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GALE Polyclonal Antibody

Catalog # Availability Size / Price Inquiry
APR26668N-1 50ul / $395
APR26668N-2 100ul / $495
APR26668N-3 200ul / $595

GALE Polyclonal Antibody

Brand

Leading Biology

Catalog Number

APR26668N

Product Type

Polyclonal Antibodies

Field of Research

Endocrine & Metabolism>Carbohydrate metabolism

Product Overview

We constantly strive to ensure we provide our customers with the best antibodies. As a result of this work we offer this antibody in purified format. We are in the process of updating our datasheets. If you have any questions regarding this update, please feel free to contact our technical support team. This product is a high quality GALE Polyclonal Antibody.

Molecular Weight

Calculated MW: 30kDa/38kDa Observed MW: 38kDa

Species Reactivity

Rabbit

Immunogen

Recombinant fusion protein of human GALE (NP_001121093.1).

Cross Reactivity

Human,Mouse,Rat

Isotype

IgG

GeneID

UniProt ID

Purity

Affinity purification

Storage & Stability

Store at +4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

Storage Buffer

Buffer: PBS with 50% glycerol, pH7.3.

Applications

WB,IHC,IF

Dilution

WB 1:500 - 1:2000 IHC 1:50 - 1:200 IF 1:10 - 1:100

Product Description

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.

Synonyms

GALE; SDR1E1; UDP-glucose 4-epimerase

Images

Western blot analysis of extracts of various cell lines, using GALE antibody.

Immunofluorescence analysis of A549 cells using GALE antibody.

Specification

Quantity

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