Molecular cloning of a diacylglycerol kinase isozyme predominantly expressed in human retina with a truncated and inactive enzyme expression in most other human cells

In order to clone novel diacylglycerol kinase (DGK) isozymes, we first obtained a DGK-related cDNA fragment by polymerase chain reaction using the human hepatoma cell line HepG2 mRNA and degenerated primers. The amplified fragment was subsequently used as a probe for screening the cDNA library from...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Masayuki Kai, Fumio Sakane, S Imai, Ikuo Wada, Hideo Kanoh
Aineistotyyppi: Artigo
Kieli:englanti
Julkaistu: 1994
Linkit:https://doi.org/10.1016/s0021-9258(17)32336-0
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