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You are here:Home » Antibodies » Abs to Disease Markers » Anti -CHD7 (Chromodomain-helicase-DNA-binding Protein 7, CHD-7, ATP-dependent Helicase CHD7, KIAA1416)

Anti -CHD7 (Chromodomain-helicase-DNA-binding Protein 7, CHD-7, ATP-dependent Helicase
CHD7, KIAA1416)

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Specifications

Clone Host Grade Applications
Polyclonal Goat Affinity Purified E
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.
Catalog #C3880-51B
ApplicationsSuitable for use in ELISA. Other applications not tested.
Recommended DilutionELISA: 1:64,000
Optimal dilutions to be determined by the researcher.
Storage and StabilityMay be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are stable for at least 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Clone TypePolyclonal
IsotypeIgG
HostGoat
SourceHuman
Concentration~0.5mg/ml
FormSupplied as a liquid in Tris saline, 0.02% sodium azide, pH7.3, 0.5% BSA.
PurityPurified by immunoaffinity chromatography.
ImmunogenSynthetic peptide corresponding to C-KDEIDEFANSPSE, from the internal region of the protein sequence according to NP_060250.2.
SpecificityRecognizes CHD7. Species sequence homology: human, mouse and rat.
Important NoteThis product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.


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