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storage temp.
−20°C
Quality Level
General description
- Glutamate and Pyruvate are transformed into Alanine and α-ketoglutarate in the muscle, through the actions of Alanine aminotransferase (AST) and Pyridoxal Phosphate.
- The α-ketoglutarate transforms to Glutamate through the actions of glutamate dehydrogenase with an addition of ammonia. But, in this pathway, the ammonia is excluded from the muscles.
- The Alanine passes through the blood stream and into the liver. In the liver, the Alanine and a-ketoglutarate transform to Pyruvate and Glutamate by the actions of Alanine aminotransferase (AST).
- The Pyruvate transforms to glucose by the Cori cycle (Gluconeogenesis) and returns to the muscle from the blood stream.
Packaging
Each vial is packaged individually and contains 10 mg of the Alanine pathway metabolite standards.
Kit Components Also Available Separately
- A2754Adenosine 5′-diphosphate sodium salt, bacterial, ≥95% (HPLC) 10 mgSDS
- A2252Adenosine 5′-monophosphate monohydrate, from yeast, ≥97% 10 mgSDS
- A2383Adenosine 5′-triphosphate disodium salt hydrate, Grade I, ≥99%, from microbial 10 mgSDS
- B4501Biotin, ≥99% (HPLC), lyophilized powder 10 mgSDS
- G7126Glycine, ReagentPlus®, ≥99% (HPLC) 10 mgSDS
- G10601Glyoxylic acid monohydrate, 98% 10 mgSDS
- A7627L-Alanine, ≥98% (TLC) 10 mgSDS
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Irrit. 2 - Skin Sens. 1
Storage Class Code
8A - Combustible corrosive hazardous materials
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