• Phare
  • Validé par KD/KO

Anticorps Monoclonal anti-Glutamine Synthetase

Glutamine Synthetase Monoclonal Antibody for IF-P

Hôte / Isotype

Mouse / IgG1

Réactivité testée

Humain, rat, souris

Applications

IF-P

Conjugaison

CoraLite® Plus 488 Fluorescent Dye

CloneNo.

1B6G4

N° de cat : CL488-66323-2

Synonymes

GLUL, 1B6G4, EC:2.3.1.225, EC:6.3.1.2, GLNS



Applications testées

Résultats positifs en IF-Ptissu cérébral de souris,

Dilution recommandée

ApplicationDilution
Immunofluorescence (IF)-PIF-P : 1:50-1:500
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, check data in validation data gallery

Informations sur le produit

CL488-66323-2 cible Glutamine Synthetase dans les applications de IF-P et montre une réactivité avec des échantillons Humain, rat, souris

Réactivité Humain, rat, souris
Hôte / Isotype Mouse / IgG1
Clonalité Monoclonal
Type Anticorps
Immunogène Glutamine Synthetase Protéine recombinante Ag6309
Nom complet glutamate-ammonia ligase (glutamine synthetase)
Masse moléculaire calculée 374 aa, 42 kDa
Poids moléculaire observé42 kDa
Numéro d’acquisition GenBankBC011700
Symbole du gène Glutamine Synthetase
Identification du gène (NCBI) 2752
Conjugaison CoraLite® Plus 488 Fluorescent Dye
Excitation/Emission maxima wavelengths493 nm / 522 nm
Forme Liquide
Méthode de purification Purification par protéine G
Tampon de stockage PBS with 50% glycerol, 0.05% Proclin300, 0.5% BSA
Conditions de stockageStocker à -20 °C. Éviter toute exposition à la lumière. Stable pendant un an après l'expédition. L'aliquotage n'est pas nécessaire pour le stockage à -20oC Les 20ul contiennent 0,1% de BSA.

Informations générales

GLUL(Glutamine synthetase) is also named as GS,GLNS and belongs to the glutamine synthetase family.This enzyme has 2 functions: it catalyzes the production of glutamine and 4-aminobutanoate (gamma-aminobutyric acid, GABA), the latter in a pyridoxal phosphate-independent manner By similarity. Essential for proliferation of fetal skin fibroblasts (PMID:18662667).Defects in GLUL are the cause of congenital systemic glutamine deficiency (CSGD).Organismal glutamine production is augmented secondary to an increase in the activity of glutamine synthetase in the lung and skeletal muscle(PMID:7630137). There are other bands with higher (66 kDa, 97 kDa) and lower (30 kDa)molecular weights also detected besides the 42 kDa band indicating the proteolysis of GLUL protein by the ubiquitin system(PMID:10091759).

Protocole

Product Specific Protocols
IF protocol for CL Plus 488 Glutamine Synthetase antibody CL488-66323-2Download protocol
Standard Protocols
Click here to view our Standard Protocols

Avis

The reviews below have been submitted by verified Proteintech customers who received an incentive for providing their feedback.


FH

Jaide (Verified Customer) (04-07-2025)

Only GLUL antibody I have test that is specific to central veins in mouse liver. It created clear precise staining that is easy to optimize.

  • Applications: Immunofluorescence
  • Primary Antibody Dilution: 1:50
  • Cell Tissue Type: Mouse Liver/ Central Veins
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