Anti-Glutamine synthetase antibody [HL2283]
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Rabbit Monoclonal Glutamine Synthetase antibody. Suitable for WB, IHC-P and reacts with Transfected cell lysate, Human, Mouse, Rat, Dog, Cat samples. Immunogen corresponding to Recombinant Full Length Protein corresponding to Human GLUL.
View Alternative Names
GLNS, GLUL, Glutamine synthetase, GS, Glutamate--ammonia ligase, Palmitoyltransferase GLUL
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glutamine synthetase antibody [HL2283] (AB317188)
ab317188 detects Glutamine synthetase protein by immunohistochemical analysis. Sample : Paraffin-embedded rat tissues. Glutamine synthetase stained by ab317188 diluted at 1 : 100. Antigen Retrieval : Citrate buffer pH 6.0 15 min.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glutamine synthetase antibody [HL2283] (AB317188)
ab317188 detects Glutamine synthetase protein by immunohistochemical analysis. Sample : Paraffin-embedded mouse tissues. Glutamine synthetase stained by ab317188 diluted at 1 : 100. Antigen Retrieval : Citrate buffer pH 6.0 15 min.
- WB
Supplier Data
Western blot - Anti-Glutamine synthetase antibody [HL2283] (AB317188)
Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE and the membrane was blotted with ab317188 diluted at 1 : 2000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody. Corresponding RNA expression data for the same cell lines are based on Human Protein Atlas program.
All lanes:
Western blot - Anti-Glutamine synthetase antibody [HL2283] (ab317188) at 1/2000 dilution
Lane 1:
HeLa whole cell extracts at 30 µg
Lane 2:
SK-MEL-28 whole cell extracts at 30 µg
Secondary
All lanes:
HRP-conjugated anti-rabbit IgG antibody
false
- WB
Supplier Data
Western blot - Anti-Glutamine synthetase antibody [HL2283] (AB317188)
Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE and the membrane was blotted with ab317188 diluted at 1 : 5000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
All lanes:
Western blot - Anti-Glutamine synthetase antibody [HL2283] (ab317188) at 1/5000 dilution
Lane 1:
Non-transfected (-) 293T whole cell extracts at 30 µg
Lane 2:
GLUL shRNA transfected (+) 293T whole cell extracts at 30 µg
Secondary
All lanes:
HRP-conjugated anti-rabbit IgG antibody
false
- WB
Supplier Data
Western blot - Anti-Glutamine synthetase antibody [HL2283] (AB317188)
Various tissue extracts (50 ug) were separated by 10% SDS-PAGE and the membrane was blotted with ab317188 diluted at 1 : 5000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
All lanes:
Western blot - Anti-Glutamine synthetase antibody [HL2283] (ab317188) at 1/5000 dilution
Lane 1:
Mouse brain tissue extract at 50 µg
Lane 2:
Rat brain tissue extract at 50 µg
Secondary
All lanes:
HRP-conjugated anti-rabbit IgG antibody
false
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glutamine synthetase antibody [HL2283] (AB317188)
ab317188 detects Glutamine synthetase protein at cell membrane and cytoplasm by immunohistochemical analysis. Sample : Paraffin-embedded cat cerebellum. Glutamine synthetase stained by ab317188 diluted at 1 : 100. Antigen Retrieval : Citrate buffer pH 6.0 15 min.
- WB
Supplier Data
Western blot - Anti-Glutamine synthetase antibody [HL2283] (AB317188)
Whole cell extract (30 ug) was separated by 10% SDS-PAGE and the membrane was blotted with ab317188 diluted at 1 : 1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
All lanes:
Western blot - Anti-Glutamine synthetase antibody [HL2283] (ab317188) at 1/1000 dilution
All lanes:
MDCK whole cell extract at 30 µg
Secondary
All lanes:
HRP-conjugated anti-rabbit IgG antibody
false
- WB
Supplier Data
Western blot - Anti-Glutamine synthetase antibody [HL2283] (AB317188)
Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE and the membrane was blotted with ab317188 diluted at 1 : 5000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
All lanes:
Western blot - Anti-Glutamine synthetase antibody [HL2283] (ab317188) at 1/5000 dilution
Lane 1:
Non-transfected (-) 293T whole cell extracts at 30 µg
Lane 2:
DDDDK-tagged GLUL transfected (+) 293T whole cell extracts at 30 µg
Secondary
All lanes:
HRP-conjugated anti-rabbit IgG antibody
false
Reactivity data
Properties and storage information
Form
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Glutamate-ammonia ligase performs an important function in nitrogen metabolism by catalyzing the reaction that produces glutamine a vital amino acid and a source of cellular carbon and nitrogen. This enzyme also participates in the detoxification of ammonia a process critical in the brain. It is known to operate as part of a larger enzyme complex working intricately with other cellular components to maintain nitrogen balance and detoxify harmful metabolic byproducts.
Pathways
The glutamate-ammonia ligase enzyme plays an integral role in the urea cycle and the glutamine-glutamate cycle. The urea cycle is pivotal in converting potentially harmful ammonia to urea for safe excretion showing close interaction with carbamoyl phosphate synthetase. In the glutamine-glutamate cycle the enzyme assists in neurotransmitter cycling and nitrogen metabolism interacting with proteins like glutaminase which converts glutamine back to glutamate.
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Target data
Product promise
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