GBE1 Mouse Monoclonal Antibody [Kloon ID: LBI4D9]

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]

Carrier-free (BSA/glycerol-free) GBE1 mouse monoclonal antibody, clone LBI4D9

APBD; GBE; GSD4

Homo sapiens 1,4-alpha-glucan branching enzyme 1 (GBE1), mRNA.

2632

Q04446

Unconjugated

Metabolic pathways, Starch and sucrose metabolism

Metabolic pathways, Starch and sucrose metabolism

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

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Druggable Genome

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable 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.

GBE1

https://www.ncbi.nlm.nih.gov/gene/?term=2632

https://www.uniprot.org/uniprot/Q04446