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Found 5 matching solutions for this experiment
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Digestion reactions were set up in 12 μl volume using 96 fmoles of duplex per reaction, with SUPERase•In™ RNase Inhibitor 1 U/μl, in the buffer recommended by the manufacturer. Enzymes were used at a maximum concentration compatible with glycerol content lower than 4.75%. MvaI, HindIII, PvuII (Fastdigest™ series) and BcnI enzymes were from Thermo Scientific™. AvaII, HinP1I and EcoRV were from New England Biolabs. |
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Digestion reactions were set up in 12 μl volume using 96 fmoles of duplex per reaction, with SUPERase•In™ RNase Inhibitor 1 U/μl, in the buffer recommended by the manufacturer. Enzymes were used at a maximum concentration compatible with glycerol content lower than 4.75%. MvaI, HindIII, PvuII (Fastdigest™ series) and BcnI enzymes were from Thermo Scientific™. AvaII, HinP1I and EcoRV were from New England Biolabs. |
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The clone 4G4E4.0 encompassing a 4-kb EcoRI 59 fragment of the human huntingtin gene (including exon 1 and upstream noncoding region) (Lin et al.,
1995) was characterized by restriction endonuclease mapping with EcoRI, HindIII, and SfiI. A region of 3345 nt of the 59-untranslated region was deleted by double digestion with HindIII and SfiI to form a human huntingtin exon 1 transcription plasmid (clone 839; Fig. 1).
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The clone 4G4E4.0 encompassing a 4-kb EcoRI 59 fragment of the human huntingtin gene (including exon 1 and upstream noncoding region) (Lin et al.,
1995) was characterized by restriction endonuclease mapping with EcoRI, HindIII, and SfiI. A region of 3345 nt of the 59-untranslated region was deleted by double digestion with HindIII and SfiI to form a human huntingtin exon 1 transcription plasmid (clone 839; Fig. 1).
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The plasmid DNA of pBS3ndd was isolated using the alkaline lysis method, then linearized by digestion with EcoRI-HF and HindIII-HF for 3 h. Cut vector was precipitated with two volumes of absolute ethanol, incubated at −80 °C for 1 h, and then harvested by centrifugation at 16,000×g at room temperature for 10 min. The DNA pellet was rinsed once with 70% ethanol, air-dried, and resuspended with TE buffer. |
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The plasmid DNA of pBS3ndd was isolated using the alkaline lysis method, then linearized by digestion with EcoRI-HF and HindIII-HF for 3 h. Cut vector was precipitated with two volumes of absolute ethanol, incubated at −80 °C for 1 h, and then harvested by centrifugation at 16,000×g at room temperature for 10 min. The DNA pellet was rinsed once with 70% ethanol, air-dried, and resuspended with TE buffer. |
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The DNA fragments of the PCR were purified with the QIAquick PCR purification kit (Qiagen, Inc., Valencia, CA) and afterward digested with HindIII and BamHI (New England Biolabs, Beverly, MA). |
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The DNA fragments of the PCR were purified with the QIAquick PCR purification kit (Qiagen, Inc., Valencia, CA) and afterward digested with HindIII and BamHI (New England Biolabs, Beverly, MA). |
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After digested with BamHI and HindIII (Takara), the PCR products were cloned into expression vector, pET-32a(+) (Novagen). |
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After digested with BamHI and HindIII (Takara), the PCR products were cloned into expression vector, pET-32a(+) (Novagen). |
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