Abstract
In wheat leaf and root crude extracts several RNases can be distinguished by pH optima analysis, and SDS-PAGE and activity staining. One acidic RNase (approximately 20 kD in size) and a group of neutral RNases have been identified by electrophoretic separation. Neutral RNases can be divided into salt-stimu- lated (about 24 and 26 kD) and salt-inhibited (about 27kD). Following low temperature treatment, acidic and neutral salt-inhibited RNases remain unchanged, while the neutral salt-stimulated RNases with higher mobility generally increase with respect to the control.
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.
