Tissue expression
Cell line expression
Protein structure
TAT
Tyrosine aminotransferaseThis nuclear gene encodes a mitochondrial protein tyrosine aminotransferase which is present in the liver and catalyzes the conversion of L-tyrosine into p-hydroxyphenylpyruvate. Mutations in this gene cause tyrosinemia (type II, Richner-Hanhart syndrome), a disorder accompanied by major skin and corneal lesions, with possible cognitive disability. A regulator gene for tyrosine aminotransferase is X-linked. [provided by RefSeq, Jul 2008]
Top validated antibodies |
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antibodies-online | ABIN955086 | 5 references | Polyclonal |
WB
IHC
FC
|
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Aviva Systems Biology | OAAB06130 | Polyclonal |
WB
EL
IHC
FC |
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Novus Biologicals | 46420002 | 2 references | Polyclonal |
WB
EL |
|
Acris Antibodies GmbH | AP54159PU-N | Polyclonal |
WB
IHC
FC
|
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OriGene | AP54159PU-N | Polyclonal |
WB
IHC
FC
|
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Supportive data in Antibodypedia
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