Skip to main content

GPT Products

GPT, also known as Alanine aminotransferase 1, is a 496 amino acid that is 55 kDa, cytoplasm located, most commonly found in liver, kidney, heart, and skeletal muscles; acts as a catalyzer of the reversible transamination between alanine and 2-oxoglutarate to compose pyruvate and glutamate, is involved in cellular nitrogen metabolism, and also in liver gluconeogenesis starting with precursors transported from skeletal muscles. Current research is being performed on several diseases and disorders including vitelliform macular dystrophy, liver disease, epidemic typhus, pyomyositis, kidney cortex necrosis, scrub typhus, hepatitis e, hepatitis c, iron overload hepatitis b, glucose intolerance, biliary atresia, alcohol abuse, cholangitis, cholecystitis, hellp syndrome, viral hepatitis, siderosis, choledocholithiasis, hepatitis a, kawasaki disease, wilson disease, and hepatic encephalopathy. This protein has shown to have interactions with CAPN1, CAPN3, HSPD1, THNSL2, GPT2, AND PSAT1 in pathways such as alanine, aspartate and glutamate metabolism, amino acid synthesis and interconversion (transamination), and metabolism of amino acids and derivatives.
Show More

23 results for "GPT" in Products

23 results for "GPT" in Products

GPT Products

GPT, also known as Alanine aminotransferase 1, is a 496 amino acid that is 55 kDa, cytoplasm located, most commonly found in liver, kidney, heart, and skeletal muscles; acts as a catalyzer of the reversible transamination between alanine and 2-oxoglutarate to compose pyruvate and glutamate, is involved in cellular nitrogen metabolism, and also in liver gluconeogenesis starting with precursors transported from skeletal muscles. Current research is being performed on several diseases and disorders including vitelliform macular dystrophy, liver disease, epidemic typhus, pyomyositis, kidney cortex necrosis, scrub typhus, hepatitis e, hepatitis c, iron overload hepatitis b, glucose intolerance, biliary atresia, alcohol abuse, cholangitis, cholecystitis, hellp syndrome, viral hepatitis, siderosis, choledocholithiasis, hepatitis a, kawasaki disease, wilson disease, and hepatic encephalopathy. This protein has shown to have interactions with CAPN1, CAPN3, HSPD1, THNSL2, GPT2, AND PSAT1 in pathways such as alanine, aspartate and glutamate metabolism, amino acid synthesis and interconversion (transamination), and metabolism of amino acids and derivatives.
Show More
Applications: IHC, WB
Reactivity: Human, Mouse, Rat
Applications: Func
Applications: IHC
Reactivity: Human
Applications: ELISA
Applications: IHC, WB
Reactivity: Human, Rat
Applications: IHC, WB
Reactivity: Human
Applications: PAGE, Enzyme Activity
Applications: WB, ELISA
Reactivity: Human
Applications: WB
Reactivity: Human, Mouse
Applications: WB
Reactivity: Human, Mouse
Applications: WB, ELISA
Reactivity: Human, Mouse, Rat
Applications: AC
Applications: WB
Applications: PAGE, Enzyme Activity
Applications: ELISA
Applications: PAGE, Enzyme Activity
Applications: Func
Applications: WB, ELISA
Reactivity: Porcine
Applications: ELISA
Reactivity: Human
Applications: PAGE
Applications: Func
Applications: AC
Catalog #: NBP2-62474
Applications: Bioactivity
Results Per Page
5 10 25 50
/ 1