Zobrazeno 1 - 9
of 9
pro vyhledávání: '"G. S. Ghangas"'
Publikováno v:
Journal of bacteriology. 173(11)
The DNA sequences of the Thermomonospora fusca genes encoding cellulases E2 and E5 and the N-terminal end of E4 were determined. Each sequence contains an identical 14-bp inverted repeat upstream of the initiation codon. There were no significant hom
Autor:
G S Ghangas, R Wu
Publikováno v:
Journal of Biological Chemistry. 250:4601-4606
Procedures have been worked out for Aspergillus nuclease S1 and mung been nuclease to quantitatively cleave off both of the 12-nucleotide long, single-stranded cohesive ends of lambdaDNA. This cleavage is indicated by the almost complete elimination
Autor:
D B Wilson, G S Ghangas
Publikováno v:
Journal of Bacteriology. 157:158-164
Salmonella DNA was partially digested with EcoRI, and the digest was fractionated to obtain fragments larger than 8 kilobases (kb). These were ligated into EcoRI-cut pBR322, and the mixture was used to transform Salmonella Xyl- cells selecting for am
Autor:
G S, Ghangas, R, Wu
Publikováno v:
The Journal of biological chemistry. 250(12)
Procedures have been worked out for Aspergillus nuclease S1 and mung been nuclease to quantitatively cleave off both of the 12-nucleotide long, single-stranded cohesive ends of lambdaDNA. This cleavage is indicated by the almost complete elimination
Thermomonospora fusca chromosomal DNA was partially digested with EcoRI to obtain 4- to 14-kilobase fragments, which were used to construct a library of recombinant phage by ligation with EcoRI arms of lambda gtWES. lambda B. A recombinant phage codi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::694fc17f34e06154649e94c5ddcd5f1e
https://europepmc.org/articles/PMC210001/
https://europepmc.org/articles/PMC210001/
Autor:
G S, Ghangas, R, Wu
Publikováno v:
The Journal of biological chemistry. 249(23)
Publikováno v:
Chemischer Informationsdienst. 5
Publikováno v:
Somatic cell genetics. 5(6)
Three 6-thioguanine-resistant mutants of the human diploid lymphoblast line MGL-8 were studied. The inactivation by heat of both HGPRT activity and antigenicity of the HGPRT immunologically cross-reacting material of the A30 mutant cells were not pro
Publikováno v:
Biochemical and biophysical research communications. 54(3)