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Turbo dna free dnase

Manufactured by Promega

TURBO DNA-free™ DNase is a recombinant DNase I enzyme designed for rapid and efficient removal of DNA from RNA samples. The enzyme is highly active and heat-inactivated, allowing for easy removal of residual DNA without affecting the RNA.

Automatically generated - may contain errors

2 protocols using turbo dna free dnase

1

Hepatic RNA Extraction and Quantification

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Total RNA was extracted from frozen livers using ReliaPrep™ RNA Tissue Miniprep System (Promega), according to the manufacturer’s instructions, as described63 (link), genomic DNA contamination was removed using Ambion® TURBO DNA-freeTM DNase. 1 μg of total RNA was reverse transcribed with Superscript IV Vilo (Life Technologies) prior to qPCR analysis for mouse il2 (TaqMan Mm00434256, Life Technologies), ifng (TaqMan Mm01168134, Life Technologies), HBV core (forward TACCGCCTCAGCTCTGTATC, reverse CTTCCAAATTAACACCCACCC, probe TCACCTCACCATACTGCACTCAGGCAA). Reactions were run and analysed on Quant Studio 5 instrument (Life Technologies). For viremia quantification, a standard curve was drawn using plasmid DNA. All experiments were performed in triplicate and normalized to the reference gene GAPDH.
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2

Hepatic RNA Extraction and Quantification

Check if the same lab product or an alternative is used in the 5 most similar protocols
Total RNA was extracted from frozen livers using ReliaPrep™ RNA Tissue Miniprep System (Promega), according to the manufacturer’s instructions, as described63 (link), genomic DNA contamination was removed using Ambion® TURBO DNA-freeTM DNase. 1 μg of total RNA was reverse transcribed with Superscript IV Vilo (Life Technologies) prior to qPCR analysis for mouse il2 (TaqMan Mm00434256, Life Technologies), ifng (TaqMan Mm01168134, Life Technologies), HBV core (forward TACCGCCTCAGCTCTGTATC, reverse CTTCCAAATTAACACCCACCC, probe TCACCTCACCATACTGCACTCAGGCAA). Reactions were run and analysed on Quant Studio 5 instrument (Life Technologies). For viremia quantification, a standard curve was drawn using plasmid DNA. All experiments were performed in triplicate and normalized to the reference gene GAPDH.
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