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Rnaiso trizol reagent

Manufactured by Takara Bio
Sourced in Japan

RNAiso TRIzol reagent is a monophasic solution of phenol and guanidine isothiocyanate designed for the isolation of total RNA from various biological samples. It is a reagent used for the extraction and purification of RNA.

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4 protocols using rnaiso trizol reagent

1

Quantitative RT-PCR Analysis of Gene Expression

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Total RNA was isolated using RNAiso TRIzol reagent (Takara) and reverse transcribed with PrimeScript RT Master Mix (Takara) according to the manufacturer's instructions. Then, SYBR Fast qPCR Mix (Takara) in a Bio‐Rad CFX96 Real‐Time PCR Detection System (Bio‐Rad) was used for qRT‐PCR. qRT‐PCR was performed in triplicate, and the results were normalized against GAPDH.
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2

Quantitative RT-PCR Analysis of Gene Expression

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Total RNA was isolated using RNAiso TRIzol reagent (Takara), and reverse-transcribed with PrimeScript RT Master Mix (Takara) according to the manufacturer’s instructions. Then a SYBR Fast qPCR Mix (Takara) in a Bio-Rad CFX96 Real-Time PCR Detection System (Bio-Rad) was used for qRT-PCR. qRT-PCR was performed in triplicate and the results were normalized against β-actin. The sequences of all primers for qRT-PCR are listed in Supplementary Table S1.
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3

Quantitative Gene Expression Analysis

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Total RNA was extracted using RNAiso Trizol reagent (Takara, Kyoto, Japan), PrimeScript™ RT Master Mix (Takara, Japan) was used for reverse transcription according to the manufacturer's instructions. cDNA was amplified and quantified by Applied Biosystems 7500 (Thermo Fisher, USA) using SYBR Green (TaKaRa, Japan). GAPDH was used as internal controls, Primers were synthesized and purified by RiboBio (Guangzhou, China) and the primers are listed in Additional file 5: Table S5. The fold changes were determined using the relative quantification 2-△△CT method.
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4

Quantitative RT-PCR for FPR2 Gene Expression

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Total RNA was isolated using RNAiso TRIzol reagent (TAKARA, Kyoto, Japan) according to the manufacturer’s instructions. Reverse-transcription of RNA was performed in a final reaction volume of 20 μL containing 1000 ng of total RNA by using PrimeScript RT Master Mix (TAKARA, Kyoto, Japan). FPR2 mRNAs were detected by qRT-PCR with the SYBR Premix Ex TaqII (TAKARA, Kyoto, Japan). The sequences of all primers for RT-qPCR were presented in Table S2.
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