pSKI074植物激活标记技术activation tagging载体-BioVector NTCC质粒载体菌种细胞蛋白抗体基因保藏中心
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- 货 号:pSKI074植物激活标记技术activation tagging载体
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pSKI074植物激活标记技术activation tagging载体
Map图谱
The CaMV 35S enhancers in these vectors correspond to nucleotides -417 to -86 relative to the transcription start.
Recommended Agrobacterium strain is GV3101 pMP90RK. Host and helper plasmid markers are kanamycin, gentamycin and rifampicin resistance.
Plasmid selection in E. coli and in A. tumefaciens is ampicillin resistance.
Sites that leave the pBstKS+ sequences intact and cut only on one side between pBstKS+ and either left or right border can be used for plasmid rescue. Note that there are additional BssS1 sites not shown on the map.
The four enhancer repeats in the construct may be unstable in E. coli and Agrobacterium if stored at +4'C for extended time. Check by PCR with T7 (or M13-20) oligo and this one derived from the RB sequence: 5' acc cgc caa tat atc ctg 3'. This should give 1.4 kb band. Note that these oligos will not work in a transgenic plant, as the RB sequence is not transfered. Using this test, we found that after 1-2 weeks in a fridge the Agrobacterium strain loses on average one copy of a repeat, and after a month in a fridge there is only one copy left. It is a good idea to use a freshly streaked colony from a good -70'C glycerol stock for every infiltration.
- Vector backbonepPCVICEn4HPT(Search Vector Database)
- Backbone manufacturerHayashi et al, 1992
Backbone size w/o insert (bp)10138
- Vector typePlant Expression ; Activation tagging
- Selectable markerskanamycin
GROWTH IN BACTERIA
- Bacterial Resistance(s)Ampicillin
- Growth Temperature37°C
- Growth Strain(s)DH5alpha
- Growth instructionsPlasmid grow in standard E. coli at 37 degrees, but the four enhancer repeats may be unstable in E. coli and A. tumefaciens if stored at 4'C for extended time. See comments.
- Copy numberHigh Copy
GENE/INSERT
- Gene/Insert nameCaMV 35S enhancers
- SpeciesCauliflower mosaic virus
- GenBank IDAF218466
CLONING INFORMATION
Cloning methodRestriction Enzyme
5′ cloning siteSee map and paper. (not destroyed)
3′ cloning siteSee map and paper. (not destroyed)
5′ sequencing primerT7
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