Glutamine Synthetase Rabbit pAb

-YT5035

Catalog: YT5035
Size
Price
Status
Qty.
200μL
$450.00
4 weeks

0

100μL
$280.00
4 weeks

0

40μL
$150.00
4 weeks

0

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Collected

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Main Information
Target

Glutamine synthetase

Host Species

Rabbit

Reactivity

Human, Mouse, Rat

Applications

WB, ELISA

MW

42kD (Observed)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
WB 1:500-1:2000; ELISA 1:20000; Not yet tested in other applications.
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Specificity
Gl Syn Polyclonal Antibody detects endogenous levels of Gl Syn protein.
Purification
The 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)
Concentration
1 mg/ml
MW(Observed)
42kD
Modification
Unmodified
Clonality
Polyclonal
Isotype
IgG
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Antigen&Target Information
Immunogen:
The antiserum was produced against synthesized peptide derived from human Gl Syn. AA range:295-344
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Specificity:
Gl Syn Polyclonal Antibody detects endogenous levels of Gl Syn protein.
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Gene Name:
GLUL
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Protein Name:
Glutamine synthetase
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Other Name:
GLUL ;
GLNS ;
Glutamine synthetase ;
GS ;
Glutamate decarboxylase ;
Glutamate--ammonia ligase
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Database Link:
Organism Gene ID SwissProt
Human 2752; P15104;
Mouse 14645; P15105;
Rat 24957; P09606;
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] ,
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Function:
Catalytic 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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Cellular Localization:
Cytoplasm , cytosol . Microsome . Mitochondrion . Cell membrane ; Lipid-anchor . Mainly localizes in the cytosol , with a fraction associated with the cell membrane. .
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Tissue Expression:
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
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Catalog: YT5035
Size
Price
Status
Qty.
200μL
$450.00
4 weeks

0

100μL
$280.00
4 weeks

0

40μL
$150.00
4 weeks

0

Add to cart

Collected

Collect

Customized Service

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