Yamamoto R, Kimura S, Hattori S, Matsuura A, Hayakawa T
Clin Chem. 1985 Apr;31(4):628-30.
This practical assay for measuring insulin involves use of a 4 X 8 mm chromatographic column. Serum samples are incubated at 30 degrees C for 1 h with beta-D-galactosidase-labeled antibody to insulin, then passed through the 0.1-mL column containing insulin immobilized on Sepharose 4B. After the column is washed to remove the bound label, the buffer in the column is replaced with a solution of o-nitrophenyl-beta-D-galactoside. The column is then incubated at 30 degrees C for 1 h, the enzyme reaction is stopped by washing the column with sodium carbonate solution, and the absorbance of the eluate is measured at 420 nm. Results obtained by this method were compared with those by a radioimmunoassay and a solid-phase enzyme immunoassay.
这种用于测量胰岛素的实用检测方法涉及使用一根4×8毫米的色谱柱。血清样本与β-D-半乳糖苷酶标记的抗胰岛素抗体在30℃下孵育1小时,然后通过含有固定在琼脂糖4B上的胰岛素的0.1毫升色谱柱。在色谱柱被洗涤以去除结合的标记物后,色谱柱中的缓冲液被邻硝基苯基-β-D-半乳糖苷溶液取代。然后将色谱柱在30℃下孵育1小时,通过用碳酸钠溶液洗涤色谱柱来终止酶反应,并在420纳米处测量洗脱液的吸光度。将通过这种方法获得的结果与放射免疫测定法和固相酶免疫测定法的结果进行比较。