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  1. ...-specific oligonucleotide primer. Proc. Natl. Acad. Sci. 85 : 8998 – 9002 . 5. Lorens, J.B., unpublished. Sambrook, J., E.F. Fritsch, and T. Maniatis. 1989. Molecular cloning: A laboratory manual . Cold Spring Harbor Laboratory, New York. 7. Wilson, V.G. Wilson, V.G. 1988 . A rapid procedure for removal of excess linkers...
  2. ...co-directional LoxP sites, enabling 143 cleavage by Cre recombinase (Figure 2B). We tested five different introns to accommodate the 144 upstream LoxP site, including an artificial intron (Guzzardo et al. 2017), chimeric intron from CAG 145 8 promotor, a mutated form of the chimeric intron (mut...
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  3. ...the control of cell-type-specific promotors; therefore, its expression is confined into a group of cells instead of a single cell (Chen et al. 2022). This strategy often leads to sparsely distributed clones across a sample, making it challenging to distinguish clones from one another (Kester and van...
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  4. ...(Supplemental Fig. S4G). Successful transmissions of the two loxP sites were also confirmed by PCR (Supplemental Fig. S4H) and sequencing (Fig. 2E, boxed panels).A cloning-based strategy to rapidly identify founders with loxP insertions in cisBy Mendel's law of inheritance, the simultaneous transmission of 5...
  5. ...vectors, is based on the Cre- loxP -based site-specific recombination system of bacteriophage P1 ( Sternberg et al. 1981 ). Both Clontech systems are well-suited to automated methods. Creating Master Clones With In-Fusion Like the Gateway system, Clontech master (Donor) clones can be assembled using...
  6. ...containing recombination sites and incubated with bacteriophage λ integrase recombination proteins to accomplish the transfer of the gene into the new vector. We refer to this process as recombinational cloning (RC). Our experiments initially used both the bacteriophage λ system and the Cre/ lox P system...
  7. ...is used for the initial cloning of PCR products, whereas the pHOST plasmid contains the appropriate promoter or tag sequences for creating fusion proteins. The recombinant protein expression construct is made by fusion of the pUNI and pHOST plasmids via Cre- loxP site–specific recombination ( Fig. 1 ; Liu...
  8. ...extensive scrambling has impacted Hox cluster organization in bryozoans. We annotated the Hox genes of the five bryozoan species (Supplemental Fig. S12; Supplemental Data S2) and identified extensive gene loss in the bryozoan Hox gene set, which lacks Hox1, Hox3, Scr, Antp, Lox2, and Post1 in all five...
  9. ...Concerted Assembly and Cloning of Multiple DNA Segments Using In Vitro Site-Specific Recombination: Functional Analysis of Multi-Segment Expression Clones David L. Cheo 1 , 2 , Steven A. Titus 1 , 2 , Devon R.N. Byrd 2 , 3 , James L. Hartley 2 , 4...
  10. ...the achievable mapping resolution of QTL, posing a serious threat to the efficacy of positional (candidate) cloning for QTL considerably. QTL mapping efforts, whether performed in pedigrees or by exploiting linkage disequilibrium, are likely to leave geneticists with a portion of the that contains tens...
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