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

Reactivity: Human, Mouse
Details: Rabbit IgG Polyclonal
Applications: IHC, WB, ICC/IF
Immunocytochemistry/ Immunofluorescence: CHD7 Antibody - BSA Free [NBP1-77393]
(2)
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Reactivity: Human, Mouse
Details: Rabbit IgG Polyclonal
Applications: IHC, WB, ELISA, ICC/IF
Western Blot: CHD7 AntibodyBSA Free [NBP2-41133]
(3)
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Reactivity: Human
Details: Rabbit IgG Polyclonal
Applications: ICC/IF, ChIP
Immunocytochemistry/ Immunofluorescence: CHD7 Antibody [NBP2-55672]
(2)
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Reactivity: Human
Source: E. coli
Applications: AC
CHD7 Recombinant Protein Antigen
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Reactivity: Human
Source: Sf 9 (baculovirus)
CHD7 Recombinant Enzymes
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Reactivity: Human, Mouse
Details: Rabbit IgG Polyclonal
Applications: IHC, WB, ICC/IF
Novus Antibodies
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Reactivity: Human, Mouse
Details: Rabbit IgG Polyclonal
Applications: IHC, WB, ICC/IF
CHD7 Antibody [CoraFluor™ 1]
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