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Quanta Biosciences
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highQu Inc
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Bio-Rad
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Promega
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Avantor
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Promega
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Quanta Biosciences
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Becton Dickinson
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Biolegio bv
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LI-COR
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LI-COR
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JN Medsys
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Image Search Results
Journal: Scientific Reports
Article Title: NAxtra magnetic nanoparticles for low-cost, efficient isolation of mammalian DNA and RNA
doi: 10.1038/s41598-023-46868-5
Figure Lengend Snippet: Nucleic acid (NA) extraction from 100 to 1,000,000 cells (HAP1), comparing the NAxtra-based method on KingFisher Flex (three independent NA extractions) to the AllPrep DNA/RNA/miRNA Universal Kit (two independent NA extractions). (A) NAs extracted from 1 = 1,000,000 and 2 = 500,000 cells, separated on a 0.4% agarose gel (left, 1% eluate applied for 1,000,000 cells, 2% eluate applied for 500,000 cells) with GeneRuler High Range DNA ladder (Thermo Scientific), or 1.2% agarose gel (right, 4% eluate applied for 1,000,000 cells, 8% eluate applied for 500,000 cells) with GeneRuler 1 kb Plus DNA Ladder (Thermo Scientific). Gel images have been inverted and cropped; original gels are presented in Supplementary Fig. . ( B ) Average NA yields (± 1 SD) from 500,000 and 1,000,000 cells, as measured by Quant-iT RNA/DNA assay (Invitrogen). ( C ) Average cycle threshold (Ct) values (± 1 SD) for DNA target (left; a 305 bp, single-locus genomic DNA amplicon from the KAPA Human Genomic DNA Quantification and QC Kit) and RNA target (right; ACTB) amplified by (RT-)qPCR of NA extracted from 100; 1000; 10,000 and 100,000 cells.
Article Snippet: ACTB mRNA was reverse transcribed and amplified in reactions of 2.5 μl template RNA, 1X ACTB PrimeTime XL PCR Assay Hs.PT.39a.22214747 (Integrated DNA Technologies), and either 1X qScript XLT 1-Step RT-qPCR ToughMix (Quantabio), 1X One-Step Takyon Ultra Probe 4X MasterMix (Eurogentec), or
Techniques: Extraction, Agarose Gel Electrophoresis, Amplification, Quantitative RT-PCR
Journal: Scientific Reports
Article Title: NAxtra magnetic nanoparticles for low-cost, efficient isolation of mammalian DNA and RNA
doi: 10.1038/s41598-023-46868-5
Figure Lengend Snippet: Nucleic acids (NA) extracted from adherent cells (HAP1) using the NAxtra-based method on KingFisher Flex (three independent NA extractions) compared to the AllPrep DNA/RNA/miRNA Universal Kit (two independent NA extractions). Average cycle threshold (Ct) values (± 1 SD) for a DNA target (top, MYC) and RNA target (bottom, ACTB) amplified by (RT-)qPCR of NAs extracted from 100 cells and 100,000 cells of HAP1. Two different master mixes were used for each target: RealQ Plus 2 × Master Mix for Probe (Ampliqon) and Luna Universal Probe qPCR Master Mix (NEB), or One-Step Takyon Ultra Probe 4X MasterMix (Eurogentec) and 4X 1Step RT qPCR Probe Kit (highQu).
Article Snippet: ACTB mRNA was reverse transcribed and amplified in reactions of 2.5 μl template RNA, 1X ACTB PrimeTime XL PCR Assay Hs.PT.39a.22214747 (Integrated DNA Technologies), and either 1X qScript XLT 1-Step RT-qPCR ToughMix (Quantabio), 1X One-Step Takyon Ultra Probe 4X MasterMix (Eurogentec), or
Techniques: Amplification, Quantitative RT-PCR
Journal: Scientific Reports
Article Title: NAxtra magnetic nanoparticles for low-cost, efficient isolation of mammalian DNA and RNA
doi: 10.1038/s41598-023-46868-5
Figure Lengend Snippet: RNA isolated from triplicates of 1,000,000 cells (HAP1) using the NAxtra-based method compared to the MagMAX mir Vana Total RNA isolation kit (Applied Biosystems) on KingFisher Duo Prime. Statistical analysis was performed by two-sided, unpaired t-tests, in which ns (non-significant) = P > 0.05, * = P ≤ 0.05, ** = P ≤ 0.01, and **** P ≤ 0.0001. ( A ) Total RNA separated on a 1.2% agarose gel (5% eluate applied) with GeneRuler 1 kb Plus DNA Ladder (Thermo Scientific). The gel image has been inverted and cropped; the original gel is presented in Supplementary Fig. . ( B ) Average total RNA yield (± 1 SD), as measured by Quant-iT RNA assay (Invitrogen) ( C ) Average cycle threshold (Ct) values (± 1 SD) for five miRNA targets; hsa-miR-24-3p, hsa-miR-122-5p, hsa-miR-210-5p, hsa-miR-455-5p and hsa-miR-1246, amplified by RT-qPCR. D) Average cycle threshold (Ct) values (± 1 SD) for an mRNA target (ACTB) amplified by RT-qPCR.
Article Snippet: ACTB mRNA was reverse transcribed and amplified in reactions of 2.5 μl template RNA, 1X ACTB PrimeTime XL PCR Assay Hs.PT.39a.22214747 (Integrated DNA Technologies), and either 1X qScript XLT 1-Step RT-qPCR ToughMix (Quantabio), 1X One-Step Takyon Ultra Probe 4X MasterMix (Eurogentec), or
Techniques: Isolation, Agarose Gel Electrophoresis, Amplification, Quantitative RT-PCR