نتایج جستجو برای: clone library

تعداد نتایج: 156567  

Journal: :Infection and immunity 1986
L B Trevino W G Haldenwang J B Baseman

A genomic library of Mycoplasma pneumoniae was generated by using bacteriophage lambda EMBL3 as the vector. Screening of the library for the expression of M. pneumoniae protein antigens with adsorbed anti-M. pneumoniae serum revealed strong reactivity from a third of those clones which contained mycoplasma DNA inserts. Three of the most highly reactive clones were analyzed in detail and found t...

Journal: :Applied and environmental microbiology 2003
K J Purdy D B Nedwell T M Embley

The distribution and activity of communities of sulfate-reducing bacteria (SRB) and methanogenic archaea in two contrasting Antarctic sediments were investigated. Methanogenesis dominated in freshwater Lake Heywood, while sulfate reduction dominated in marine Shallow Bay. Slurry experiments indicated that 90% of the methanogenesis in Lake Heywood was acetoclastic. This finding was supported by ...

Journal: :Journal of animal science 1993
C B Schmitz M F Rothschild C K Tuggle

Source and Description of Clone. A 1.9-kb partial cDNA insert of porcine a-actinin2 in a pBluescript SKphagemid vector was isolated from a swine adult skeletal muscle cDNA lambda ZAP11 library (kindly provided by Charles Louis, University of Minnesota).

Journal: :Nucleic acids research 1988
C Heinzmann J Ladias S Antonarakis A Diep M Schotz A J Lusis

SOURCE AND DESCRIPTION OF CLONE: A 1.65 kb ECORI cDNA insert corresponding to the full length hepatic lipase (HL) sequence isolated from a rat liver cDNA library (I). CHROMOSOMAL LOCALIZATION: Chromosome 15q21 by somatic cell and in situ hybridization (2).

2015
Kathy N. Lam Trevor C. Charles

BACKGROUND Clone libraries provide researchers with a powerful resource to study nucleic acid from diverse sources. Metagenomic clone libraries in particular have aided in studies of microbial biodiversity and function, and allowed the mining of novel enzymes. Libraries are often constructed by cloning large inserts into cosmid or fosmid vectors. Recently, there have been reports of GC bias in ...

Journal: :Nucleic acids research 1992
M E Zolan J R Crittenden N K Heyler L C Seitz

We have constructed cosmid libraries from electrophoretically separated chromosomes of the basidiomycete Coprinus cinereus. These libraries greatly facilitate the isolation of genes by complementation of mutant phenotypes and are particularly useful for map-based cloning strategies. From a library constructed from two co-migrating C.cinereus chromosomes, we isolated a clone that complements the...

Journal: :The Biochemical journal 1990
K Takazawa J Vandekerckhove J E Dumont C Erneux

Inositol 1,4,5-trisphosphate (InsP3) 3-kinase catalyses the phosphorylation of InsP3 to inositol 1,3,4,5-tetrakisphosphate (InsP4). InsP3 3-kinase activity was stimulated by Ca2+ in the presence of calmodulin (CaM) and the protein was associated with two silver-stained bands which migrated with an apparent Mr of approx. 50,000 on SDS/polyacrylamide gels. Upon limited proteolysis with trypsin, t...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1985
P L Faust S Kornfeld J M Chirgwin

An 1110-base-pair cDNA clone for human cathepsin D was obtained by screening a lambda gt10 human hepatoma G2 cDNA library with a human renin exon 3 genomic fragment. Poly(A)+ RNA blot analysis with this cathepsin D clone demonstrated a message length of about 2.2 kilobases. The partial clone was used to screen a size-selected human kidney cDNA library, from which two cathepsin D recombinant pla...

Journal: :Acta biochimica Polonica 2003
Amr M Shabaan Magdy M Mohamed Mohga S Abdallah Hayat M Ibrahim Amr M Karim

Two Schistosoma mansoni cDNA clones 30S and 1H were identified by immunoscreening of sporocyst lambdagt11 library and by random sequencing of clones from lambdaZap libraries, respectively. Clone 30S was one of 30 clones identified by an antibody raised against tegument of 3-h schistosomules. The clone was found to encode an 81 amino-acid protein fragment. It was expressed in Escherichia coli as...

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