AKR7A3 (Human) Recombinant Protein (P01)
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More Files
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Specification
Product Description
Human AKR7A3 full-length ORF ( AAH25709, 1 a.a. - 331 a.a.) recombinant protein with GST-tag at N-terminal.
Sequence
MSRQLSRARPATVLGAMEMGRRMDAPTSAAVTRAFLERGHTEIDTAFVYSEGQSETILGGLGLRLGGSDCRVKIDTKAIPLFGNSLKPDSLRFQLETSLKRLQCPRVDLFYLHMPDHSTPVEETLRACHQLHQEGKFVELGLSNYAAWEVAEICTLCKSNGWILPTVYQGMYNAITRQVETELFPCLRHFGLRFYAFNPLAGGLLTGKYKYEDKDGKQPVGRFFGNTWAEMYRNRYWKEHHFEGIALVEKALQAAYGASAPSMTSATLRWMYHHSQLQGAHGDAVILGMSSLEQLEQNLAAAEEGPLEPAVVDAFNQAWHLVAHECPNYFR
Host
Wheat Germ (in vitro)
Theoretical MW (kDa)
61.93
Preparation Method
Purification
Glutathione Sepharose 4 Fast Flow
Quality Control Testing
12.5% SDS-PAGE Stained with Coomassie Blue.
Storage Buffer
50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
Storage Instruction
Store at -80°C. Aliquot to avoid repeated freezing and thawing.
Note
Best use within three months from the date of receipt of this protein.
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Applications
Enzyme-linked Immunoabsorbent Assay
Western Blot (Recombinant protein)
Antibody Production
Protein Array
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Gene Info — AKR7A3
Entrez GeneID
22977GeneBank Accession#
BC025709Protein Accession#
AAH25709Gene Name
AKR7A3
Gene Alias
AFAR2
Gene Description
aldo-keto reductase family 7, member A3 (aflatoxin aldehyde reductase)
Omim ID
608477Gene Ontology
HyperlinkGene Summary
Aldo-keto reductases, such as AKR7A3, are involved in the detoxification of aldehydes and ketones.[supplied by OMIM
Other Designations
OTTHUMP00000002623|aflatoxin B1 aldehyde reductase 2|aldo-keto reductase family 7, member A3
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Interactome
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Disease
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Publication Reference
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In vitro metabolism of a novel JNK inhibitor tanzisertib: interspecies differences in oxido-reduction and characterization of enzymes involved in metabolism.
Atsriku C, Hoffmann M, Moghaddam M, Kumar G, Surapaneni S.
Xenobiotica 2015 Jun; 45(6):465.
Application:Enzyme, Human, Tanzisertib were incubated in human liver microsomes, cytosol and hepatocytes.
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In vitro metabolism of a novel JNK inhibitor tanzisertib: interspecies differences in oxido-reduction and characterization of enzymes involved in metabolism.
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