A procedure for the preparation of [32P]phosphatidic acid
β Scribed by R.Kennedy Keller; W.Lee Adair; Nancy Cafmeyer
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- English
- Weight
- 546 KB
- Volume
- 155
- Category
- Article
- ISSN
- 0003-2697
No coin nor oath required. For personal study only.
β¦ Synopsis
The phosphorylation procedure of F. Cramer, W. Rittersdorf, and W. Bohm [(1961) Chem. Ber. 654, 180] using bis(triethylammonium) phosphate and trichloroacetonitrile was shown to be effective in the synthesis of [32P]phosphatidic acid. From diacylglyceride and 0.5 mCi H(3)32PO4, 25-50 microCi of labeled material (sp act = 1 mCi/mumol) can be prepared in 2 h. The product was shown to be radiochemically pure by both TLC and HPLC. L- and DL-[32P]dipalmitoyl phosphatidic acid prepared using this procedure were shown to be hydrolyzed by rat liver microsomes at approximately the same rates.
π SIMILAR VOLUMES
Homovanillic acid (4-hydroxy-3-methoxyphenylacetic acid ) was labeled with tritium by exchange reaction in tritiated water catalyzed by sulfuric acid. The product was obtained in gocd yield and specific activities sufficient be utilized in metabolic experiments. Reactions carried out under identical
A simple method for preparing s-32P-labeled nucleoside-5'-triphosphates of high specific activity is presented. Unprotected nucleosides are heated dry with urea and inorganic phosphate. The products from such reactions are phosphorylated enzymatically.