Moritz at The Institute of Systems Biology.
|Concentration:||>50 ug/mL as determined by microplate BCA method|
|Buffer:||25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol.|
||Recombinant protein was captured through anti-DDK affinity column followed by conventional chromatography steps.
||Galactose metabolismAmino sugar and nucleotide sugar metabolismMetabolic pathways
||RefSeq Size: 1347
||RefSeq ORF: 1140|
|Synonyms : OTTHUMP00000021298; galactose-1-phosphate uridyl transferase; galactose-1-phosphate uridylyltransferase|
|Summary: 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]. |
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for specific inventory information
**: DDK-tag is the same as FLAG tag. Flag® is a registered trademark of Sigma-Aldrich