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Rna purification kit

Manufactured by Vazyme
Sourced in China

The RNA Purification Kit is a laboratory equipment designed to extract and purify RNA from various biological samples. It utilizes a column-based method to efficiently capture and concentrate RNA, while removing contaminants and inhibitors. The kit provides a streamlined workflow for obtaining high-quality RNA suitable for downstream applications, such as RT-PCR, RNA sequencing, and gene expression analysis.

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2 protocols using rna purification kit

1

RNA Extraction and qRT-PCR Analysis

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Total RNA was extracted with an RNA Purification Kit (cat #: RC101-01, Vazyme, Nanjing, China) and reverse transcription was performed with a cDNA Reverse Transcription Kit (cat #: R223-01, Vazyme, Nanjing, China). qRT-PCR was performed using SYBR Green qPCR Master Mix ((cat #: Q121-02, Vazyme, Nanjing, China). Relative gene expression was calculated using the 2−ΔΔCT method, and GAPDH was used as a reference for normalization. The qPCR primers were listed in Additional file 2: Table S1.
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2

Evaluating Epithelial-Mesenchymal Transition in HaCaT Cells

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Prior to qPCR analysis, the HaCaT cells were seeded in a 6-well plate and subjected to graded concentrations of MY-1 (0 nM, 10 nM, and 100 nM) for 24 h. The total RNA was extracted with an RNA purification kit (Vazyme, Nanjing, China) and reverse transcription was performed with a cDNA reverse transcription kit (Vazyme). qPCR was performed employing SYBR Green qPCR Master Mix (Vazyme) and the expression levels of relative genes were calculated utilizing the 2−ΔΔCT method, with GAPDH used as a reference for normalization. The qPCR primers provided by Qingke (Beijing, China) are listed in Table 1.

Sequences of primers used for the quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR)

Gene nameForward primer sequencesReverse primer sequences
E-cadherinACATACACTCTCTTCTCTCGTCATTCTGATCGGTTAC
N-cadherinATCATCCTGCTTATCCTTTTATCTCTTACATCATCTTCTG
VimentinAACCTGAGGGAAACTAATTTGATAACCTGTCCATCT
Snail1CGCTCTTTCCTCGTCAGGTGGAAGGTAAACTCTGGATTAGA
GAPDHGGTAGTGGCGATGGCGGCTGTAGGAACGCCGACTGC
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