4 results for "CHD7" in 产品
CHD7 Products
Human CHD7 is a chromodomain helicase DNA-binding protein and mutations in the CHD7 gene are a major cause of CHARGE syndrome. CHARGE syndrome is a well characterized multiple-malformation syndrome with distinctive diagnostic critera. Anomalies include ocular coloboma, choanal atresia, cranial nerve defects, distinctive external and inner ear abnor...
| Reactivity: | Human, Mouse |
| Details: | Rabbit IgG Polyclonal |
| Applications: | IHC, WB, ICC/IF |
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| Reactivity: | Human |
| Details: | Sheep IgG Polyclonal |
| Applications: | WB, ICC/IF |
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| Reactivity: | Human |
| Details: | Mouse IgG1 Monoclonal Clone #772503 |
| Applications: | ICC/IF |
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| Reactivity: | Human, Mouse |
| Details: | Rabbit IgG Polyclonal |
| Applications: | IHC, WB, ELISA, ICC/IF |
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