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
>Phosphate Assay
>Preparation of 
>Neutralizing Arachi
>Purification of&nbs
>Methylation of 
>Lipid analysis:Thi
>Liposome Swelling&n
>Lipid analysis-Wee
>Liposome Preparatio
>Sphingomyelin Mass&
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 by Suprya Jaydev
[ 文章来源: | 文章作者: | 发布时间:2007-07-06|  字体: [ ]  

Phosphate Assay by Suprya Jaydev



Contributor: Suprya Jayadev
Date: Sep. 8, 1994



Reagents

Ashing buffer:

10 g Mg(NO3)2
100 ml EtOH

1.5 N HCl stock:

119.7 ml concentrated HCl (11.6M @ 36% by weight)
880.3 ml H2O

1 N Sulfuric acid stock:

28.9 ml concentrated sulfuric acid (18M/36N @ 96% by weight)
971.1 ml H2O

Ammonium molybdate stock:

4.2 ml Ammonium molybdate
1000 ml 1N H2SO4



Procedure

1) Prepare standards in duplicate.

--> standards: 0, 3, 5, 7, 10, 12, and 15 µl of a 1 mM NaH2PO4 stock solution

2) Aliquot lipid unknowns.

3) Add 100 µl ashing buffer to each sample.

4) Dry EtOH and chloroform from samples by heating @ 80°C for ~20 minutes.

5) Flame samples using a strong flame on the bunsen burner.

6) Remove samples from flame when the brown gas ceases to be released.

--> There should be a white percipitate remaining at the base of the tubes. If the ashing process is allowed to proceed for too long, the percipitate will appear brown/charred and this will skew the spectrophotometer readings.

7) Add 0.3 ml of 0.5N HCl to each sample and boil for 15 minutes.

8) To each tube, add:

0.6ml ammonium molybdate
0.1 ml ascorbic acid (10% w/v, made fresh EACH time)

VORTEX!!

9) Incubate for 30 minutes @ 45°C or for 60 minutes @ 37°C.

10) Read OD820.


上一篇:Phosphate Assay   下一篇:Preparation of bOG-DOPG mixed micelles
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