首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Determination of total proteins in several tissues of rat a comparative study among spectrophotometric mehods
【24h】

Determination of total proteins in several tissues of rat a comparative study among spectrophotometric mehods

机译:分光光度法比较大鼠几种组织中总蛋白的含量

获取原文
获取原文并翻译 | 示例
       

摘要

In the present paper,five spectrophotoetric mehods-biuret,Lowry modified by Hartree (Lowry/Hartree),p-chloranil,ultraviolet at 280 nm (UV-280 nm),and ultraviolet at 260/280 nm)-were used for protein determination in several rat tissues and the results were compared.The lowry/Harttee method showed the highest sensitivity(0.9 #mu#g/ml) and the biuret method the lowest sensitivity(55.7 #mu#g/ml).Theresults were not statistically different for the following mehtods and tissues:Lowry/Hartree was compared to biuret for five tissues (adrenal,spleen,whole brain,liver and small intestine),to p-chloranil for two tissues (liver and epilidymal fat pad),and to UV-260/280 nm for three tissues (whol brain,liver and pancreas).Since the Lowry/Hartree method needs a larger period of time for a whole assay to be carried out,we recommend for determination of total protein the following methods:UV-260/280 nm for whole brain,liver,and pancreas,p-chloranil for epilidymal fat pad,and biuret for other tissues.We do not recommend the UV-280 nm method because there are many interfering substances inthe tissues.
机译:本文采用五种分光光度法-缩二脲,经Hartree修饰的Lowry(Lowry / Hartree),对氯苯胺,在280 nm(UV-280 nm)的紫外线和在260/280 nm的紫外线)的蛋白质测定方法Lowry / Harttee法的敏感性最高(0.9#mu#g / ml),Biuret法的敏感性最低(55.7#mu#g / ml),结果无统计学差异。对于以下方法和方法:将Lowry / Hartree与缩二脲分别用于五种组织(肾上腺,脾脏,全脑,肝脏和小肠),对氯苯胺用于两种组织(肝脏和上皮脂肪垫),并与UV-三种组织(人脑,肝和胰腺)的波长为260/280 nm。由于Lowry / Hartree方法需要较长的时间才能进行整个测定,因此建议使用以下方法测定总蛋白:整个大脑,肝脏和胰腺为260/280 nm,上睑板脂肪垫为对氯苯甲醚,其他组织为缩二脲。我们不建议使用UV-280 nm方法,因为组织中存在许多干扰物质。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号