| 产品详情 |
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| Product Name | Homogentisate 1,2-Dioxygenase (HGD) peptide |
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| Description | Homogentisate 1,2-dioxygenase (HGD) gene mutations are the molecular cause of alkaptonuria, a rare hereditary disorder of the phenylalanine catabolism. The highest expression of HGD is in the prostate, small intestine, colon, and liver. |
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| Size | 100 µg |
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| Concentration | n/a |
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| Applications | Western Blotting (WB),Immunohistochemistry (IHC),Blocking Peptide (BP) |
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| Other Names | CG4779|Dmel\\CG4779|PSPTO3551|DDBDRAFT_0185702|DDBDRAFT_0191461|DDB_0185702|DDB_0191461|Hgo|aku|hgo|AKU|HGO |
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| Gene, Accession, CAS # | n/a |
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| Catalog # | ABIN939893 |
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| Price | |
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| Order / More Info | Homogentisate 1,2-Dioxygenase (HGD) peptide from ANTIBODIES-ONLINE GmbH |
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| Product Specific References | n/a |
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| 产品资料 |
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