- 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
Galerie de données de validation
Applications testées
Résultats positifs en IF-P | tissu cérébral de souris, |
Dilution recommandée
Application | Dilution |
---|---|
Immunofluorescence (IF)-P | IF-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 observé | 42 kDa |
Numéro d’acquisition GenBank | BC011700 |
Symbole du gène | Glutamine Synthetase |
Identification du gène (NCBI) | 2752 |
Conjugaison | CoraLite® Plus 488 Fluorescent Dye |
Excitation/Emission maxima wavelengths | 493 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 stockage | Stocker 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 | |
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IF protocol for CL Plus 488 Glutamine Synthetase antibody CL488-66323-2 | Download protocol |
Standard Protocols | |
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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.
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