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The fractionation of high-molecular-weight ribonucleic acid by polyacrylamide-gel electrophoresis

1. Gels were prepared with recrystallized acrylamide and bisacrylamide. Electrophoresis was in tris–sodium acetate–EDTA buffer for 0·5 to 3hr. Gels were scanned at 280 or 265mμ. Techniques are described for slicing and radioactive counting. 2. The mobility of RNA was inversely related to the sedimen...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile nagusia: Loening, U. E.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1967
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1270235/
https://ncbi.nlm.nih.gov/pubmed/5339944
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