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Eppendorf AG
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Qiagen
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Image Search Results
Journal: Virology Journal
Article Title: Comprehensive virome analysis of potato crops in Bangladesh reveals diverse viral communities and the first report of potato virus V
doi: 10.1186/s12985-026-03122-4
Figure Lengend Snippet: District-level prevalence of potato viruses in Bangladesh. Rows represent the surveyed regions (Rangpur, Dinajpur, Panchagarh, Thakurgaon, and Gazipur), while columns correspond to ten viruses detected by RT-PCR/PCR: PAMV (potato aucuba mosaic virus), PVX (potato virus X), PVM (potato virus M), PVS (potato virus S), PVV (potato virus V), PVA (potato virus A), PVY (potato virus Y), PLRV (potato leafroll virus), ToCV (tomato chlorosis virus), and ToLCNDV (tomato leaf curl New Delhi virus). Each cell indicates the percentage of infected samples (%) for a given virus in each district. The color scale (0–100%) reflects the relative prevalence. Overall, Dinajpur, Rangpur, and Panchagarh show higher viral burdens, whereas Gazipur and Thakurgaon exhibit relatively lower infection levels. Detailed data for each district are provided in Supplementary Table S3
Article Snippet: RT-PCR amplification was performed using the
Techniques: Reverse Transcription Polymerase Chain Reaction, Virus, Infection
Journal: Analytical Chemistry
Article Title: Development of a Lateral Flow Strip Membrane Assay for Rapid and Sensitive Detection of the SARS-CoV-2
doi: 10.1021/acs.analchem.0c03202
Figure Lengend Snippet: Figure 2. Selection of probes for the detection of SARS-CoV- 2. A) Chip map indicating positions of immobilized probes, Hybridization immobilized probes with the Cy-5 labeled RT- PCR products obtained by using B) no RNA templates (Nega- tive Control; NC), C) RNA template of RdRp gene, D) RNA template of ORF3a gene, E) RNA template of N gene, and F) Summarized fluorescence intensity day of each probe upon hybridization with the PCR products.
Article Snippet: The one-step RT-PCR premix (SuPrimeScript RT-PCR Premix 2X) and
Techniques: Selection, Hybridization, Labeling, Reverse Transcription Polymerase Chain Reaction, Control, Fluorescence