Product overview:

Carrier-free (BSA/glycerol-free) GBE1 mouse monoclonal antibody, clone LBI5B7

Field of research:

Metabolic pathways, Starch and sucrose metabolism

Summary:

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]

Alternative names:

APBD; GBE; GSD4

Species reactivity:

Human, Mouse, Rat

Host:

Mouse

Target:

GBE1

Isotype:

IgG1

Immunogen:

Full length human recombinant protein of human GBE1 (NP_000149) produced in HEK293T cell.

Clone:

LBI5B7

Conjugation:

Unconjugated

Gene name:

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

Symbol:

GBE1

Pathway:

Metabolic pathways, Starch and sucrose metabolism

Function:

Druggable Genome

Purification:

Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)

Concentration:

Form:

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

Applications & dilution:

WB 1:2000, IHC 1:50, FLOW 1:100, IP 2ug/500ul

Storage buffer:

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

Storage:

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.

More info:

Email: info@sobekbio.com

Orders:

Email: orders@sobekbio.com