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Home TrueClone TAT Clone

TAT (NM_000353) Human cDNA Clone

Specifications Citations Clones of Other Species Product Documents
SKU Description Price Availibility*  
SC119924 TAT (untagged)-Human tyrosine aminotransferase (TAT), nuclear gene encoding mitochondrial protein (10ug), NM_000353.1, 10ug $680 In Stock
TF81001 TurboFectin, High performance Transfection reagent (1ml/vial) $420 In Stock
TA311082 Rabbit Monoclonal antibody against Tyrosine Aminotransferase (TAT), 100ul $325 In Stock
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OriGene Data
Vector:pCMV6-XL4 Insert Size: 3860 Restriction Site: NotI-NotI
Sequence Data: Fully Sequenced ORF          5' Read Nucleotide Sequence          3' Read Nucleotide Sequence         
OTI Disclaimer: Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
Product Components: The cDNA clone is shipped in a 2-D bar-coded Matrix tube as dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. Every lot of primer is tested to provide clean sequencing of OriGene TrueClones.
Protein Families: ES Cell Differentiation/IPSEmbryonic stem cellsDruggable Genome
Protein Pathways: Ubiquinone and other terpenoid-quinone biosynthesisCysteine and methionine metabolismTyrosine metabolismPhenylalanine metabolismPhenylalanine, tyrosine and tryptophan biosynthesisMetabolic pathways
Reference Data
RefSeq: NM_000353.1, NP_000344
RefSeq Size: 2754 RefSeq ORF: 1365
Synonyms : tyrosine aminotransferase, cytosolic; tyrosine aminotransferase
LocusID: 6898 Cytogenetic: 16q22.1 Domains: aminotran_1_2
Summary: This 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 mental retardation. A regulator gene for tyrosine aminotransferase is X-linked. [provided by RefSeq, Jul 2008].


* Delivery time is an estimate in business days. Occasional delays may occur due to unforeseen complexities in the preparation of your construct. International customers may expect an additional 1-2 weeks in shipping

 

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