Glutamine Synthetase (GLUL) Mouse Monoclonal Antibody [Kloon ID: LBI1F4]

The protein encoded by this gene belongs to the glutamine synthetase family. It catalyzes the synthesis of glutamine from glutamate and ammonia. Glutamine is a main source of energy and is involved in cell proliferation, inhibition of apoptosis, and cell signaling. This gene is expressed during early fetal stages, and plays an important role in controlling body pH by removing ammonia from circulation. Mutations in this gene are associated with congenital glutamine deficiency. Several alternatively spliced transcript variants have been found for this gene.

Carrier-free (BSA/glycerol-free) GLUL mouse monoclonal antibody, clone LBI1F4

GLNS; GS; PIG43; PIG59

Homo sapiens glutamate-ammonia ligase (GLUL), transcript variant 1, mRNA.

2752

P15104

Unconjugated

Alanine, aspartate and glutamate metabolism, Arginine and proline metabolism, Metabolic pathways, Nitrogen metabolism

Alanine, aspartate and glutamate metabolism, Arginine and proline metabolism, Metabolic pathways, Nitrogen metabolism

WB 1:1000~2000, IHC 1:50, IF 1:50~100, FLOW 1:100

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

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

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.

GLUL

https://www.ncbi.nlm.nih.gov/gene/?term=2752

https://www.uniprot.org/uniprot/P15104