Preparation and characterization of cell-free protein synthesis systems from oocytes and eggs of Xenopus laevis

Clicks: 382
ID: 269741
1989
Free PDF
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Star

Ranked #6 of 13 articles by views in development (cambridge, england)

Most read Least read

Bar heights use a square-root scale.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Sign in to mint
Abstract
During the maturation of the oocytes of the frog Xenopus laevis, the rate of protein synthesis shows a twofold increase. Studies of the mechanisms involved in this stimulation have been seriously limited by the lack of an active cell-free translation system. We have now prepared such systems from oo …
Reference Key
td1989developmentpreparation Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Patrick TD;Lewer CE;Pain VM;;
Journal development (cambridge, england)
Year 1989
DOI
DOI not found
URL
http://www.ncbi.nlm.nih.gov/pubmed/2627883
Keywords
National Center for Biotechnology Information NCBI NLM MEDLINE RNA animals pubmed abstract nih national institutes of health national library of medicine female messenger / metabolism kinetics protein biosynthesis* centrifugation cell-free system oocytes / drug effects progesterone / pharmacology pmid:2627883 t d patrick c e lewer v m pain oocytes / growth & development oocytes / metabolism* ovum / metabolism* transfer amino acyl / metabolism met* xenopus laevis

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

Comments

No comments yet. Be the first to comment on this article.