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Cloning and expression of Na^+/I^--symporter

Research Project

Project/Area Number 04671493
Research Category

Grant-in-Aid for General Scientific Research (C)

Allocation TypeSingle-year Grants
Research Field 内分泌・代謝学
Research InstitutionMiyazaki Medical College

Principal Investigator

KOTANI Tomio  Miyazaki Medical College, Laboratory Medicine, Assistant Professor, 医学部, 助教授 (10161936)

Project Period (FY) 1992 – 1993
Project Status Completed (Fiscal Year 1993)
Budget Amount *help
¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 1993: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 1992: ¥1,300,000 (Direct Cost: ¥1,300,000)
KeywordsNa^+ / I^--symporter / cloning
Research Abstract

In order to get a cDNA for Na^+/I^--symporter, I constructed a cDNA library using a expression vector, pCDM8, and mRNA with more than 1 kb molecular size from FRTL-5. The library was divided into 120 pools consisting of 500 to 2,000 E.coli colonies. The plasmid purified from each pool was transfected Cos7 by the dextran method to measure ^<125>I-uptake. However, I could not get any cDNAs for Na^+/I^--symporter in this screening system.
Cosequently, I concluded that Na^+/I^--symporter would not express successfully in Cos7.
As a next attempt, I have made a plan that cDNA for Na^+/I^--symporter should be screened by the procedure of Vilijn, i.e.mRNA transcribed from each plasmid pool in vitro should be injected into Xenopus oocytes to measure their ^<125>I uptake. Since I have no tools for microinjection and have had no experience in microinjection. I have been purchasing microinjection tools and practicing microinjection. Therefore, I have no data about Na^+/I^--symporter cDNA.

Report

(3 results)
  • 1993 Annual Research Report   Final Research Report Summary
  • 1992 Annual Research Report

URL: 

Published: 1992-04-01   Modified: 2016-04-21  

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