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番茄POD与EST同工酶PAGE方法研究
引用本文:陈启林,巩振辉,陈静. 番茄POD与EST同工酶PAGE方法研究[J]. 西北农业学报, 1999, 8(1): 87-90
作者姓名:陈启林  巩振辉  陈静
作者单位:西北农业大学园艺系, 陕西杨陵 712100;西北农业大学园艺系, 陕西杨陵 712100;西北农业大学园艺系, 陕西杨陵 712100
摘    要:对番茄种子芽期过氧化物酶(POD)同工酶与酯酶(EST)同工酶聚丙烯酰胺凝胶电泳(PAGE)方法进行了初步研究。结果表明,POD同工酶电泳酶样提取液以pH6.5 ̄0.1mol/L磷酸缓冲液+0.1%巯基乙醇较适宜;EST同工酶酶样提取液以pH6.0 ̄7.0的0.1mol/LTris-柠檬酸+0.1%巯基乙醇或0.1mol/L磷酸缓冲液+0.1%巯基乙醇较适宜。常用的7.5%分离胶浓度不适宜番茄种子

关 键 词:番茄 过氧化物酶 酯酶 同工酶 电泳 品种
收稿时间:1997-10-13
修稿时间:1997-12-22

Study on PAGE Method of POD and EST Isozyme in Tomato Seed
Chen Qilin,Gong Zhenhui and Chen Jing. Study on PAGE Method of POD and EST Isozyme in Tomato Seed[J]. Acta Agriculturae Boreali-occidentalis Sinica, 1999, 8(1): 87-90
Authors:Chen Qilin  Gong Zhenhui  Chen Jing
Affiliation:Northwestern Agricultural University, Yangling Shaanxi 712100;Northwestern Agricultural University, Yangling Shaanxi 712100;Northwestern Agricultural University, Yangling Shaanxi 712100
Abstract:Study on PAGE method of POD and EST isozyme in tomato germinating seeds was carried out,the results indicated that the suitable extraction buffer for POD isozyme is pH6.5~7.5 0.1 mol/L, phosphate buffer +0.1% mercaptoethanol,and that for EST isozyme is pH 6.0~7.0 0.1 mol/L. Triscitrate +0.1% mcrcaptoethanol or 0.1 mol/L phosphate buffer +0.1 mol/L. mercaptoethanol. The 7.5% separating gel concentration was not suitable for both isozymes in question,it should be replaced with 11.5% concentration in order to achieve satisfactory electrophoresis effect.
Keywords:Tomato  POD  EST  Isozyme electrophoresis
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