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Ez rna 2 isolation kit

Manufactured by Sartorius
Sourced in Israel

The EZ-RNA II isolation kit is a tool designed for the extraction and purification of RNA from various biological samples. It provides a streamlined and efficient process to isolate high-quality RNA for downstream applications.

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4 protocols using ez rna 2 isolation kit

1

Total RNA Extraction for miRNA Analysis

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Total RNA was extracted 3 days post infection using EZ-RNA II isolation kit (Biological Industries, Beit Haemek, Israel), according to the manufacturer’s protocol. Aliquots of total RNA were used directly for miRNAs quantification using qPCR or subjected to small RNA library construction.
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2

Total RNA and Exosomal RNA Isolation

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Total RNA was extracted using the EZ-RNA II Isolation Kit reagent (Biological Industries Beit Haemek, Israel) according to manufacturer's instructions. Briefly, cells were lysed with guanidine thiocyanate detergent solution, followed by organic extraction and alcohol precipitation of the RNA. Quantification and the purity of total RNA were assessed by using the NanoDrop1000® spectrophotometer (Thermo Fisher Scientific, MA, USA).
RNA isolation from exosomes was performed by using Total Exosome RNA and Protein Isolation Kit (Invitrogen, CA, USA). Exosomes were lysed with denaturing solution and then precipitated by acid-phenol: chloroform solution followed by several washes and centrifugation steps. The supernatant was then placed on filter cartridge tubes for further purification using numerous washing solutions provided by the kit. RNA was eluted with PCR grade water.
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3

Comprehensive Cellular RNA Extraction

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RNA extraction from cells was performed using the EZ-RNA II Isolation Kit (Biological Industries Beit Haemek, Israel) according to the manufacturer's instructions. Extracted RNA was quantified by the NanoDrop spectrophotometer with ND-1000 software (Thermo scientific, MA, USA). The RNA extraction from exosomes was executed using the Total Exosome RNA and Protein Isolation Kit (Invitrogen, CA, USA) according to manufacturer's instructions.
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4

Evaluating Cytokine Response in PBMC Cells

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Peripheral blood mononuclear cells (PBMCs) were incubated with dPG-NH2, miR-34a and dPG-NH2–miR-34a for 4 h at 37 °C. Lipopolysacharides (Sigma) were used as positive control (1 μg/mL), PBS as negative control. Upon incubation, RNA was isolated from cell pellets and reverse transcribed using EZ-RNA II isolation kit and EZ-first strand cDNA synthesis kit (Biological industries). TNF-α and IL-6 levels were assessed by SYBR green based real-time PCR and normalized to GAPDH (primers in Supplementary Material).
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