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In some cases, following cloning, inserts are lost due to vector-driven expression of deleterious genes, vector instability following insert driven transcription and finally inappropriate antibiotic resistance.
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A great management package, including remote manageability, and a case design that allows you to remove and insert drives without using tools are attractive features.
Insert drives into their slots carefully, in right position, and at the correct angle.
Insert drives into their slots carefully and at the correct angle.
In addition, the long terminal repeats (LTRs) were removed and transcription of the VLP insert was driven by the addition of the cytomegalovirus immediate-early (CMV-IE) promoter.
Transcription of each insert was driven by the CMV promoter.
Using a moving phantom (Modus Medical Quasar, London, ON, Canada) the Perspex insert was driven forward and back 40 mm in one direction to simulate respiratory motion.
After drilling the defect to the required depth, an extractor was inserted and driven down to the bottom of the defect.
This plasmid contained a T7 RNA polymerase promoter upstream of the insert to drive transcription by this enzyme.
The ulnar nerve is not at risk, unless the proximally inserted wire is driven through the medial condyle.
Transcription of the inserted sequences was driven by the immediate-early promoter of human cytomegalovirus in these vectors.
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