GBE1 Mouse Monoclonal Antibody [Clone ID: LBI4D9]

Product Specifications

Background

The protein encoded by this gene is a glycogen branching enzyme that catalyzes the transfer of alpha-1,4-linked glucosyl units from the outer end of a glycogen chain to an alpha-1,6 position on the same or a neighboring glycogen chain. Branching of the chains is essential to increase the solubility of the glycogen molecule and, consequently, in reducing the osmotic pressure within cells. Highest level of this enzyme are found in liver and muscle. Mutations in this gene are associated with glycogen storage disease IV (also known as Andersen's disease) . [provided by RefSeq]

Overview

GBE1 mouse monoclonal antibody, clone LBI4D9

Synonyms

APBD; GBE; GSD4

Gene Name

1,4-alpha-glucan branching enzyme 1

Gene ID

2632

UniProt

Q04446

Conjugation

Unconjugated

Related Pathways

Metabolic pathways, Starch and sucrose metabolism

Field of Research

Metabolic pathways, Starch and sucrose metabolism

Concentration

0.7 mg/ml

Dilution

WB 1:2000, IF 1:100, FLOW 1:100, IP 2ug/500ul

Form

PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

Buffer

PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

Function

Druggable Genome

Storage Conditions

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.