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Superscript 2 reverse transcriptase for qpcr

Manufactured by Thermo Fisher Scientific

SuperScript II Reverse Transcriptase is a recombinant reverse transcriptase enzyme used for the conversion of RNA to cDNA for quantitative PCR (qPCR) applications. It has been engineered for improved thermal stability and reduced RNase H activity.

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2 protocols using superscript 2 reverse transcriptase for qpcr

1

Quantitative Gene Expression Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Total cellular RNAs were extracted using QIAGEN RNeasy Mini Kit (# 74104) according to the manufacturer’s instructions, and RNA purity was confirmed by analysis of the ratio of absorbance at 260 nm to that at 280 nm absorption. cDNAs were prepared from 1 g total RNAs using SuperScript II Reverse Transcriptase for qPCR (Invitrogen, #18064022) according to the manufacturer’s instructions. qRT-PCR was performed using SYBR Green PCR Master Mix (Applied Biosystems, # 4344463) and QuantiTect Primer (QIAGEN) in an ABI PRISM 7900 Sequence Detection System (Applied Biosystems). Relative mRNA expression was calculated using the comparative Ct method after normalization to a loading control. Samples were run in triplicates with a primer-limited probe for the reference gene. Primers are provided in Key Resources Table.
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2

Quantitative Gene Expression Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Total cellular RNAs were extracted using QIAGEN RNeasy Mini Kit (# 74104) according to the manufacturer’s instructions, and RNA purity was confirmed by analysis of the ratio of absorbance at 260 nm to that at 280 nm absorption. cDNAs were prepared from 1 g total RNAs using SuperScript II Reverse Transcriptase for qPCR (Invitrogen, #18064022) according to the manufacturer’s instructions. qRT-PCR was performed using SYBR Green PCR Master Mix (Applied Biosystems, # 4344463) and QuantiTect Primer (QIAGEN) in an ABI PRISM 7900 Sequence Detection System (Applied Biosystems). Relative mRNA expression was calculated using the comparative Ct method after normalization to a loading control. Samples were run in triplicates with a primer-limited probe for the reference gene. Primers are provided in Key Resources Table.
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