Garg U C, Rai N, Singh Y, Dhaunsi G S, Sidhu G S, Ganguly N K, Bhatnagar R
Post Graduate Institute of Medical Education and Research, Chandigarh, India.
Biotechniques. 1988 Apr;6(4):294-6.
The activity of calmodulin as an activator of cAMP phosphodiesterase was assayed. AMP was hydrolyzed by 5'-nucleotidase, and the adenosine formed was measured by both liquid scintillation counting and spectrophotometry at 265 nm. Calmodulin activities measured by the two methods were equivalent, indicating that spectrophotometric assay of calmodulin can be used in place of the isotopic method.
对作为环磷酸腺苷磷酸二酯酶激活剂的钙调蛋白活性进行了测定。5'-核苷酸酶可水解AMP,通过液体闪烁计数法和在265nm处的分光光度法来测定生成的腺苷。用这两种方法测得的钙调蛋白活性相当,这表明钙调蛋白的分光光度法测定可替代同位素法。