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Perfect for antibody phage display or peptide phage display library creation
(1987) Nucleic Acids Res
alcohol or other buffers required
since any contaminating DNA would also be a template for random-primed cDNA synthesis
PCR-ready DNA in under 20 mins
Baseline-ZERO-DNase, 5,000 U size:EACH Perfect for antibody phage displayEffectively digest large or small dsDNA and ssDNA into mononucleotides Digest unwanted dsDNA and ssDNA molecules including small ssDNA such as random hexamers Use in sensitive applications requiring reverse transcription where any contaminating DNA is unwanted Applications Removal of genomic DNA from small sample total RNA preparations for expression analysis (Fig. 1) Removal of small DNA oligonucleotides (e. g., random primers) Baseline ZERO DNase*
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