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Rabbit Polyclonal Glutamine antibody. Suitable for ICC, IHC-FoFr, IM, IHC-Fr and reacts with Modified Amino Acid samples. Cited in 5 publications. Immunogen corresponding to Chemical / Small Molecule corresponding to Glutamine.

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Publications

Key facts

Isotype
IgG
Host species
Rabbit
Storage buffer
Standard buffer
Form
Liquid
Clonality
Polyclonal

Immunogen

  • Chemical / Small Molecule corresponding to Glutamine.

Reactivity data

Select an application
Product promiseTestedExpectedPredictedNot recommended
ICCIHC-FoFrIMIHC-Fr
Modified Amino Acid
Expected
Expected
Expected
Expected

Expected
Expected

Species
Modified Amino Acid
Dilution info
Use at an assay dependent concentration.
Notes

-

Expected
Expected

Species
Modified Amino Acid
Dilution info
Use at an assay dependent concentration.
Notes

-

Expected
Expected

Species
Modified Amino Acid
Dilution info
Use at an assay dependent concentration.
Notes

-

Expected
Expected

Species
Modified Amino Acid
Dilution info
Use at an assay dependent concentration.
Notes

-

Alternative names

Recommended products

Rabbit Polyclonal Glutamine antibody. Suitable for ICC, IHC-FoFr, IM, IHC-Fr and reacts with Modified Amino Acid samples. Cited in 5 publications. Immunogen corresponding to Chemical / Small Molecule corresponding to Glutamine.

Key facts

Isotype
IgG
Form
Liquid
Clonality
Polyclonal
Immunogen
  • Chemical / Small Molecule corresponding to Glutamine.
Purity
IgG fraction
Specificity

The antibody is calibrated against a spectrum of antigens to assure hapten selectivity. No measurable cross-reactivity (<1:1000) was detected against glutamine in peptides or proteins. Fixed tissue cross-reactivity was tested with known targets at the recommended dilution. No measurable glutaraldehyde-fixed tissue cross-reactivity (<1:1000) was detected against L-alanine, gamma-aminobutyrate, agmatine, guanidine, D/L-arginine, L-citrulline, L-cysteine, D/L-glutamate, glutathione, glycine, L-lysine, L-ornithine, L-serine, taurine, L-threonine, L-tryptophan, L-tyrosine.

Concentration
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Storage

Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Storage information
Avoid freeze / thaw cycle

Supplementary info

This supplementary information is collated from multiple sources and compiled automatically.
Activity summary

Glutamine often abbreviated as Gln is an amino acid with a molecular weight of approximately 146.15 g/mol. It serves as a significant nitrogen donor in cellular processes and contributes to synthesizing nucleotides and amino acids. The amino acid is non-essential meaning the body can synthesize it as needed mainly produced in muscles and distributed via the bloodstream to other tissues including the liver brain and immune cells. Glutamine's role in ammonia transportation is notable as it helps in detoxifying ammonium ions. It influences cellular proliferation through its involvement in various cellular functions.

Biological function summary

Glutamine plays an important role in supporting rapid cell division and growth such as in the immune system and intestinal tract. It forms part of the larger metabolic function known as glutaminolysis which provides energy and precursors for biosynthesis. Within cells glutamine works in tandem with several enzymes and transport proteins such as glutamine synthetase which regulates its production and use. The connection with the liver is significant as the organ converts glutamine into glucose and ammonium with glutamate acting as an intermediary.

Pathways

The role of glutamine extends to important areas like the tricarboxylic acid (TCA) cycle and the glutamate-glutamine cycle. In the TCA cycle it serves as a carbon source feeding into gluconeogenesis and other biosynthetic pathways. The conversion to glutamate followed by other downstream metabolites links glutamine closely to amino acid metabolism. Important proteins like glutamate dehydrogenase facilitate these conversions and highlight the interconnected nature of these metabolic pathways.

Associated diseases and disorders

Abnormalities in glutamine metabolism have associations with conditions such as cancer and neurodegenerative diseases. Cancer cells often exhibit increased glutamine uptake supporting their rapid growth through metabolic pathways like glutaminolysis. On the other hand neurodegenerative diseases involve disruptions in the glutamate-glutamine cycle implicating excitotoxicity-related proteins like NMDA receptors. Altered levels of glutamine and associated proteins in these diseases suggest potential therapeutic targets and diagnostic markers emphasizing its role in cellular health and disease progression.

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