首 页网站地图RSS订阅高级搜索保留
生物实验网
设为首页
加入收藏
站长信箱
主页|bio资讯 |DNA实验 |PCR实验 |RNA实验 |蛋白实验 |基本实验技术 |生化与免疫技术 |生物信息学 |细胞生物学 |杂交实验 |学科相关 |交叉领域 |
当前位置: 主页>生化与免疫技术>脂肪与糖类实验> 查看文章详细内容
站内资料搜索
热门关键字: dna  EST  r DNA  pcr  抗体  rt pcr  t dna  tail pcr  PCR sscp  cDNA

相关文章
>Neutralizing Arachi
>Phosphate Assay&nbs
>Methylation of 
>Preparation of 
>Liposome Swelling&n
>Purification of&nbs
>Liposome Preparatio
>Lipid analysis:Thi
>Labeled Sphingomyel
>Lipid analysis-Wee
热点文章
Dynamic Flow A
Analysis of Ol
Detection of G
Measurement of 
DGK Assay
Carbohydrate-Specific&nb
Immunostaining Thin
AA & Metabolit
Carbohydrate Assays
Lipid analysis:EXT
Phosphate Assay
[ 文章来源: | 文章作者: | 发布时间:2007-07-06|  字体: [ ]  

Phosphate Assay

Contributor: Jiandi Zhang
Date: July 4, 1996


1. Make standards using sodium phosphate at the following uM concentrations: 0, 2, 5, 7, 10, 20, 40, 60, and 80. Use the screw top glass tubes.

2. Dry the samples and standards under nitrogen evaporator (Rm 209), and add 150 ul 70% perchloric acid. Oxidize the samples and standards in a heating block (180C, Rm 218) overnight or for 1 hour if the heating block has been pre-heateed.

3. Rinse the sides of the tubes with 830ul xenopure water and vortex.

4. Add 170 ul 2.5% ammonium molybdate (by weight) and vortex.

5. Add 170 ul 10% ascorbic acid (by weight) and vortex. Make the ascorbic acid fresh every time.

6. Incubate for 15 min at 50°C. Allow tubes to cool.

7. Use spectrophotometer to read absorbance at 820nm.


上一篇:Neutralizing Arachidonic Acid   下一篇:Phosphate Assay by Suprya Jaydev
设为首页 - 加入收藏 - 关于我们 - 版权申明 - 程序支持 - 联系方式 - 留言薄 - 会员中心
Power by DedeCms