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151 results for "CHD7" in Products

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 abnormalities, hearing loss, cardiovascular malformations, urogenital anomalies, and growth retardation.

Reactivity: Human
Details: Mouse IgG1 Monoclonal Clone #772503
Reactivity: Human
Details: Sheep IgG Polyclonal
Reactivity: Human
Details: Sheep IgG Polyclonal
Reactivity: Human
Details: Mouse IgG1 Monoclonal Clone #772503
Reactivity: Human
Details: Mouse IgG1 Monoclonal Clone #772503
Reactivity: Human
Details: Sheep IgG Polyclonal
Reactivity: Human
Details: Sheep IgG Polyclonal
Reactivity: Human
Details: Sheep IgG Polyclonal
Reactivity: Human
Details: Sheep IgG Polyclonal
Reactivity: Human
Details: Mouse IgG1 Monoclonal Clone #772503
Reactivity: Human, Mouse
Details: Rabbit IgG Polyclonal
Applications: IHC, WB, ICC/IF
Immunocytochemistry/ Immunofluorescence: CHD7 Antibody - BSA Free [NBP1-77393]
(2)
Reactivity: Human, Mouse
Details: Rabbit IgG Polyclonal
Applications: IHC, WB, ELISA, ICC/IF
Reactivity: Human, Mouse
Details: Rabbit IgG Polyclonal
Applications: IHC, WB, ICC/IF
CHD7 Antibody [CoraFluor™ 1]
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