| 产品名称： | pRE107 plasmid in E. coli |
|---|---|
| 商品货号： | TS204663 |
| Designations： | pRE107 plasmid in E. coli |
| Depositors： | DM Schifferli, University of Pennsylvania School of Veterinary Medicine, Philadelphia, PA |
| Biosafety Level： | 1 |
| Host： | Escherichia coli SM10 lambda pir |
| Vector Information： | Size (kb): 6.55
Vector: pRE107 (plasmid)
Construction: pGP704, sacB1 (pUC58)
Marker(s): ampR,sacB
Construct size (kb): 6.55
Features: marker(s): ampR marker(s): sacB1 replicon: conditional R6K ori replicon: oriT MCS: PstI...EcoRI restriction site: EcoRI HindIII |
| Applications： | Counterselection levansucrase Suicide vector Vector permitting allelic exchange of cloned inserts |
| Comments： | Restriction digests of the clone give the following sizes (kb): BamHI-- 3.2, 1.7, 1.5; XbaI-- 6.55; EcoRI-- 4.0, 2.8. The sacB1 allele is a variant of sacB with certain restriction sites removed by site directed mutagenesis. Expression of sacB confers sensitivity to sucrose. The conditional R6K origin of replication requires that the pi protein be expressed in trans for plasmid maintenance. One of four allelic exchange suicide vectors (TS204663 - 87694) that provide both selection for chromosomal integration (ampR, cmlR, kanR or tetR) and counterselection for loss of vector DNA and the wild type allele. Construct is suicide plasmid in any host not expressing pir. Cloned inserts may be integrated into the host chromosome (a single recombination event) following electroporation and appropriate antibiotic selection. Negative selection for sucrose sensitivity (sacB) selects for a second recombination event resulting in loss of vector DNA. |
| Media： | ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin |
| Growth Conditions： | Temperature: 37°C |
| References： | Chang TW, et al. Immunoassay for biologically active human interferon-gamma employing unique monoclonal antibodies. US Patent 4,666,865 dated May 19 1987 Edwards RA, et al. Improved allelic exchange vectors and their use to analyze 987P fimbria gene expression. Gene 207: 149-157, 1998. PubMed: 9511756 Donnenberg MS, Kaper JB. Construction of an eae deletion mutant of enteropathogenic Escherichia coli by using a positive-selection suicide vector. Infect. Immun. 59: 4310-4317, 1991. PubMed: 1937792 Blomfield IC, et al. Allelic exchange in Escherichia coli using the Bacillus subtilis sacB gene and a temperature-sensitive pSC101 replicon. Mol. Microbiol. 5: 1447-1457, 1991. PubMed: 1686293 Kolter R, et al. Trans-complementation-dependent replication of a low molecular weight origin fragment from plasmid R6K. Cell 15: 1199-1208, 1978. PubMed: 728998 McIver KS, et al. The elastase propeptide functions as an intramolecular chaperone required for elastase activity and secretion in Pseudomonas aeruginosa. Mol. Microbiol. 18: 877-889, 1995. PubMed: 8825092 |
| Shipped： | frozen |
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| 产品名称： | pRE107 plasmid in E. coli |
|---|---|
| 商品货号： | TS204663 |
| Designations： | pRE107 plasmid in E. coli |
| Depositors： | DM Schifferli, University of Pennsylvania School of Veterinary Medicine, Philadelphia, PA |
| Biosafety Level： | 1 |
| Host： | Escherichia coli SM10 lambda pir |
| Vector Information： | Size (kb): 6.55
Vector: pRE107 (plasmid)
Construction: pGP704, sacB1 (pUC58)
Marker(s): ampR,sacB
Construct size (kb): 6.55
Features: marker(s): ampR marker(s): sacB1 replicon: conditional R6K ori replicon: oriT MCS: PstI...EcoRI restriction site: EcoRI HindIII |
| Applications： | Counterselection levansucrase Suicide vector Vector permitting allelic exchange of cloned inserts |
| Comments： | Restriction digests of the clone give the following sizes (kb): BamHI-- 3.2, 1.7, 1.5; XbaI-- 6.55; EcoRI-- 4.0, 2.8. The sacB1 allele is a variant of sacB with certain restriction sites removed by site directed mutagenesis. Expression of sacB confers sensitivity to sucrose. The conditional R6K origin of replication requires that the pi protein be expressed in trans for plasmid maintenance. One of four allelic exchange suicide vectors (TS204663 - 87694) that provide both selection for chromosomal integration (ampR, cmlR, kanR or tetR) and counterselection for loss of vector DNA and the wild type allele. Construct is suicide plasmid in any host not expressing pir. Cloned inserts may be integrated into the host chromosome (a single recombination event) following electroporation and appropriate antibiotic selection. Negative selection for sucrose sensitivity (sacB) selects for a second recombination event resulting in loss of vector DNA. |
| Media： | ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin |
| Growth Conditions： | Temperature: 37°C |
| References： | Chang TW, et al. Immunoassay for biologically active human interferon-gamma employing unique monoclonal antibodies. US Patent 4,666,865 dated May 19 1987 Edwards RA, et al. Improved allelic exchange vectors and their use to analyze 987P fimbria gene expression. Gene 207: 149-157, 1998. PubMed: 9511756 Donnenberg MS, Kaper JB. Construction of an eae deletion mutant of enteropathogenic Escherichia coli by using a positive-selection suicide vector. Infect. Immun. 59: 4310-4317, 1991. PubMed: 1937792 Blomfield IC, et al. Allelic exchange in Escherichia coli using the Bacillus subtilis sacB gene and a temperature-sensitive pSC101 replicon. Mol. Microbiol. 5: 1447-1457, 1991. PubMed: 1686293 Kolter R, et al. Trans-complementation-dependent replication of a low molecular weight origin fragment from plasmid R6K. Cell 15: 1199-1208, 1978. PubMed: 728998 McIver KS, et al. The elastase propeptide functions as an intramolecular chaperone required for elastase activity and secretion in Pseudomonas aeruginosa. Mol. Microbiol. 18: 877-889, 1995. PubMed: 8825092 |
| Shipped： | frozen |
