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C3880-51C Goat Anti-CHD7 (Chromodomain-helicase-DNA-binding Protein 7, CHD-7, ATP-dependent Helicase CHD7, KIAA1416)

Specifications
References
Clone Type
Polyclonal
Host
Goat
Source
Human
Isotype
IgG
Grade
Affinity Purified
Applications
E
Crossreactivity
Hu Mo Rt
Accession #
NP_060250.2
Gene ID
55636, 320790, 312974
Shipping Temp
Blue Ice
Storage Temp
-20°C

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.

Applications
Suitable for use in ELISA. Other applications not tested.
Recommended Dilution
ELISA: 1:64,000 Optimal dilutions to be determined by the researcher.
Storage and Stability
May 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.
Immunogen
Synthetic peptide corresponding to C-KDEIDEFANSPSE, from CHD7, at the internal region of the protein sequence (NP_060250.2).
Form
Supplied as a liquid in Tris saline, 0.02% sodium azide, pH 7.3, 0.5% BSA.
Purity
Purified by immunoaffinity chromatography.
Specificity
Recognizes CHD7. Species sequence homology: Human, mouse and rat.
References
1. Gao X, Gordon D, Zhang D, Browne R, Helms C, Gillum J, Weber S, Devroy S, Swaney S, Dobbs M, Morcuende J, Sheffield V, Lovett M, Bowcock A, Herring J, Wise C. CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis. Am J Hum Genet. 2007 May;80(5):957-65. Epub 2007 Mar 12.
USBio References
No references available
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