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GALE Mouse anti-Canine, Human, Rat, Clone: OTI1C4, lyophilized, TrueMAB™
SDP

Mouse Monoclonal Antibody

Supplier:  OriGene CF502146

Encompass_Preferred

Catalog No. 50-166-1078


May include imposed supplier surcharges.
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Description

Description

Reconstitute with PBS (pH 7.3) and recommend to perform another round of desalting process using Product No. 7KMWCO

This gene encodes UDP-galactose-4-epimerase which catalyzes two distinct but analogous reactions: the epimerization of UDP-glucose to UDP-galactose, and the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine. The bifunctional nature of the enzyme has the important metabolic consequence that mutant cells (or individuals) are dependent not only on exogenous galactose, but also on exogenous N-acetylgalactosamine as a necessary precursor for the synthesis of glycoproteins and glycolipids. Mutations in this gene result in epimerase-deficiency galactosemia, also referred to as galactosemia type 3, a disease characterized by liver damage, early-onset cataracts, deafness and mental retardation, with symptoms ranging from mild (′peripheral′ form) to severe (′generalized′ form). Multiple alternatively spliced transcripts encoding the same protein have been identified.
Specifications

Specifications

GALE
Monoclonal
Unconjugated
GALE
SDR1E1
Mouse
Affinity Chromatography
RUO
100855555, 114860, 2582
-20° C, Avoid Freeze/Thaw Cycles
Lyophilized
Immunohistochemistry (Paraffin), Western Blot
OTI1C4
PBS with 8% trehalose and no preservative; pH 7.3
P18645, Q14376
GALE
Full length human recombit protein of human GALE produced in HEK293T cell.
100 μg
Primary
Canine, Human, Rat
Antibody
IgG1
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