nanodrop 1000 Thermo Fisher Search Results


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  • 99
    Thermo Fisher thermo fisher nanodrop na 1000
    Thermo Fisher Nanodrop Na 1000, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 18 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher nanopdrop 1000 spectrophotometer
    Nanopdrop 1000 Spectrophotometer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 61 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher nanodroph nd 1000 spectrophotometer
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    Thermo Fisher nanodropã‚â nd 1000 spectrophotometer
    Nanodropã‚â Nd 1000 Spectrophotometer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 91/100, based on 13 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher nanodropr nd 1000 spectrophotometer
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    Thermo Fisher nanodrop spectrophotometer nd 1000
    Scatter diagrams showing the quantity and quality of DNA in blood and milk. DNA samples were obtained from 2 BLV-negative cattle in Farm 3, 43 BLV-infected cattle without lymphoma in Farms 2–6, and 3 BLV-infected cattle with lymphoma in Farm 1. A The average quantities of genomic DNA in blood and milk samples were 7.9 µg and 6.7 µg, respectively, as determined with a <t>NanoDrop</t> spectrophotometer <t>ND-1000.</t> B The average A260/A280 ratios of genomic DNA in blood and milk were 1.88 and 1.87, respectively, as determined using a NanoDrop spectrophotometer ND-1000. C The threshold cycle values of the blood and milk samples were 22.12 and 22.37, respectively, as indicated with the red bold lines.
    Nanodrop Spectrophotometer Nd 1000, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 5422 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher nd 1000 spectrophotometer nanodrop
    Effect of aRNA purity and labelled-aRNA purification . (A) Graph showing coupling efficiency (C) and 320/650 (B) values for six MCF-7 aRNA samples with different 260/280 ratios. (B) Agilent Bioanalyzer pattern of MCF-7 Cy5-labelled target using an aRNA with 260/280 ratio of 1.6. Sharp spikes represent uncoupled Cy5 dye. (C) Same as B for aRNA with 260/280 ratio of 2 and coupling efficiency near 1. (D) <t>NanoDrop</t> ® <t>ND-1000</t> Spectrophotometer absorptions at 320 and 650 nm wavelengths of a MCF-7 Cy5-labelled target. 320/650 ratio-0.6. (E) Same as in d (different sample). 320/650 ratio-0.09. (F) Recovery rates (R) and coupling efficiencies (C) for different labelled-aRNA purification methods. Data is presented for MCF-7 cell line and measurements represent an average of three separate reactions. Li-ETOH – LiCl-ethanol; PCI – phenol/chloroform/isoamyl alcohol.
    Nd 1000 Spectrophotometer Nanodrop, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 9521 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher spectrophotometric nanodrop 1000
    Effect of aRNA purity and labelled-aRNA purification . (A) Graph showing coupling efficiency (C) and 320/650 (B) values for six MCF-7 aRNA samples with different 260/280 ratios. (B) Agilent Bioanalyzer pattern of MCF-7 Cy5-labelled target using an aRNA with 260/280 ratio of 1.6. Sharp spikes represent uncoupled Cy5 dye. (C) Same as B for aRNA with 260/280 ratio of 2 and coupling efficiency near 1. (D) <t>NanoDrop</t> ® <t>ND-1000</t> Spectrophotometer absorptions at 320 and 650 nm wavelengths of a MCF-7 Cy5-labelled target. 320/650 ratio-0.6. (E) Same as in d (different sample). 320/650 ratio-0.09. (F) Recovery rates (R) and coupling efficiencies (C) for different labelled-aRNA purification methods. Data is presented for MCF-7 cell line and measurements represent an average of three separate reactions. Li-ETOH – LiCl-ethanol; PCI – phenol/chloroform/isoamyl alcohol.
    Spectrophotometric Nanodrop 1000, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 89/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher nanodrop 1000 apparatus
    Effect of aRNA purity and labelled-aRNA purification . (A) Graph showing coupling efficiency (C) and 320/650 (B) values for six MCF-7 aRNA samples with different 260/280 ratios. (B) Agilent Bioanalyzer pattern of MCF-7 Cy5-labelled target using an aRNA with 260/280 ratio of 1.6. Sharp spikes represent uncoupled Cy5 dye. (C) Same as B for aRNA with 260/280 ratio of 2 and coupling efficiency near 1. (D) <t>NanoDrop</t> ® <t>ND-1000</t> Spectrophotometer absorptions at 320 and 650 nm wavelengths of a MCF-7 Cy5-labelled target. 320/650 ratio-0.6. (E) Same as in d (different sample). 320/650 ratio-0.09. (F) Recovery rates (R) and coupling efficiencies (C) for different labelled-aRNA purification methods. Data is presented for MCF-7 cell line and measurements represent an average of three separate reactions. Li-ETOH – LiCl-ethanol; PCI – phenol/chloroform/isoamyl alcohol.
    Nanodrop 1000 Apparatus, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 137 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher nanodrop 1000 spetrophotometer
    Effect of aRNA purity and labelled-aRNA purification . (A) Graph showing coupling efficiency (C) and 320/650 (B) values for six MCF-7 aRNA samples with different 260/280 ratios. (B) Agilent Bioanalyzer pattern of MCF-7 Cy5-labelled target using an aRNA with 260/280 ratio of 1.6. Sharp spikes represent uncoupled Cy5 dye. (C) Same as B for aRNA with 260/280 ratio of 2 and coupling efficiency near 1. (D) <t>NanoDrop</t> ® <t>ND-1000</t> Spectrophotometer absorptions at 320 and 650 nm wavelengths of a MCF-7 Cy5-labelled target. 320/650 ratio-0.6. (E) Same as in d (different sample). 320/650 ratio-0.09. (F) Recovery rates (R) and coupling efficiencies (C) for different labelled-aRNA purification methods. Data is presented for MCF-7 cell line and measurements represent an average of three separate reactions. Li-ETOH – LiCl-ethanol; PCI – phenol/chloroform/isoamyl alcohol.
    Nanodrop 1000 Spetrophotometer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 84/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Correspondence between the efficiency of humic acid removal and the pH of the extraction buffer, as assessed by eye (A) and <t>NanoDrop</t> <t>ND-1000</t> spectrophotometry at 400 nm (B). Total RNA was extracted under either high-pH or low-pH conditions and was subsequently
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    Correspondence between the efficiency of humic acid removal and the pH of the extraction buffer, as assessed by eye (A) and <t>NanoDrop</t> <t>ND-1000</t> spectrophotometry at 400 nm (B). Total RNA was extracted under either high-pH or low-pH conditions and was subsequently
    Nanodrop 1000 Machine, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 80 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Correspondence between the efficiency of humic acid removal and the pH of the extraction buffer, as assessed by eye (A) and <t>NanoDrop</t> <t>ND-1000</t> spectrophotometry at 400 nm (B). Total RNA was extracted under either high-pH or low-pH conditions and was subsequently
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    Thermo Fisher nanodrop 1000 thermocycler
    Correspondence between the efficiency of humic acid removal and the pH of the extraction buffer, as assessed by eye (A) and <t>NanoDrop</t> <t>ND-1000</t> spectrophotometry at 400 nm (B). Total RNA was extracted under either high-pH or low-pH conditions and was subsequently
    Nanodrop 1000 Thermocycler, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Correspondence between the efficiency of humic acid removal and the pH of the extraction buffer, as assessed by eye (A) and <t>NanoDrop</t> <t>ND-1000</t> spectrophotometry at 400 nm (B). Total RNA was extracted under either high-pH or low-pH conditions and was subsequently
    Nano Drop Nd 1000, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 441 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Correspondence between the efficiency of humic acid removal and the pH of the extraction buffer, as assessed by eye (A) and <t>NanoDrop</t> <t>ND-1000</t> spectrophotometry at 400 nm (B). Total RNA was extracted under either high-pH or low-pH conditions and was subsequently
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    Correspondence between the efficiency of humic acid removal and the pH of the extraction buffer, as assessed by eye (A) and <t>NanoDrop</t> <t>ND-1000</t> spectrophotometry at 400 nm (B). Total RNA was extracted under either high-pH or low-pH conditions and was subsequently
    Nanodrop Nd 1000 Microspectrophotometer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 24 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Correspondence between the efficiency of humic acid removal and the pH of the extraction buffer, as assessed by eye (A) and <t>NanoDrop</t> <t>ND-1000</t> spectrophotometry at 400 nm (B). Total RNA was extracted under either high-pH or low-pH conditions and was subsequently
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    Correspondence between the efficiency of humic acid removal and the pH of the extraction buffer, as assessed by eye (A) and <t>NanoDrop</t> <t>ND-1000</t> spectrophotometry at 400 nm (B). Total RNA was extracted under either high-pH or low-pH conditions and was subsequently
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    Correspondence between the efficiency of humic acid removal and the pH of the extraction buffer, as assessed by eye (A) and <t>NanoDrop</t> <t>ND-1000</t> spectrophotometry at 400 nm (B). Total RNA was extracted under either high-pH or low-pH conditions and was subsequently
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    Correspondence between the efficiency of humic acid removal and the pH of the extraction buffer, as assessed by eye (A) and <t>NanoDrop</t> <t>ND-1000</t> spectrophotometry at 400 nm (B). Total RNA was extracted under either high-pH or low-pH conditions and was subsequently
    Nano Drop Nd 1000 System, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Correspondence between the efficiency of humic acid removal and the pH of the extraction buffer, as assessed by eye (A) and <t>NanoDrop</t> <t>ND-1000</t> spectrophotometry at 400 nm (B). Total RNA was extracted under either high-pH or low-pH conditions and was subsequently
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    Nd 1000 Spectrophotometer Analysis, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher nanodrop model 1000
    Correspondence between the efficiency of humic acid removal and the pH of the extraction buffer, as assessed by eye (A) and <t>NanoDrop</t> <t>ND-1000</t> spectrophotometry at 400 nm (B). Total RNA was extracted under either high-pH or low-pH conditions and was subsequently
    Nanodrop Model 1000, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 80/100, based on 16 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Correspondence between the efficiency of humic acid removal and the pH of the extraction buffer, as assessed by eye (A) and <t>NanoDrop</t> <t>ND-1000</t> spectrophotometry at 400 nm (B). Total RNA was extracted under either high-pH or low-pH conditions and was subsequently
    Nd 1000 Spectrophotometer System, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 79 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher nanodrop 1000 spectrophometer
    Correspondence between the efficiency of humic acid removal and the pH of the extraction buffer, as assessed by eye (A) and <t>NanoDrop</t> <t>ND-1000</t> spectrophotometry at 400 nm (B). Total RNA was extracted under either high-pH or low-pH conditions and was subsequently
    Nanodrop 1000 Spectrophometer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 93/100, based on 21 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Scatter diagrams showing the quantity and quality of DNA in blood and milk. DNA samples were obtained from 2 BLV-negative cattle in Farm 3, 43 BLV-infected cattle without lymphoma in Farms 2–6, and 3 BLV-infected cattle with lymphoma in Farm 1. A The average quantities of genomic DNA in blood and milk samples were 7.9 µg and 6.7 µg, respectively, as determined with a NanoDrop spectrophotometer ND-1000. B The average A260/A280 ratios of genomic DNA in blood and milk were 1.88 and 1.87, respectively, as determined using a NanoDrop spectrophotometer ND-1000. C The threshold cycle values of the blood and milk samples were 22.12 and 22.37, respectively, as indicated with the red bold lines.

    Journal: Veterinary Research

    Article Title: Visualizing bovine leukemia virus (BLV)-infected cells and measuring BLV proviral loads in the milk of BLV seropositive dams

    doi: 10.1186/s13567-019-0724-1

    Figure Lengend Snippet: Scatter diagrams showing the quantity and quality of DNA in blood and milk. DNA samples were obtained from 2 BLV-negative cattle in Farm 3, 43 BLV-infected cattle without lymphoma in Farms 2–6, and 3 BLV-infected cattle with lymphoma in Farm 1. A The average quantities of genomic DNA in blood and milk samples were 7.9 µg and 6.7 µg, respectively, as determined with a NanoDrop spectrophotometer ND-1000. B The average A260/A280 ratios of genomic DNA in blood and milk were 1.88 and 1.87, respectively, as determined using a NanoDrop spectrophotometer ND-1000. C The threshold cycle values of the blood and milk samples were 22.12 and 22.37, respectively, as indicated with the red bold lines.

    Article Snippet: The quantity and quality of DNA samples extracted from milk sample was determined based on the A260/280 ratio using a Nanodrop Spectrophotometer ND-1000 (Thermo Fisher Scientific).

    Techniques: Infection, Spectrophotometry

    DNA yield of dust isolated from swine confinement facilities, grain elevators and households without pets. Total genomic DNA was isolated by a bead-beating protocol (Mo Bio, Power Clean, Carlsbad, CA) and quantified using a Nanodrop ND-1000 UV spectrophotometer (NanoDrop Technologies, Wilmington, DE). Each bar represents the mean DNA yield (µg/mg dust) ± SEM from two independent dust samples.

    Journal: PLoS ONE

    Article Title: Shotgun Pyrosequencing Metagenomic Analyses of Dusts from Swine Confinement and Grain Facilities

    doi: 10.1371/journal.pone.0095578

    Figure Lengend Snippet: DNA yield of dust isolated from swine confinement facilities, grain elevators and households without pets. Total genomic DNA was isolated by a bead-beating protocol (Mo Bio, Power Clean, Carlsbad, CA) and quantified using a Nanodrop ND-1000 UV spectrophotometer (NanoDrop Technologies, Wilmington, DE). Each bar represents the mean DNA yield (µg/mg dust) ± SEM from two independent dust samples.

    Article Snippet: Total genomic DNA was isolated by bead beating following the manufacturer’s instructions (Mo Bio, PowerSoil Kit, Carlsbad, CA), then assayed using a Nanodrop ND-1000 UV spectrophotometer (NanoDrop Technologies, Wilmington, DE).

    Techniques: Isolation, Spectrophotometry

    Comparison of assembled virus genomes. (A) A Neighbour Joint tree constructed with 1000 bootstraps. NCBI reference sequences were labelled with virus names followed by the GenBank accession numbers. The Maq assembled sequences were labelled accordingly to the reference sequences used. The Sacbrood virus (SBV) reference genome was used as an outer sequence. (B) SNP profile using the 3 viral reference sequences. (C) SNP profile using the 3 Maq assembled virus genomes.

    Journal: PLoS ONE

    Article Title: Sequence Recombination and Conservation of Varroa destructor Virus-1 and Deformed Wing Virus in Field Collected Honey Bees (Apis mellifera)

    doi: 10.1371/journal.pone.0074508

    Figure Lengend Snippet: Comparison of assembled virus genomes. (A) A Neighbour Joint tree constructed with 1000 bootstraps. NCBI reference sequences were labelled with virus names followed by the GenBank accession numbers. The Maq assembled sequences were labelled accordingly to the reference sequences used. The Sacbrood virus (SBV) reference genome was used as an outer sequence. (B) SNP profile using the 3 viral reference sequences. (C) SNP profile using the 3 Maq assembled virus genomes.

    Article Snippet: Concentrations of the sRNA extracts were measured by using the Nanodrop 1000 UV-Vis spectrophotometer (Nanodrop Products, Wilmington, USA).

    Techniques: Construct, Sequencing

    Sanger sequencing validation of chimera virus. (A) Unrooted Neighbour Joint tree of the 5’ recombination junction using the sequences of RT-PCR products amplified by primers F1R1. The tree was constructed with 1000 bootstraps and scores higher than 50% were displayed. Reference sequences are labelled with the NCBI accession numbers followed by virus names. The Sanger sequences obtained in this work (NCBI Accession No: KC691296-KC691301) are labelled as F1 followed by in-house sequence IDs. (B) SNP profile of the 5’ recombination junction using the Sanger sequences, showing a decrease of polymorphism after the recombination junction. (C) Unrooted Neighbour Joint tree of the 3’ recombination junction using the sequences of RT-PCR products amplified by primers F5R5. The tree was constructed with 1000 bootstraps and scores higher than 50% are displayed. Reference sequences are labelled with the NCBI accession numbers followed by virus names. The Sanger sequences obtained in this work (GenBank Accession No: KC691302-KC691308) are labelled as F5 followed by in-house sequence IDs. (D) SNP profile of the 3’ recombination junction using the Sanger sequences, showing that nucleotide SNPs increased after the recombination junction.

    Journal: PLoS ONE

    Article Title: Sequence Recombination and Conservation of Varroa destructor Virus-1 and Deformed Wing Virus in Field Collected Honey Bees (Apis mellifera)

    doi: 10.1371/journal.pone.0074508

    Figure Lengend Snippet: Sanger sequencing validation of chimera virus. (A) Unrooted Neighbour Joint tree of the 5’ recombination junction using the sequences of RT-PCR products amplified by primers F1R1. The tree was constructed with 1000 bootstraps and scores higher than 50% were displayed. Reference sequences are labelled with the NCBI accession numbers followed by virus names. The Sanger sequences obtained in this work (NCBI Accession No: KC691296-KC691301) are labelled as F1 followed by in-house sequence IDs. (B) SNP profile of the 5’ recombination junction using the Sanger sequences, showing a decrease of polymorphism after the recombination junction. (C) Unrooted Neighbour Joint tree of the 3’ recombination junction using the sequences of RT-PCR products amplified by primers F5R5. The tree was constructed with 1000 bootstraps and scores higher than 50% are displayed. Reference sequences are labelled with the NCBI accession numbers followed by virus names. The Sanger sequences obtained in this work (GenBank Accession No: KC691302-KC691308) are labelled as F5 followed by in-house sequence IDs. (D) SNP profile of the 3’ recombination junction using the Sanger sequences, showing that nucleotide SNPs increased after the recombination junction.

    Article Snippet: Concentrations of the sRNA extracts were measured by using the Nanodrop 1000 UV-Vis spectrophotometer (Nanodrop Products, Wilmington, USA).

    Techniques: Sequencing, Reverse Transcription Polymerase Chain Reaction, Amplification, Construct

    Effect of aRNA purity and labelled-aRNA purification . (A) Graph showing coupling efficiency (C) and 320/650 (B) values for six MCF-7 aRNA samples with different 260/280 ratios. (B) Agilent Bioanalyzer pattern of MCF-7 Cy5-labelled target using an aRNA with 260/280 ratio of 1.6. Sharp spikes represent uncoupled Cy5 dye. (C) Same as B for aRNA with 260/280 ratio of 2 and coupling efficiency near 1. (D) NanoDrop ® ND-1000 Spectrophotometer absorptions at 320 and 650 nm wavelengths of a MCF-7 Cy5-labelled target. 320/650 ratio-0.6. (E) Same as in d (different sample). 320/650 ratio-0.09. (F) Recovery rates (R) and coupling efficiencies (C) for different labelled-aRNA purification methods. Data is presented for MCF-7 cell line and measurements represent an average of three separate reactions. Li-ETOH – LiCl-ethanol; PCI – phenol/chloroform/isoamyl alcohol.

    Journal: BMC Genomics

    Article Title: Expression microarray reproducibility is improved by optimising purification steps in RNA amplification and labelling

    doi: 10.1186/1471-2164-5-9

    Figure Lengend Snippet: Effect of aRNA purity and labelled-aRNA purification . (A) Graph showing coupling efficiency (C) and 320/650 (B) values for six MCF-7 aRNA samples with different 260/280 ratios. (B) Agilent Bioanalyzer pattern of MCF-7 Cy5-labelled target using an aRNA with 260/280 ratio of 1.6. Sharp spikes represent uncoupled Cy5 dye. (C) Same as B for aRNA with 260/280 ratio of 2 and coupling efficiency near 1. (D) NanoDrop ® ND-1000 Spectrophotometer absorptions at 320 and 650 nm wavelengths of a MCF-7 Cy5-labelled target. 320/650 ratio-0.6. (E) Same as in d (different sample). 320/650 ratio-0.09. (F) Recovery rates (R) and coupling efficiencies (C) for different labelled-aRNA purification methods. Data is presented for MCF-7 cell line and measurements represent an average of three separate reactions. Li-ETOH – LiCl-ethanol; PCI – phenol/chloroform/isoamyl alcohol.

    Article Snippet: Assessment of RNA quality The NanoDrop® ND-1000 Spectrophotometer (NanoDrop Technologies) was used to determine: 260/280 ratio, to assess total RNA and aRNA purity; 320/550 and 320/650 ratios, to evaluate Cy3 and Cy5-labelled aRNAs respectively.

    Techniques: Purification, Spectrophotometry

    Correspondence between the efficiency of humic acid removal and the pH of the extraction buffer, as assessed by eye (A) and NanoDrop ND-1000 spectrophotometry at 400 nm (B). Total RNA was extracted under either high-pH or low-pH conditions and was subsequently

    Journal: Applied and Environmental Microbiology

    Article Title: Extraction of mRNA from Soil ▿Extraction of mRNA from Soil ▿ †

    doi: 10.1128/AEM.03047-09

    Figure Lengend Snippet: Correspondence between the efficiency of humic acid removal and the pH of the extraction buffer, as assessed by eye (A) and NanoDrop ND-1000 spectrophotometry at 400 nm (B). Total RNA was extracted under either high-pH or low-pH conditions and was subsequently

    Article Snippet: Similarly, NanoDrop ND-1000 spectrophotometry (NanoDrop Technologies, United States) could not be used to quantify the RNA content, due to the overlapping absorption spectra of humic acids and RNA.

    Techniques: Spectrophotometry