| No | Size | Price | Availability | |
| YRP01912-01 | 50ul | 1500.00 | In Stock |  |
| YRP01912-01 | 100ul | 2000.00 | In Stock | |
| Source: | Rabbit | Gene Id: | 6898 |
| Isotype: | IgG | Swiss Prot: | |
| purity: | Purified by Protein A. |
| Background: |
| 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. |
| Reactivity | Human, Mouse, Rat |
| Tested applications | WB IHC IF |
| Clonality | Polyclonal Antibody |
| Calculated MW | / |
| Recommended Dilutions |
WB 1:100-1:1000
IHC 1:100-1:500
IF 1:50-1:200
|
| Immunogen | KLH conjugated synthetic peptide derived from human TAT/ATTY |
| Storage | Aqueous buffered solution containing 100ug/ml BSA, 50% glycerol and 0.09% sodium azide. Store at -20℃ for 12 months |
| Synonym | TYROSINE AMINOTRANSFERASE, tyrosine aminotransferase, MGC37772, MGC37789, MGC37790, MGC37819, MGC37828, MGC37842, TAT, ATTY_HUMAN, L-tyrosine:2-oxoglutarate aminotransferase, TAT, Tyrosine aminotransferase, Tyrosine aminotransferase, cytosolic. |
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