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Glutamine Synthetase Monoclonal antibody, PBS Only (Detector)
Glutamine Synthetase Monoclonal Antibody for WB, IHC, IF, Cytometric bead array, Indirect ELISA
Host / Isotype
Mouse / IgG2b
Reactivity
human, pig, zebrafish
Applications
WB, IHC, IF, Cytometric bead array, Indirect ELISA
Conjugate
Unconjugated
CloneNo.
1D10G8
Cat no : 66323-1-PBS
Synonyms
Validation Data Gallery
Tested Applications
Recommended dilution
Application | Dilution |
---|---|
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. |
Product Information
66323-1-PBS targets Glutamine Synthetase as part of a matched antibody pair:
MP50483-1: 66323-2-PBS capture and 66323-1-PBS detection (validated in Cytometric bead array)
Unconjugated mouse monoclonal antibody pair in PBS only (BSA and azide free) storage buffer at a concentration of 1 mg/mL, ready for conjugation.
This conjugation ready format makes antibodies ideal for use in many applications including: ELISAs, multiplex assays requiring matched pairs, mass cytometry, and multiplex imaging applications.Antibody use should be optimized by the end user for each application and assay.
Tested Reactivity | human, pig, zebrafish |
Host / Isotype | Mouse / IgG2b |
Class | Monoclonal |
Type | Antibody |
Immunogen | Glutamine Synthetase fusion protein Ag6309 相同性解析による交差性が予測される生物種 |
Full Name | glutamate-ammonia ligase (glutamine synthetase) |
Calculated molecular weight | 374 aa, 42 kDa |
Observed molecular weight | 42 kDa |
GenBank accession number | BC011700 |
Gene symbol | Glutamine Synthetase |
Gene ID (NCBI) | 2752 |
Conjugate | Unconjugated |
Form | Liquid |
Purification Method | Protein A purification |
Storage Buffer | PBS Only |
Storage Conditions | Store at -80°C. |
Background Information
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).