購物車
幫助
021-54845833/15800441009
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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. |
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Applications: |
ELISA, WB, IHC |
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Name of antibody: |
TAT |
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Immunogen: |
Fusion protein of human TAT |
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Full name: |
tyrosine aminotransferase |
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SwissProt: |
P17735 |
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ELISA Recommended dilution: |
1000-2000 |
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IHC positive control: |
Human colon cancer and Human liver cancer |
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IHC Recommend dilution: |
25-100 |
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WB Predicted band size: |
50 kDa |
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WB Positive control: |
Human normal liver tissue |
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WB Recommended dilution: |
200-1000 |
