Aspartate Aminotransferase (AST, GOT), Human Liver

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SKU:
P1299-100
€185
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Description

Aspartate Aminotransferase (AST, GOT), Human Liver is available at Gentaur for Next week delivery.

Biomarkers for liver health.

Biomolecule/Target: Aspartate Aminotransferase (AST, GOT)

Alternates names: Aspartate Transaminase, Glutamate Oxaloacetate, AST, GOT, sGOT, AspAT, ASAT, serum glutamic oxaloacetic transaminase, AAT

Synonyms: Aspartate Transaminase, Glutamate Oxaloacetate, AST, GOT, sGOT, AspAT, ASAT, serum glutamic oxaloacetic transaminase, AAT, Aspartate Aminotransferase (AST, GOT), Human Liver

Background Information: AST/SGOT is found in many tissues throughout the body, including the liver, heart, muscles, kidney, and brain. If any of these organs or tissues is affected by disease or injury, AST is released into the bloodstream. This means that AST isn't as specific an indicator of liver damage as ALT (also known as alanine aminotransferase, another type of enzyme found almost entirely in the liver). The ratio of AST and ALT levels are commonly used as biomarkers for liver health.

Reconstitution Instructions: ≥ 1 mg/mL in Tris buffered saline, 1% BSA, pH 8.0

NCBI Gene Symbol: GOT1

Gene ID: 2805

NCBI Accession: P17174

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Additional Information

Size:
1 units
Country of Manufacturing Origin:
USA
Country of Animal Origin:
USA
Gene Source:
Human
Recombinant:
No
Source:
Human Liver
Purity by SDS-PAGE:
N/A
Assay:
N/A
Purity:
N/A
Assay 2:
N/A
Endotoxin Level:
N/A
Biological activity:
≥ 1 U/mg (Dimension® Clinical Chemistry System)
Molecular Weight:
~92 kDa
Storage Temperature:
-20°C
Shelf Life:
12 months
Appearance:
lyophilized
Handling:
Centrifuge the vial prior to opening.
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