Biology Reference
In-Depth Information
Fig. 1 Overview of strategy to produce capsid modifi ed adenoviral vectors
Ultimately, these vectors should enable the production of safer,
more effi cacious vectors for in vivo applications whose tropism can
be tailored towards individual applications.
2
Materials
2.1 Generation of
Adenoviral Vectors
with Altered Penton
Base and Hexon
Proteins
1. Proof Reading Taq polymerase (Herculase II Fusion DNA
Polymerase, #600677-41, Stratagene, CA, USA).
2. Rapid DNA Ligation kit (#11635379001, Roche, Mannheim,
Germany).
3. StrataClone Blunt PCR cloning kit (Stratagene, #240207, CA,
USA).
4. Annealing buffer: 10 mM Tris-HCl, pH 7.5-8.0, 60 mM
NaCl, 1 mM EDTA.
5. DH5
2.1.1 General Molecular
Biology Reagents
TOP10 competent bacteria.
6. 1 kB and 100 bp molecular weight ladders.
α
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