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Cdna synthesis kit

Manufactured by EURx
Sourced in Poland

The cDNA Synthesis Kit is a laboratory tool used to convert RNA into complementary DNA (cDNA) molecules. This process involves the reverse transcription of RNA templates into single-stranded cDNA, which can then be used for various downstream applications such as gene expression analysis, cloning, and sequencing.

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3 protocols using cdna synthesis kit

1

Quantitative Gene Expression Analysis of Spinal Cord Injury

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Total RNA was extracted from injured spinal cord tissues using Universal DNA/ RNA/Protein Purification kit (EURx, Poland), then RNA concentrations were determined using the nanodropper; cDNA was synthesized from isolated RNA via cDNA synthesis kit (EURx,E0801-02, Poland). Amplification and real-time detection were performed on an ABI model Stepone (Thermo fisher scientific, USA) using SG qPCR Master mix (EURx, E0402-01, Poland) and QuantiTect primers (Cinna Gen, Iran). The improved four-step reaction was used: 95 °C 10 min; 95 °C 10s, 60 °C 30 s, 72 °C 30 s, and 85 °C 15 s, for 40 cycles; the melting curve analysis was done with the temperature ranging from 60 to 95 °C, gradually increasing at a speed of 0.5 °C every 10 s. Relative quantitative analysis of the final results was normalized to beta-actin (Table 2).

Sequence of primer pairs for real-time PCR

Primer nameSequence 5′-3′
IL-6 (forward)GACTGATGTTGTTGACAGCC
IL-6 (reverse)CTGACAGTGCATCATCGCTG
BDNF (forward)GGCTGACACTTTGAGCACG
BDNF (reverse)GCTGTGACCCACTCGCTAA
GDNF (forward)TATGGGATGTCGTGGCTGTC
GDNF (reverse)CGCCGCTTGTTTATCTGGTG
Beta-actin (forward)GGCAAGGTCATCCCAGAGC
Beta-actin (reverse)CATCATACTTGGCAGGTTTCTCC

IL-6 interlukin6, BDNF brain-derived neurotrophic factor, GDNF glial cell line-derived neurotrophic factor

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2

RNA Extraction and cDNA Synthesis

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Total RNA extraction was extracted from MC4-L2 cell line-treated and tumor tissues of mice using TRIZOL reagent (Gene All, South Korea), according to the manufacturer's instructions. RNA concentrations were determined using the NanoDrop spectrophotometer (Thermo Scienti c, Germany). The quality of extracted RNA was assessed by 1% agarose gel electrophoresis. After RNA extraction, the complementary DNA (cDNAs) were synthesized using a cDNA synthesis kit (EURx, Poland), according to the manufacturer's instructions.
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3

Total RNA Extraction and cDNA Synthesis

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Total RNA extraction was extracted from MC4-L2 cell line treated and tumor tissues of mice using TRIZOL reagent (Gene All, South Korea), according to the manufacturer's instructions. RNA concentrations were determined using the NanoDrop spectrophotometer (Thermo Scienti c, Germany). The quality of extracted RNA was assessed by 1% agarose gel electrophoresis. After RNA extraction, the complementary DNA (cDNAs) were synthesized using a cDNA synthesis kit (EURx, Poland), according to the manufacturer's instructions.
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