TAT (BC020707) Human Untagged Clone
TAT (untagged)-Homo sapiens, Similar to tyrosine aminotransferase, clone MGC:22474 IMAGE:4710626, complete cds
|Product Name||TAT (BC020707) Human Untagged Clone|
|Type||Human Untagged Clone|
|Synonyms||tyrosine aminotransferase; tyrosine aminotransferase, cytosolic|
|E. coli Selection||Ampicillin (100 ug/mL)|
>NCBI ORF sequence for BC020707, the custom clone sequence may differ by one or more nucleotides
>OriGene 5' read for BC020707 unedited
|Insert Size||4000 bp|
|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.|
|Reconstitution||1. Centrifuge at 5,000xg for 5min.
2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA.
3. Close the tube and incubate for 10 minutes at room temperature.
4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom.
5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C.
|RefSeq Size||1116 bp|
|RefSeq ORF||1116 bp|
|Protein Families||Druggable Genome, Embryonic stem cells, ES Cell Differentiation/IPS|
|Protein Pathways||Cysteine and methionine metabolism, Metabolic pathways, Phenylalanine, tyrosine and tryptophan biosynthesis, Phenylalanine metabolism, Tyrosine metabolism, Ubiquinone and other terpenoid-quinone biosynthesis|
|Gene 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 cognitive disability. A regulator gene for tyrosine aminotransferase is X-linked. [provided by RefSeq, Jul 2008]|
|cDNA Clone Resources|