| 摘要 |
PCT No. PCT/SE83/00190 Sec. 371 Date Jan. 5, 1984 Sec. 102(e) Date Jan. 5, 1984 PCT Filed May 10, 1983 PCT Pub. No. WO83/04054 PCT Pub. Date Nov. 24, 1983.A method of determining dTk isoenzyme levels of a human or animal body fluid or cell sample is disclosed, which comprises the steps of reacting said sample with a substrate for said isoenzyme in the presence of a phosphate donor and a buffer system, and measuring the amount of phosphorylated product formed, said amount being proportional to said isoenzyme level. The method is characterized by using in combination (a) a buffer system at pH ranging from 5 to 9 and being present in a concentration of no more than 250 mM, (b) a substrate consisting of 2'-deoxy-5-halouridin, part of which has a radio-labelled 5-halogen, and being present in a concentration ranging from 2x10-9-5x10-6M, and (c) the phosphate donor being present in a concentration not exceeding 20 mM. The sensitivity of the method permits measurement of minute amounts of dTk, and the method can be used for e.g. diagnosis, prognostics and monitoring of diseases involving alterated ATP mediated dTk activity, such as cancers, tumors, and certain virus infections, or alterated CTP mediated dTk activity, such as HSV type 1, type 2, and VZV infections.
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