Protocol tips
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Protocol tips |
Downstream tips |
Phusion Hot Start II DNA Polymerase tends to work better at elevated denaturation and annealing temperatures due to higher salt concentrations in its buffer. Hence follow manufacturer instruction strictly. |
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Upstream tips |
Phusion Hot Start II DNA Polymerase tends to work better at elevated denaturation and annealing temperatures due to higher salt concentrations in its buffer. Hence follow manufacturer instruction strictly. |
Publication protocol
Cloning of Human MDR3 and Site-directed Mutagenesis
We cloned human wild type MDR3 (NM_000443.3) as described previously (18). Site-directed mutagenesis was carried out with the QuikChange® XL (Agilent Technologies) and the Phusion site-directed mutagenesis kit (Thermo Scientific), respectively. To generate the ATPase-deficient mutant, we exchanged Glu-558 and Glu-1207 of the conserved Walker B motif against Gln with the primer pair as described before (18). The Q1174E mutant was introduced into MDR3 with the Phusion site-directed mutagenesis kit (Thermo Scientific) using forward primer 5′-GATAAGGGGACTGAGCTCTCAGGAGGTCAAAAAC-3′ and the reverse primer 5′-CCCACTCTTGTTTCATATTTGTGGGGTAACG-3′. The sequences of all constructs were verified by DNA sequencing (GATC Biotech).
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Papers
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Paper title
A Mutation within the Extended X Loop Abolished Substrate-induced ATPase Activity of the Human Liver ATP-binding Cassette (ABC) Transporter MDR3
Manufacturer protocol
Download the product protocol from Thermo Fisher Scientific for Phusion Site-Directed Mutagenesis Kit below.
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