Abstract
Acetic acid (pH 2.0) treatment denatures chromosomal DNA in situ. Following in situ hybridization cellular and chromosomal morphology is well preserved. For AT-rich DNA sequences the final efficiency of the subsequent hybridization reaction is comparable to the routinely employed NAOH denaturation method, and although there is some discrimination against denaturation of high GC-rich DNA sequences it is less marked than with HCl.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
