SKU: WP15134 Categories: ,

Gl Syn Polyclonal Antibody

Price range: $268.00 through $328.00

SKU: WP15134-100
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Product details

Background:

The protein encoded by this gene belongs to the glutamine synthetase family. It catalyzes the synthesis of glutamine from glutamate and ammonia in an ATP-dependent reaction. This protein plays a role in ammonia and glutamate detoxification, acid-base homeostasis, cell signaling, and cell proliferation. Glutamine is an abundant amino acid, and is important to the biosynthesis of several amino acids, pyrimidines, and purines. Mutations in this gene are associated with congenital glutamine deficiency, and overexpression of this gene was observed in some primary liver cancer samples. There are six pseudogenes of this gene found on chromosomes 2, 5, 9, 11, and 12. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014],

Specifications

Size50μL/100μL
TargetGlutamine Synthetase
ReactivityHuman, Mouse, Rat
ApplicationsWB, ELISA
MW(Calculated)
MW(Observed)42kD
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-1:2000; ELISA 1:20000; Not yet tested in other applications.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenThe antiserum was produced against synthesized peptide derived from human Gl Syn. AA range:295-344
SpecificityGl Syn Polyclonal Antibody detects endogenous levels of Gl Syn protein.
Gene NameGLUL
Protein NameGlutamine synthetase
Other NameGLUL; / GLNS; / Glutamine synthetase; / GS; / Glutamate decarboxylase; / Glutamate--ammonia ligase
SpeciesHuman
Gene ID2752
UniprotP15104,
Species.1Mouse
Gene ID.114645
Uniprot.1P15105,
Species.2Rat
Gene ID.224957
Uniprot.2P09606
Cellular LocalizationCytoplasm, cytosol . Microsome . Mitochondrion . Cell membrane; Lipid-anchor . Mainly localizes in the cytosol, with a fraction associated with the cell membrane. .
Tissue ExpressionExpressed in endothelial cells.
Signaling_pathwayCellular Processes >> Cell growth and death >> Necroptosis;Organismal Systems >> Nervous system >> Glutamatergic synapse
Research Areas>>Arginine biosynthesis; / >>Alanine, aspartate and glutamate metabolism; / >>Glyoxylate and dicarboxylate metabolism; / >>Nitrogen metabolism; / >>Metabolic pathways; / >>Biosynthesis of amino acids; / >>Necroptosis; / >>Glutamatergic synapse; / >>GABAergic synapse
FunctionCatalytic activity:ATP + L-glutamate + NH(3) = ADP + phosphate + L-glutamine.,Disease:Defects in GLUL are the cause of congenital systemic glutamine deficiency (CSGD) [MIM:610015]. CSGD is a rare developmental disorder with severe brain malformation resulting in multi-organ failure and neonatal death. Glutamine is largely absent from affected patients serum, urine and cerebrospinal fluid.,online information:Glutamine synthetase entry,similarity:Belongs to the glutamine synthetase family.,subunit:Homooctamer.,
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