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Sybr qpcr kit

Manufactured by Roche
Sourced in United States

The SYBR® qPCR kit is a reagent system designed for quantitative real-time PCR (qPCR) analysis. The kit contains SYBR® Green I dye, which binds to double-stranded DNA and emits a fluorescent signal proportional to the amount of amplified DNA. This allows for the real-time monitoring and quantification of DNA targets during the PCR process.

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2 protocols using sybr qpcr kit

1

RNA Extraction and qPCR Analysis of Cytokine Gene Expression in hCASMCs

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Total RNA was extracted from hCASMCs using an RNeasy Protect Cell Mini Kit (Qiagen, Hilden, Germany), according to the manufacturer's protocol, as described previously 1, 20, 21, 22, 23, 24. After quantifying the isolated RNA using a spectrophotometer, 0.5‐μg aliquots were reverse‐transcribed using a High‐Capacity cDNA Reverse Transcription Kit (Applied Biosystems, Foster City, CA, USA). PCR primers were obtained from Nihon Gene Research Laboratories (Sendai, Japan). The primer sequences used to amplify IL‐6, EREG, and AREG mRNA are shown in Table 1. The real‐time PCR assay was carried out using a SYBR® qPCR kit (KAPA Biosystems, Woburn, MA, USA) in a Thermal Cycler Dice (TaKaRa, Kusatsu, Japan). The mRNA expression level was normalized to that of β‐actin.
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2

Gene Expression Analysis by qPCR

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Total RNA was extracted from cells with RNeasy kit (Qiagen) according to the manufacturer's instruction. Complementary DNA (cDNA) was synthesized with Superscript reverse transcriptase (Invitrogen). Gene expressions were measured by 7500 real-time PCR system (Applied Biosystems) with SYBR qPCR kit (KAPA). Actinb, Gapdh, or Rn18S was used as internal control. The primer sequences are available upon request.
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