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Rnaiso plus

Manufactured by Transgene
Sourced in China

RNAiso Plus is a reagent used for the isolation and purification of total RNA from various biological samples. It is a ready-to-use solution that effectively extracts RNA while maintaining its integrity and purity.

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3 protocols using rnaiso plus

1

Quantitative RT-PCR Analysis of Extracellular Matrix Genes

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Total RNA from HSC-T6 cells was extracted using RNAiso Plus (Transgen Biotech, Beijing, China) following the manufacturer’s protocol, and the purity of the extracted RNA was determined. The primers of COL3A1 [collagen type III alpha 1 chain], COL1A1 (collagen type I alpha 1 chain), α-SMA (α-smooth muscle actin), SDC-4 (syndecan-4), and GAPDH are listed in Table 1. cDNA was synthesized using a PrimeScript® RT reagent kit according to the manufacturer’s instructions (Transgen Biotech, Beijing, China). For real-time PCR assay, SYBR® Premix Ex TaqTM II (Transgen Biotech, Beijing, China) was used and subjected to quantitative PCR in an ABI 7500 Real Time PCR System, and the data was analyzed using System SDS software (Applied Biosystems, United States).
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2

Lily Petal Total RNA Extraction

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Total RNA was extracted from the lily petals at FS using RNAiso Plus (TransGen Biotech, Beijing, China). The quality and quantity of purified RNA were examined using a NanoDrop ND-1000 UV/Visible spectrophotometer (Wilmington, DE, USA). The RIN (RNA integrity number) values (>8.0) of these samples were assessed using an Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA) for gel electrophoresis. High-quality RNA was used in cDNA library construction and Illumina deep sequencing.
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3

Liver qPCR Gene Expression Analysis

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qPCR was performed to validate gene expressions in liver tissue. RNA was extracted from the liver by using RNAiso Plus (TransGen Biotech, Beijing, China). Total RNA was reverse transcribed into cDNA with oligo (dR) primers by using TransScript All-in-One First-Strand cDNA Synthesis SuperMix (TransGen Biotech). qPCR were performed using the TransStart Top Green qPCRSuperMix (TransGen Biotech) and subjected to CFX96 PCR system (Bio-Rad Laboratories, Hercules, CA, USA). The levels of gene were normalized to those of β-actin and gene expressions were analyzed by 2−ΔΔCt method. Each experiment was performed once with three technical triplicates per sample.
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