mon810 genomic dna gdna  (New England Biolabs)


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    New England Biolabs mon810 genomic dna gdna
    <t>MON810</t> content measured by ddPCR in five series of seven replicates. The aggregate represents the sum of the five series. The target certified MON810 content (0.77%) is indicated by a dotted line. Acceptance criterion for repeatability is ±25% of the target content (from 0.58% to 0.96%) represented by the dashed lines. Error bars represent the standard deviation between the replicates for each series or in the aggregate.
    Mon810 Genomic Dna Gdna, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    mon810 genomic dna gdna - by Bioz Stars, 2023-01
    99/100 stars

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    1) Product Images from "Quantitative Analysis of Food and Feed Samples with Droplet Digital PCR"

    Article Title: Quantitative Analysis of Food and Feed Samples with Droplet Digital PCR

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0062583

    MON810 content measured by ddPCR in five series of seven replicates. The aggregate represents the sum of the five series. The target certified MON810 content (0.77%) is indicated by a dotted line. Acceptance criterion for repeatability is ±25% of the target content (from 0.58% to 0.96%) represented by the dashed lines. Error bars represent the standard deviation between the replicates for each series or in the aggregate.
    Figure Legend Snippet: MON810 content measured by ddPCR in five series of seven replicates. The aggregate represents the sum of the five series. The target certified MON810 content (0.77%) is indicated by a dotted line. Acceptance criterion for repeatability is ±25% of the target content (from 0.58% to 0.96%) represented by the dashed lines. Error bars represent the standard deviation between the replicates for each series or in the aggregate.

    Techniques Used: Standard Deviation

    MON810 content measured by ddPCR in five series of seven target concentrations. The target MON810 content (3.85%) is indicated by a dotted line. Acceptance criterion for precision is ±25% of the target content (from 2.89% to 4.81%) represented by the dashed lines. Error bars represent the standard deviation of the measured MON810% by ddPCR at each target concentration (five replicates per target concentration).
    Figure Legend Snippet: MON810 content measured by ddPCR in five series of seven target concentrations. The target MON810 content (3.85%) is indicated by a dotted line. Acceptance criterion for precision is ±25% of the target content (from 2.89% to 4.81%) represented by the dashed lines. Error bars represent the standard deviation of the measured MON810% by ddPCR at each target concentration (five replicates per target concentration).

    Techniques Used: Standard Deviation, Concentration Assay

    Summary table of qPCR, ddPCR and cdPCR performance for  MON810  detection and quantification.
    Figure Legend Snippet: Summary table of qPCR, ddPCR and cdPCR performance for MON810 detection and quantification.

    Techniques Used: Plasmid Preparation, Inhibition, DNA Extraction

    mon810 genomic dna gdna  (New England Biolabs)


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    New England Biolabs mon810 genomic dna gdna
    <t>MON810</t> content measured by ddPCR in five series of seven replicates. The aggregate represents the sum of the five series. The target certified MON810 content (0.77%) is indicated by a dotted line. Acceptance criterion for repeatability is ±25% of the target content (from 0.58% to 0.96%) represented by the dashed lines. Error bars represent the standard deviation between the replicates for each series or in the aggregate.
    Mon810 Genomic Dna Gdna, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mon810 genomic dna gdna/product/New England Biolabs
    Average 99 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    mon810 genomic dna gdna - by Bioz Stars, 2023-01
    99/100 stars

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    1) Product Images from "Quantitative Analysis of Food and Feed Samples with Droplet Digital PCR"

    Article Title: Quantitative Analysis of Food and Feed Samples with Droplet Digital PCR

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0062583

    MON810 content measured by ddPCR in five series of seven replicates. The aggregate represents the sum of the five series. The target certified MON810 content (0.77%) is indicated by a dotted line. Acceptance criterion for repeatability is ±25% of the target content (from 0.58% to 0.96%) represented by the dashed lines. Error bars represent the standard deviation between the replicates for each series or in the aggregate.
    Figure Legend Snippet: MON810 content measured by ddPCR in five series of seven replicates. The aggregate represents the sum of the five series. The target certified MON810 content (0.77%) is indicated by a dotted line. Acceptance criterion for repeatability is ±25% of the target content (from 0.58% to 0.96%) represented by the dashed lines. Error bars represent the standard deviation between the replicates for each series or in the aggregate.

    Techniques Used: Standard Deviation

    MON810 content measured by ddPCR in five series of seven target concentrations. The target MON810 content (3.85%) is indicated by a dotted line. Acceptance criterion for precision is ±25% of the target content (from 2.89% to 4.81%) represented by the dashed lines. Error bars represent the standard deviation of the measured MON810% by ddPCR at each target concentration (five replicates per target concentration).
    Figure Legend Snippet: MON810 content measured by ddPCR in five series of seven target concentrations. The target MON810 content (3.85%) is indicated by a dotted line. Acceptance criterion for precision is ±25% of the target content (from 2.89% to 4.81%) represented by the dashed lines. Error bars represent the standard deviation of the measured MON810% by ddPCR at each target concentration (five replicates per target concentration).

    Techniques Used: Standard Deviation, Concentration Assay

    Summary table of qPCR, ddPCR and cdPCR performance for  MON810  detection and quantification.
    Figure Legend Snippet: Summary table of qPCR, ddPCR and cdPCR performance for MON810 detection and quantification.

    Techniques Used: Plasmid Preparation, Inhibition, DNA Extraction

    qualified fragmented gdna  (New England Biolabs)


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    New England Biolabs qualified fragmented gdna
    Qualified Fragmented Gdna, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    gdna cleaning column steps  (New England Biolabs)


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    New England Biolabs gdna cleaning column steps
    Gdna Cleaning Column Steps, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    genomic dna gdna  (New England Biolabs)


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    New England Biolabs genomic dna gdna
    Genomic Dna Gdna, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    monarch gdna purification kit  (New England Biolabs)


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    New England Biolabs monarch gdna purification kit
    Monarch Gdna Purification Kit, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    residual gdna  (New England Biolabs)


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    New England Biolabs residual gdna
    DEK504 is required for nad3 -44 and nad3 -317 C-to-U editing in maize mitochondria. ( a ) Analysis <t>of</t> <t>RNA</t> editing in nad3 transcripts of wildtype (WT) and dek504-ref kernels. The editing sites are indicated by the red lines. Codons harboring the edited nucleotides and coded amino acids are shown. ( b ) Alignment of amino acid residues at positions 6 and 1′ in each PPR motif of DEK504 with a −1 to −15 bp upstream sequence of these four defective editing sites. Nucleotides matching the recognition code of DEK504 in nad3 are shown in blue. The edited C residues in nad3 are shown in red. ( c ) Alignment of the neighboring <t>gDNA</t> sequences of nad3. The gDNA and cDNA sequences were obtained from the NCBI database. Monocots included Zea luxurians , Hordeum vulgare , Sorghum bicolor , Triticum aestivum , Bambusa oldhamii , Avena sativa , Phoenix dactylifera , Stipa capillata , Allium cepa , and Coix lacryma-jobi . Dicots-I included Arabidopsis thaliana , Brassica juncea , Brassica rapa , Brassica napus , and Boechera stricta . Dicots-II included Gossypium trilobum , Lagerstroemia indica , Bombax ceiba , Fagus sylvatica , Manihot esculenta , Heuchera parviflora , Malania oleifera , and Damnacanthus indicus . Dicots-III included Cannabis sativa , Panax vietnamensis , Panax notoginseng , and Tamarindus indica. Red triangles indicate the positions affected by nad3 -44 and nad3 -317.
    Residual Gdna, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Dek504 Encodes a Mitochondrion-Targeted E+-Type Pentatricopeptide Repeat Protein Essential for RNA Editing and Seed Development in Maize"

    Article Title: Dek504 Encodes a Mitochondrion-Targeted E+-Type Pentatricopeptide Repeat Protein Essential for RNA Editing and Seed Development in Maize

    Journal: International Journal of Molecular Sciences

    doi: 10.3390/ijms23052513

    DEK504 is required for nad3 -44 and nad3 -317 C-to-U editing in maize mitochondria. ( a ) Analysis of RNA editing in nad3 transcripts of wildtype (WT) and dek504-ref kernels. The editing sites are indicated by the red lines. Codons harboring the edited nucleotides and coded amino acids are shown. ( b ) Alignment of amino acid residues at positions 6 and 1′ in each PPR motif of DEK504 with a −1 to −15 bp upstream sequence of these four defective editing sites. Nucleotides matching the recognition code of DEK504 in nad3 are shown in blue. The edited C residues in nad3 are shown in red. ( c ) Alignment of the neighboring gDNA sequences of nad3. The gDNA and cDNA sequences were obtained from the NCBI database. Monocots included Zea luxurians , Hordeum vulgare , Sorghum bicolor , Triticum aestivum , Bambusa oldhamii , Avena sativa , Phoenix dactylifera , Stipa capillata , Allium cepa , and Coix lacryma-jobi . Dicots-I included Arabidopsis thaliana , Brassica juncea , Brassica rapa , Brassica napus , and Boechera stricta . Dicots-II included Gossypium trilobum , Lagerstroemia indica , Bombax ceiba , Fagus sylvatica , Manihot esculenta , Heuchera parviflora , Malania oleifera , and Damnacanthus indicus . Dicots-III included Cannabis sativa , Panax vietnamensis , Panax notoginseng , and Tamarindus indica. Red triangles indicate the positions affected by nad3 -44 and nad3 -317.
    Figure Legend Snippet: DEK504 is required for nad3 -44 and nad3 -317 C-to-U editing in maize mitochondria. ( a ) Analysis of RNA editing in nad3 transcripts of wildtype (WT) and dek504-ref kernels. The editing sites are indicated by the red lines. Codons harboring the edited nucleotides and coded amino acids are shown. ( b ) Alignment of amino acid residues at positions 6 and 1′ in each PPR motif of DEK504 with a −1 to −15 bp upstream sequence of these four defective editing sites. Nucleotides matching the recognition code of DEK504 in nad3 are shown in blue. The edited C residues in nad3 are shown in red. ( c ) Alignment of the neighboring gDNA sequences of nad3. The gDNA and cDNA sequences were obtained from the NCBI database. Monocots included Zea luxurians , Hordeum vulgare , Sorghum bicolor , Triticum aestivum , Bambusa oldhamii , Avena sativa , Phoenix dactylifera , Stipa capillata , Allium cepa , and Coix lacryma-jobi . Dicots-I included Arabidopsis thaliana , Brassica juncea , Brassica rapa , Brassica napus , and Boechera stricta . Dicots-II included Gossypium trilobum , Lagerstroemia indica , Bombax ceiba , Fagus sylvatica , Manihot esculenta , Heuchera parviflora , Malania oleifera , and Damnacanthus indicus . Dicots-III included Cannabis sativa , Panax vietnamensis , Panax notoginseng , and Tamarindus indica. Red triangles indicate the positions affected by nad3 -44 and nad3 -317.

    Techniques Used: Sequencing

    genomic dna gdna  (New England Biolabs)


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    New England Biolabs genomic dna gdna
    Genomic Dna Gdna, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    gdna cleaning column steps  (New England Biolabs)


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    monarch gdna purification kit  (New England Biolabs)


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    New England Biolabs monarch gdna purification kit
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    genomic dna gdna  (New England Biolabs)


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    New England Biolabs genomic dna gdna
    Genomic Dna Gdna, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    New England Biolabs mon810 genomic dna gdna
    <t>MON810</t> content measured by ddPCR in five series of seven replicates. The aggregate represents the sum of the five series. The target certified MON810 content (0.77%) is indicated by a dotted line. Acceptance criterion for repeatability is ±25% of the target content (from 0.58% to 0.96%) represented by the dashed lines. Error bars represent the standard deviation between the replicates for each series or in the aggregate.
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    https://www.bioz.com/result/mon810 genomic dna gdna/product/New England Biolabs
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    New England Biolabs qualified fragmented gdna
    <t>MON810</t> content measured by ddPCR in five series of seven replicates. The aggregate represents the sum of the five series. The target certified MON810 content (0.77%) is indicated by a dotted line. Acceptance criterion for repeatability is ±25% of the target content (from 0.58% to 0.96%) represented by the dashed lines. Error bars represent the standard deviation between the replicates for each series or in the aggregate.
    Qualified Fragmented Gdna, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    New England Biolabs gdna cleaning column steps
    <t>MON810</t> content measured by ddPCR in five series of seven replicates. The aggregate represents the sum of the five series. The target certified MON810 content (0.77%) is indicated by a dotted line. Acceptance criterion for repeatability is ±25% of the target content (from 0.58% to 0.96%) represented by the dashed lines. Error bars represent the standard deviation between the replicates for each series or in the aggregate.
    Gdna Cleaning Column Steps, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    New England Biolabs genomic dna gdna
    <t>MON810</t> content measured by ddPCR in five series of seven replicates. The aggregate represents the sum of the five series. The target certified MON810 content (0.77%) is indicated by a dotted line. Acceptance criterion for repeatability is ±25% of the target content (from 0.58% to 0.96%) represented by the dashed lines. Error bars represent the standard deviation between the replicates for each series or in the aggregate.
    Genomic Dna Gdna, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    New England Biolabs monarch gdna purification kit
    <t>MON810</t> content measured by ddPCR in five series of seven replicates. The aggregate represents the sum of the five series. The target certified MON810 content (0.77%) is indicated by a dotted line. Acceptance criterion for repeatability is ±25% of the target content (from 0.58% to 0.96%) represented by the dashed lines. Error bars represent the standard deviation between the replicates for each series or in the aggregate.
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    New England Biolabs residual gdna
    DEK504 is required for nad3 -44 and nad3 -317 C-to-U editing in maize mitochondria. ( a ) Analysis <t>of</t> <t>RNA</t> editing in nad3 transcripts of wildtype (WT) and dek504-ref kernels. The editing sites are indicated by the red lines. Codons harboring the edited nucleotides and coded amino acids are shown. ( b ) Alignment of amino acid residues at positions 6 and 1′ in each PPR motif of DEK504 with a −1 to −15 bp upstream sequence of these four defective editing sites. Nucleotides matching the recognition code of DEK504 in nad3 are shown in blue. The edited C residues in nad3 are shown in red. ( c ) Alignment of the neighboring <t>gDNA</t> sequences of nad3. The gDNA and cDNA sequences were obtained from the NCBI database. Monocots included Zea luxurians , Hordeum vulgare , Sorghum bicolor , Triticum aestivum , Bambusa oldhamii , Avena sativa , Phoenix dactylifera , Stipa capillata , Allium cepa , and Coix lacryma-jobi . Dicots-I included Arabidopsis thaliana , Brassica juncea , Brassica rapa , Brassica napus , and Boechera stricta . Dicots-II included Gossypium trilobum , Lagerstroemia indica , Bombax ceiba , Fagus sylvatica , Manihot esculenta , Heuchera parviflora , Malania oleifera , and Damnacanthus indicus . Dicots-III included Cannabis sativa , Panax vietnamensis , Panax notoginseng , and Tamarindus indica. Red triangles indicate the positions affected by nad3 -44 and nad3 -317.
    Residual Gdna, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    MON810 content measured by ddPCR in five series of seven replicates. The aggregate represents the sum of the five series. The target certified MON810 content (0.77%) is indicated by a dotted line. Acceptance criterion for repeatability is ±25% of the target content (from 0.58% to 0.96%) represented by the dashed lines. Error bars represent the standard deviation between the replicates for each series or in the aggregate.

    Journal: PLoS ONE

    Article Title: Quantitative Analysis of Food and Feed Samples with Droplet Digital PCR

    doi: 10.1371/journal.pone.0062583

    Figure Lengend Snippet: MON810 content measured by ddPCR in five series of seven replicates. The aggregate represents the sum of the five series. The target certified MON810 content (0.77%) is indicated by a dotted line. Acceptance criterion for repeatability is ±25% of the target content (from 0.58% to 0.96%) represented by the dashed lines. Error bars represent the standard deviation between the replicates for each series or in the aggregate.

    Article Snippet: Enzymatic digestion of MON810 genomic DNA (gDNA) with Taq I (New England Biolabs GmbH, Frankfurt am Main, Germany) was performed as described (see ) .

    Techniques: Standard Deviation

    MON810 content measured by ddPCR in five series of seven target concentrations. The target MON810 content (3.85%) is indicated by a dotted line. Acceptance criterion for precision is ±25% of the target content (from 2.89% to 4.81%) represented by the dashed lines. Error bars represent the standard deviation of the measured MON810% by ddPCR at each target concentration (five replicates per target concentration).

    Journal: PLoS ONE

    Article Title: Quantitative Analysis of Food and Feed Samples with Droplet Digital PCR

    doi: 10.1371/journal.pone.0062583

    Figure Lengend Snippet: MON810 content measured by ddPCR in five series of seven target concentrations. The target MON810 content (3.85%) is indicated by a dotted line. Acceptance criterion for precision is ±25% of the target content (from 2.89% to 4.81%) represented by the dashed lines. Error bars represent the standard deviation of the measured MON810% by ddPCR at each target concentration (five replicates per target concentration).

    Article Snippet: Enzymatic digestion of MON810 genomic DNA (gDNA) with Taq I (New England Biolabs GmbH, Frankfurt am Main, Germany) was performed as described (see ) .

    Techniques: Standard Deviation, Concentration Assay

    Summary table of qPCR, ddPCR and cdPCR performance for  MON810  detection and quantification.

    Journal: PLoS ONE

    Article Title: Quantitative Analysis of Food and Feed Samples with Droplet Digital PCR

    doi: 10.1371/journal.pone.0062583

    Figure Lengend Snippet: Summary table of qPCR, ddPCR and cdPCR performance for MON810 detection and quantification.

    Article Snippet: Enzymatic digestion of MON810 genomic DNA (gDNA) with Taq I (New England Biolabs GmbH, Frankfurt am Main, Germany) was performed as described (see ) .

    Techniques: Plasmid Preparation, Inhibition, DNA Extraction

    DEK504 is required for nad3 -44 and nad3 -317 C-to-U editing in maize mitochondria. ( a ) Analysis of RNA editing in nad3 transcripts of wildtype (WT) and dek504-ref kernels. The editing sites are indicated by the red lines. Codons harboring the edited nucleotides and coded amino acids are shown. ( b ) Alignment of amino acid residues at positions 6 and 1′ in each PPR motif of DEK504 with a −1 to −15 bp upstream sequence of these four defective editing sites. Nucleotides matching the recognition code of DEK504 in nad3 are shown in blue. The edited C residues in nad3 are shown in red. ( c ) Alignment of the neighboring gDNA sequences of nad3. The gDNA and cDNA sequences were obtained from the NCBI database. Monocots included Zea luxurians , Hordeum vulgare , Sorghum bicolor , Triticum aestivum , Bambusa oldhamii , Avena sativa , Phoenix dactylifera , Stipa capillata , Allium cepa , and Coix lacryma-jobi . Dicots-I included Arabidopsis thaliana , Brassica juncea , Brassica rapa , Brassica napus , and Boechera stricta . Dicots-II included Gossypium trilobum , Lagerstroemia indica , Bombax ceiba , Fagus sylvatica , Manihot esculenta , Heuchera parviflora , Malania oleifera , and Damnacanthus indicus . Dicots-III included Cannabis sativa , Panax vietnamensis , Panax notoginseng , and Tamarindus indica. Red triangles indicate the positions affected by nad3 -44 and nad3 -317.

    Journal: International Journal of Molecular Sciences

    Article Title: Dek504 Encodes a Mitochondrion-Targeted E+-Type Pentatricopeptide Repeat Protein Essential for RNA Editing and Seed Development in Maize

    doi: 10.3390/ijms23052513

    Figure Lengend Snippet: DEK504 is required for nad3 -44 and nad3 -317 C-to-U editing in maize mitochondria. ( a ) Analysis of RNA editing in nad3 transcripts of wildtype (WT) and dek504-ref kernels. The editing sites are indicated by the red lines. Codons harboring the edited nucleotides and coded amino acids are shown. ( b ) Alignment of amino acid residues at positions 6 and 1′ in each PPR motif of DEK504 with a −1 to −15 bp upstream sequence of these four defective editing sites. Nucleotides matching the recognition code of DEK504 in nad3 are shown in blue. The edited C residues in nad3 are shown in red. ( c ) Alignment of the neighboring gDNA sequences of nad3. The gDNA and cDNA sequences were obtained from the NCBI database. Monocots included Zea luxurians , Hordeum vulgare , Sorghum bicolor , Triticum aestivum , Bambusa oldhamii , Avena sativa , Phoenix dactylifera , Stipa capillata , Allium cepa , and Coix lacryma-jobi . Dicots-I included Arabidopsis thaliana , Brassica juncea , Brassica rapa , Brassica napus , and Boechera stricta . Dicots-II included Gossypium trilobum , Lagerstroemia indica , Bombax ceiba , Fagus sylvatica , Manihot esculenta , Heuchera parviflora , Malania oleifera , and Damnacanthus indicus . Dicots-III included Cannabis sativa , Panax vietnamensis , Panax notoginseng , and Tamarindus indica. Red triangles indicate the positions affected by nad3 -44 and nad3 -317.

    Article Snippet: RNA was extracted using a commercial kit (Tiangen, Beijing, China), and residual gDNA was removed with RNAse-free DNAse I (NEB) treatment.

    Techniques: Sequencing