Abstract
A kinetic, two-point method for the assay of α-arnylase in serum, involving spectrohotometric measurement of a starch-iodine complex, is described. This approach avoids interferences by serum proteins and other substances that react with iodine. The method requires less than 4 min per assay, only 10 μl of sample is used, and precision and accuracy are comparable to those of established procedures.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: 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.