The assay begins with a standard kinase reaction performed in the provided reaction Buffer with a provided Bisamide Rhodamine 110 peptide substrate (PKA R110 substrate).
检测开始时、先用试剂盒提供的PKA双酰胺罗丹明110肽底物进行一个标准的激酶反应。
The acidity for hydride generation reaction, selection of buffer solution and oxidizer, dynamic linear range, interference from coexistent elements and their elimination were studied.
主要对锗、锡的氢化反应酸度，缓冲溶液的选择，动态线性范围，氧化剂的选择，共存元素的干扰及其消除进行了实验。
The acidity for hydride generation reaction, selection of buffer solution and oxidizer, dynamic linear range, interference from coexistent elements and their elimination were studied.
主要对锗、锡的氢化反应酸度，缓冲溶液的选择，动态线性范围，氧化剂的选择，共存元素的干扰及其消除进行了实验。
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