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TAT Polyclonal Antibody, 50ul Hybridoma Antibody Sequencing Mutations in this gene are
TAT Polyclonal Antibody, 50ul Hybridoma Antibody Sequencing Mutations in this gene are
TAT Polyclonal Antibody, 50ul Hybridoma Antibody Sequencing Mutations in this gene are
TAT Polyclonal Antibody, 50ul Hybridoma Antibody Sequencing Mutations in this gene are

TAT Polyclonal Antibody, 50ul Hybridoma Antibody Sequencing Mutations in this gene are

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TAT Polyclonal Antibody, 50ul Hybridoma Antibody Sequencing Mutations in this gene areThis nuclear gene TAT (tyrosine aminotransferase) encodes a mitochondrial protein tyrosine aminotransferase which is present in the liver and catalyzes the conversion of L tyrosine into p hydroxyphenylpyruvate. Mutations in TAT cause tyrosinemia (type II, Richner Hanhart syndrome), a disorder accompanied by major skin and corneal lesions, with possible mental retardation. A regulator gene for tyrosine aminotransferase is X linked.

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Description

Mutations in this gene are associated with Ehlers-Danlos syndrome types IV

The second intron contains an apparently intronless gene

The protein encoded by this gene belongs to the SMAD

while the paper/plastic packaging keeps them sterile

TAT Polyclonal Antibody, 50ul Hybridoma Antibody Sequencing Mutations in this gene areThis nuclear gene TAT (tyrosine aminotransferase) encodes a mitochondrial protein tyrosine aminotransferase which is present in the liver and catalyzes the conversion of L tyrosine into p hydroxyphenylpyruvate. Mutations in TAT cause tyrosinemia (type II, Richner Hanhart syndrome), a disorder accompanied by major skin and corneal lesions, with possible mental retardation. A regulator gene for tyrosine aminotransferase is X linked.

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