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prunus necrotic ringspot virus pnrsv  (ATCC)


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    ATCC prunus necrotic ringspot virus pnrsv
    Primer set screening for RT-CPA assay of <t>PNRSV.</t> ( A ) Reaction curves of real-time RT-CPA. Fluorescence was monitored every 60 s, and one cycle shown here represents 1 min. ( B ) Target sequence and primer location of the primer set G7. Nucleotide positions are based on the PNRSV coat protein (CP)-encoding gene (Genbank No: NC-004364.1). The cross primer (5′-TGTTCCACCTTATAGTCCTGTACTGTTATAGTCCGAATGA-3′) covers the PNRSV-CPF (5′ to 3′) and PNRSV-MBR (3′ to 5′) sequences.
    Prunus Necrotic Ringspot Virus Pnrsv, supplied by ATCC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/prunus necrotic ringspot virus pnrsv/product/ATCC
    Average 90 stars, based on 1 article reviews
    prunus necrotic ringspot virus pnrsv - by Bioz Stars, 2026-02
    90/100 stars

    Images

    1) Product Images from "Rapid Detection of Prunus Necrotic Ringspot Virus by Reverse Transcription-cross-priming Amplification Coupled with Nucleic Acid Test Strip Cassette"

    Article Title: Rapid Detection of Prunus Necrotic Ringspot Virus by Reverse Transcription-cross-priming Amplification Coupled with Nucleic Acid Test Strip Cassette

    Journal: Scientific Reports

    doi: 10.1038/s41598-017-16536-6

    Primer set screening for RT-CPA assay of PNRSV. ( A ) Reaction curves of real-time RT-CPA. Fluorescence was monitored every 60 s, and one cycle shown here represents 1 min. ( B ) Target sequence and primer location of the primer set G7. Nucleotide positions are based on the PNRSV coat protein (CP)-encoding gene (Genbank No: NC-004364.1). The cross primer (5′-TGTTCCACCTTATAGTCCTGTACTGTTATAGTCCGAATGA-3′) covers the PNRSV-CPF (5′ to 3′) and PNRSV-MBR (3′ to 5′) sequences.
    Figure Legend Snippet: Primer set screening for RT-CPA assay of PNRSV. ( A ) Reaction curves of real-time RT-CPA. Fluorescence was monitored every 60 s, and one cycle shown here represents 1 min. ( B ) Target sequence and primer location of the primer set G7. Nucleotide positions are based on the PNRSV coat protein (CP)-encoding gene (Genbank No: NC-004364.1). The cross primer (5′-TGTTCCACCTTATAGTCCTGTACTGTTATAGTCCGAATGA-3′) covers the PNRSV-CPF (5′ to 3′) and PNRSV-MBR (3′ to 5′) sequences.

    Techniques Used: Fluorescence, Sequencing

    Specificity of RT-CPA-NATSC on the PNRSV detection. The reaction on PNRSV (lane 1) clearly showed both the test line and the control line, but only the control line were observed from the five common Prunus spp. pathogens, PPV, ASSVd, PLMVd, ApMV and ArMV (lane 2–6), as well as negative control and blank control (lane 7 and lane 8). Negative control, Totol RNA of healthy cucumber leaves; Blank control, RNase-free distilled water.
    Figure Legend Snippet: Specificity of RT-CPA-NATSC on the PNRSV detection. The reaction on PNRSV (lane 1) clearly showed both the test line and the control line, but only the control line were observed from the five common Prunus spp. pathogens, PPV, ASSVd, PLMVd, ApMV and ArMV (lane 2–6), as well as negative control and blank control (lane 7 and lane 8). Negative control, Totol RNA of healthy cucumber leaves; Blank control, RNase-free distilled water.

    Techniques Used: Control, Negative Control

    Sensitivity of RT-CPA-NATSC on PNRSV detection. ( A ) Comparison of the sensitivities of RT-CPA-NATSC (the upper pannel) and RT-PCR (the lower pannel) on the PNRSV detection. Lane1–5 represent 10 −1 –10 −5 dilution of total RNA of the PNRSV-infected cucumber sample, respectively. ( B ) The detection limit of RT-CPA-NATSC on PNRSV. Lane 1–6 represent 50 −1 –50 −5 dilution of pPNRSV-CP, respectively. Both the test line and the control line were indicated in lane 1-5.
    Figure Legend Snippet: Sensitivity of RT-CPA-NATSC on PNRSV detection. ( A ) Comparison of the sensitivities of RT-CPA-NATSC (the upper pannel) and RT-PCR (the lower pannel) on the PNRSV detection. Lane1–5 represent 10 −1 –10 −5 dilution of total RNA of the PNRSV-infected cucumber sample, respectively. ( B ) The detection limit of RT-CPA-NATSC on PNRSV. Lane 1–6 represent 50 −1 –50 −5 dilution of pPNRSV-CP, respectively. Both the test line and the control line were indicated in lane 1-5.

    Techniques Used: Comparison, Reverse Transcription Polymerase Chain Reaction, Infection, Control

    Detection of PNRSV in field samples with RT-CPA-NATSC (the upper pannel) and RT-PCR (the lower panel). Positive control, Total RNA of PNRSV infected cucumber leaves; Negative control, Total RNA of healthy cherry leaves; S1-S5, Total RNA of samples 1-5.
    Figure Legend Snippet: Detection of PNRSV in field samples with RT-CPA-NATSC (the upper pannel) and RT-PCR (the lower panel). Positive control, Total RNA of PNRSV infected cucumber leaves; Negative control, Total RNA of healthy cherry leaves; S1-S5, Total RNA of samples 1-5.

    Techniques Used: Reverse Transcription Polymerase Chain Reaction, Positive Control, Infection, Negative Control

    DAS-ELISA detection of PNRSV in field samples.
    Figure Legend Snippet: DAS-ELISA detection of PNRSV in field samples.

    Techniques Used: Positive Control, Negative Control

    Viruses and viroids used for the developmention of RT-CPA-NATSC assay.
    Figure Legend Snippet: Viruses and viroids used for the developmention of RT-CPA-NATSC assay.

    Techniques Used: Virus



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    prunus necrotic ringspot virus pnrsv  (ATCC)
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    ATCC prunus necrotic ringspot virus pnrsv
    Primer set screening for RT-CPA assay of <t>PNRSV.</t> ( A ) Reaction curves of real-time RT-CPA. Fluorescence was monitored every 60 s, and one cycle shown here represents 1 min. ( B ) Target sequence and primer location of the primer set G7. Nucleotide positions are based on the PNRSV coat protein (CP)-encoding gene (Genbank No: NC-004364.1). The cross primer (5′-TGTTCCACCTTATAGTCCTGTACTGTTATAGTCCGAATGA-3′) covers the PNRSV-CPF (5′ to 3′) and PNRSV-MBR (3′ to 5′) sequences.
    Prunus Necrotic Ringspot Virus Pnrsv, supplied by ATCC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/prunus necrotic ringspot virus pnrsv/product/ATCC
    Average 90 stars, based on 1 article reviews
    prunus necrotic ringspot virus pnrsv - by Bioz Stars, 2026-02
    90/100 stars
    		  Buy from Supplier

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    Primer set screening for RT-CPA assay of PNRSV. ( A ) Reaction curves of real-time RT-CPA. Fluorescence was monitored every 60 s, and one cycle shown here represents 1 min. ( B ) Target sequence and primer location of the primer set G7. Nucleotide positions are based on the PNRSV coat protein (CP)-encoding gene (Genbank No: NC-004364.1). The cross primer (5′-TGTTCCACCTTATAGTCCTGTACTGTTATAGTCCGAATGA-3′) covers the PNRSV-CPF (5′ to 3′) and PNRSV-MBR (3′ to 5′) sequences.

    Journal: Scientific Reports

    Article Title: Rapid Detection of Prunus Necrotic Ringspot Virus by Reverse Transcription-cross-priming Amplification Coupled with Nucleic Acid Test Strip Cassette

    doi: 10.1038/s41598-017-16536-6

    Figure Lengend Snippet: Primer set screening for RT-CPA assay of PNRSV. ( A ) Reaction curves of real-time RT-CPA. Fluorescence was monitored every 60 s, and one cycle shown here represents 1 min. ( B ) Target sequence and primer location of the primer set G7. Nucleotide positions are based on the PNRSV coat protein (CP)-encoding gene (Genbank No: NC-004364.1). The cross primer (5′-TGTTCCACCTTATAGTCCTGTACTGTTATAGTCCGAATGA-3′) covers the PNRSV-CPF (5′ to 3′) and PNRSV-MBR (3′ to 5′) sequences.

    Article Snippet: Prunus necrotic ringspot virus (PNRSV) , American Type Culture Collection (Manassas, VA, USA), ATCC (PV-552).

    Techniques: Fluorescence, Sequencing

    Specificity of RT-CPA-NATSC on the PNRSV detection. The reaction on PNRSV (lane 1) clearly showed both the test line and the control line, but only the control line were observed from the five common Prunus spp. pathogens, PPV, ASSVd, PLMVd, ApMV and ArMV (lane 2–6), as well as negative control and blank control (lane 7 and lane 8). Negative control, Totol RNA of healthy cucumber leaves; Blank control, RNase-free distilled water.

    Journal: Scientific Reports

    Article Title: Rapid Detection of Prunus Necrotic Ringspot Virus by Reverse Transcription-cross-priming Amplification Coupled with Nucleic Acid Test Strip Cassette

    doi: 10.1038/s41598-017-16536-6

    Figure Lengend Snippet: Specificity of RT-CPA-NATSC on the PNRSV detection. The reaction on PNRSV (lane 1) clearly showed both the test line and the control line, but only the control line were observed from the five common Prunus spp. pathogens, PPV, ASSVd, PLMVd, ApMV and ArMV (lane 2–6), as well as negative control and blank control (lane 7 and lane 8). Negative control, Totol RNA of healthy cucumber leaves; Blank control, RNase-free distilled water.

    Article Snippet: Prunus necrotic ringspot virus (PNRSV) , American Type Culture Collection (Manassas, VA, USA), ATCC (PV-552).

    Techniques: Control, Negative Control

    Sensitivity of RT-CPA-NATSC on PNRSV detection. ( A ) Comparison of the sensitivities of RT-CPA-NATSC (the upper pannel) and RT-PCR (the lower pannel) on the PNRSV detection. Lane1–5 represent 10 −1 –10 −5 dilution of total RNA of the PNRSV-infected cucumber sample, respectively. ( B ) The detection limit of RT-CPA-NATSC on PNRSV. Lane 1–6 represent 50 −1 –50 −5 dilution of pPNRSV-CP, respectively. Both the test line and the control line were indicated in lane 1-5.

    Journal: Scientific Reports

    Article Title: Rapid Detection of Prunus Necrotic Ringspot Virus by Reverse Transcription-cross-priming Amplification Coupled with Nucleic Acid Test Strip Cassette

    doi: 10.1038/s41598-017-16536-6

    Figure Lengend Snippet: Sensitivity of RT-CPA-NATSC on PNRSV detection. ( A ) Comparison of the sensitivities of RT-CPA-NATSC (the upper pannel) and RT-PCR (the lower pannel) on the PNRSV detection. Lane1–5 represent 10 −1 –10 −5 dilution of total RNA of the PNRSV-infected cucumber sample, respectively. ( B ) The detection limit of RT-CPA-NATSC on PNRSV. Lane 1–6 represent 50 −1 –50 −5 dilution of pPNRSV-CP, respectively. Both the test line and the control line were indicated in lane 1-5.

    Article Snippet: Prunus necrotic ringspot virus (PNRSV) , American Type Culture Collection (Manassas, VA, USA), ATCC (PV-552).

    Techniques: Comparison, Reverse Transcription Polymerase Chain Reaction, Infection, Control

    Detection of PNRSV in field samples with RT-CPA-NATSC (the upper pannel) and RT-PCR (the lower panel). Positive control, Total RNA of PNRSV infected cucumber leaves; Negative control, Total RNA of healthy cherry leaves; S1-S5, Total RNA of samples 1-5.

    Journal: Scientific Reports

    Article Title: Rapid Detection of Prunus Necrotic Ringspot Virus by Reverse Transcription-cross-priming Amplification Coupled with Nucleic Acid Test Strip Cassette

    doi: 10.1038/s41598-017-16536-6

    Figure Lengend Snippet: Detection of PNRSV in field samples with RT-CPA-NATSC (the upper pannel) and RT-PCR (the lower panel). Positive control, Total RNA of PNRSV infected cucumber leaves; Negative control, Total RNA of healthy cherry leaves; S1-S5, Total RNA of samples 1-5.

    Article Snippet: Prunus necrotic ringspot virus (PNRSV) , American Type Culture Collection (Manassas, VA, USA), ATCC (PV-552).

    Techniques: Reverse Transcription Polymerase Chain Reaction, Positive Control, Infection, Negative Control

    DAS-ELISA detection of PNRSV in field samples.

    Journal: Scientific Reports

    Article Title: Rapid Detection of Prunus Necrotic Ringspot Virus by Reverse Transcription-cross-priming Amplification Coupled with Nucleic Acid Test Strip Cassette

    doi: 10.1038/s41598-017-16536-6

    Figure Lengend Snippet: DAS-ELISA detection of PNRSV in field samples.

    Article Snippet: Prunus necrotic ringspot virus (PNRSV) , American Type Culture Collection (Manassas, VA, USA), ATCC (PV-552).

    Techniques: Positive Control, Negative Control

    Viruses and viroids used for the developmention of RT-CPA-NATSC assay.

    Journal: Scientific Reports

    Article Title: Rapid Detection of Prunus Necrotic Ringspot Virus by Reverse Transcription-cross-priming Amplification Coupled with Nucleic Acid Test Strip Cassette

    doi: 10.1038/s41598-017-16536-6

    Figure Lengend Snippet: Viruses and viroids used for the developmention of RT-CPA-NATSC assay.

    Article Snippet: Prunus necrotic ringspot virus (PNRSV) , American Type Culture Collection (Manassas, VA, USA), ATCC (PV-552).

    Techniques: Virus