A powerful method for the preparation of cDNA libraries: isolation of cDNA encoding a 100-kDal nucleolar protein
- 1 January 1985
- Vol. 37 (1-3) , 215-220
- https://doi.org/10.1016/0378-1119(85)90275-6
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- A simplified and efficient vector-primer cDNA cloning systemGene, 1984
- Three different fibronectin mRNAs arise by alternative splicing within the coding regionCell, 1983
- Yeast RNA Polymerase II Genes: Isolation with Antibody ProbesScience, 1983
- A simple and very efficient method for generating cDNA librariesGene, 1983
- Detection and Localization of a Class of Proteins Immunologically Related to a 100‐kDa Nucleolar ProteinEuropean Journal of Biochemistry, 1982
- General method for cloning amplified DNA by differential screening with genomic probes.Molecular and Cellular Biology, 1982
- High-efficiency cloning of full-length cDNA.Molecular and Cellular Biology, 1982
- 5′-Terminal sequences of eucaryotic mRNA can be cloned with high efficiencyNucleic Acids Research, 1981
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970
- A physical study by electron microscopy of the terminally repetitious, circularly permuted DNA from the coliphage particles of Escherichia coli 15Journal of Molecular Biology, 1970