GeneBio Systems
Anti-Glutaminase/GLS Antibody Picoband® (monoclonal, 3G13)
Anti-Glutaminase/GLS Antibody Picoband® (monoclonal, 3G13)
SKU:M01272-3
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Size: 100 μg
Storage: At -20℃ for one year from date of receipt. After reconstitution, at 4℃ for one month. It can also be aliquotted and stored frozen at -20℃ for six months. Avoid repeated freezing and thawing.
Form: Lyophilized
Reactivity: Human,Mouse,Rat
Applications: WB,IHC,ICC,IF,Flow Cytometry
Application Details: Western blot, 0.25-0.5 μg/ml, Human, Mouse, Rat
Immunohistochemistry(Paraffin-embedded Section), 2-5 μg/ml, Human
Immunocytochemistry/Immunofluorescence, 5 μg/ml, Human
Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
Gene Name: GLS
Specificity:
Background: This gene encodes the K-type mitochondrial glutaminase. The encoded protein is an phosphate-activated amidohydrolase that catalyzes the hydrolysis of glutamine to glutamate and ammonia. This protein is primarily expressed in the brain and kidney plays an essential role in generating energy for metabolism, synthesizing the brain neurotransmitter glutamate and maintaining acid-base balance in the kidney. Alternate splicing results in multiple transcript variants.
Immunogen: E.coli-derived human Glutaminase/GLS recombinant protein (Position: K396-N654).
Clonality: Monoclonal
Contents: Each vial contains 4 mg Trehalose, 0.9 mg NaCl and 0.2 mg Na2HPO4.
Purification: Immunogen affinity purified.
Reconstitution: Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.
Reference: 1. Lynch, D. S., Chelban, V., Vandrovcova, J., Pittman, A., Wood, N. W., Houlden, H. GLS loss of function causes autosomal recessive spastic ataxia and optic atrophy. Ann. Clin. Transl. Neurol. 5: 216-221, 2018. 2. Modi, W. S., Pollock, D. D., Mock, B. A., Banner, C., Renauld, J.-C., Van Snick, J. Regional localization of the human glutaminase (GLS) and interleukin-9 (IL9) genes by in situ hybridization. Cytogenet. Cell Genet. 57: 114-116, 1991. 3. Rumping, L., Tessadori, F., Pouwels, P. J. W., Vringer, E., Wijnen, J. P., Bhogal, A. A., Savelberg, S. M. C., Duran, K. J., Bakkers, M. J. G., Ramos, R. J. J., Schellekens, P. A. W., Kroes, H. Y., and 16 others. GLS hyperactivity causes glutamate excess, infantile cataract and profound developmental delay. Hum. Molec. Genet. 28: 96-104, 2019.
Uniprot ID: O94925
Host: Mouse
Concentration: Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.
Conjugate:
Cross Reactivity: No cross-reactivity with other proteins.
Isotype: Mouse IgG2a
Phospho_site:
Clone Number: Clone: 3G13
Observed Molecular Weight: 56-73 kDa
Calculated Molecular Weight:
Gene ID: 2744
Protein Name: Glutaminase kidney isoform, mitochondrial
Gene Full Name: glutaminase
Synonyms: AAD20; GAC; GLS; GLS1; glutaminase; K glutaminase; KGA; KGA/GAC; KIAA0838; L glutamine amidohydrolase
