confocal laser scanner scanarray lite (Lumonics Inc)
90
Structured Review
Lumonics Inc
confocal laser scanner scanarray lite
Confocal Laser Scanner Scanarray Lite, supplied by Lumonics Inc, 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/product/confocal+laser+scanner+scanarray+lite/confocal+laser+scanner+scanarray+lite/10__1007_slash_s12257___017___0215___z-51-10-16
Average 90 stars, based on 1 article reviews
Confocal Laser Scanner Scanarray Lite, supplied by Lumonics Inc, 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/product/confocal+laser+scanner+scanarray+lite/confocal+laser+scanner+scanarray+lite/10__1007_slash_s12257___017___0215___z-51-10-16
Average 90 stars, based on 1 article reviews
confocal laser scanner scanarray lite - by Bioz Stars,
2026-10
90/100 stars
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Microarray:Article Title: Specific multiplex analysis of pathogens using a direct 16S rRNA hybridization in microarray system. Article Snippet: For the rapid multiplex analysis of pathogens, 16S rRNAs from cell lysates were directly applied onto a DNA microarray at room temperature (RT) for RNA−DNA hybridization.. To eliminate the labeling step, seven fluorescent-labeled detector probes were cohybridized with 16S rRNA targets and adjacent specific capture probes.. We found that eight pathogens were successfully discriminated by the 16S rRNA-based direct method, which showed greater specificity than the polymerase chain reaction (PCR)-labeled method due to chaperone and distance effects. Article Title: Oligonucleotide microarrays with high discriminating power for the detection of single nucleotide variations in the p53 gene. Article Snippet: DNA microarrays are key tools for the parallel analysis of multiple DNA target samples and can be applicable to gene expression profiling and gene mutation analysis.. However, DNA microarrays have relatively poor accuracy for discrimination of perfectly-matched from single-base-mismatched duplexes; this demerit delays the diagnostic application of for genetic mutation analysis or detection of single nucleotide polymorphisms (SNPs) (Hacia, 1999; Lockhart et al., 1996; Rogler et al., 2004; Schena et al., 1995).. Poor accuracy of DNA microarrays for the detection of genetic mutation or SNPs is considered to originate partly from inherent characteristics of the solid surface for the microarray and its molecular interlayer structures. Article Title: Hybrid microarray based on double biomolecular markers of DNA and carbohydrate for simultaneous genotypic and phenotypic detection of cholera toxin-producing Vibrio cholerae. Article Snippet: Life-threatening diarrheal cholera is usually caused by water or food contaminated with cholera toxinproducing Vibrio cholerae.. For the prevention and surveillance of cholera, it is crucial to rapidly and precisely detect and identify the etiological causes, such as V. cholerae and/or its toxin.. In the present work, we propose the use of a hybrid double biomolecular marker (DBM) microarray containing 16S rRNA-based DNA capture probe to genotypically identify V. cholerae and GM1 pentasaccharide capture probe to phenotypically detect cholera toxin. Article Title: Specific Discrimination of Three Pathogenic Salmonella enterica subsp. enterica Serotypes by carB -Based Oligonucleotide Microarray Article Snippet: .. After the microarray was dried, the fluorescence intensity was scanned with a commercial Article Title: Multiplex 16S rRNA‐derived geno‐biochip for detection of 16 bacterial pathogens from contaminated foods Article Snippet: .. After drying, the geno‐biochip was scanned using a commercial Centrifugation:Article Title: Specific multiplex analysis of pathogens using a direct 16S rRNA hybridization in microarray system. Article Snippet: For the rapid multiplex analysis of pathogens, 16S rRNAs from cell lysates were directly applied onto a DNA microarray at room temperature (RT) for RNA−DNA hybridization.. To eliminate the labeling step, seven fluorescent-labeled detector probes were cohybridized with 16S rRNA targets and adjacent specific capture probes.. We found that eight pathogens were successfully discriminated by the 16S rRNA-based direct method, which showed greater specificity than the polymerase chain reaction (PCR)-labeled method due to chaperone and distance effects. Software:Article Title: Specific multiplex analysis of pathogens using a direct 16S rRNA hybridization in microarray system. Article Snippet: For the rapid multiplex analysis of pathogens, 16S rRNAs from cell lysates were directly applied onto a DNA microarray at room temperature (RT) for RNA−DNA hybridization.. To eliminate the labeling step, seven fluorescent-labeled detector probes were cohybridized with 16S rRNA targets and adjacent specific capture probes.. We found that eight pathogens were successfully discriminated by the 16S rRNA-based direct method, which showed greater specificity than the polymerase chain reaction (PCR)-labeled method due to chaperone and distance effects. Article Title: Optimization of DNA microarray biosensors enables rapid and sensitive detection Article Snippet: DNA microarray biosensors are essential tools for analyzing transcriptome expression levels and single nucleotide polymorphisms in disease pathology and diagnostics.. Since rapid and quantitative detection is necessary for these applications, optimization of the experimental conditions is essential.. Here, experimental conditions for DNA microarray biosensors were optimized using an artificial target strategy without reaction or purification bias. Article Title: Oligonucleotide microarrays with high discriminating power for the detection of single nucleotide variations in the p53 gene. Article Snippet: DNA microarrays are key tools for the parallel analysis of multiple DNA target samples and can be applicable to gene expression profiling and gene mutation analysis.. However, DNA microarrays have relatively poor accuracy for discrimination of perfectly-matched from single-base-mismatched duplexes; this demerit delays the diagnostic application of for genetic mutation analysis or detection of single nucleotide polymorphisms (SNPs) (Hacia, 1999; Lockhart et al., 1996; Rogler et al., 2004; Schena et al., 1995).. Poor accuracy of DNA microarrays for the detection of genetic mutation or SNPs is considered to originate partly from inherent characteristics of the solid surface for the microarray and its molecular interlayer structures. Article Title: Hybrid microarray based on double biomolecular markers of DNA and carbohydrate for simultaneous genotypic and phenotypic detection of cholera toxin-producing Vibrio cholerae. Article Snippet: Life-threatening diarrheal cholera is usually caused by water or food contaminated with cholera toxinproducing Vibrio cholerae.. For the prevention and surveillance of cholera, it is crucial to rapidly and precisely detect and identify the etiological causes, such as V. cholerae and/or its toxin.. In the present work, we propose the use of a hybrid double biomolecular marker (DBM) microarray containing 16S rRNA-based DNA capture probe to genotypically identify V. cholerae and GM1 pentasaccharide capture probe to phenotypically detect cholera toxin. Article Title: Specific Discrimination of Three Pathogenic Salmonella enterica subsp. enterica Serotypes by carB -Based Oligonucleotide Microarray Article Snippet: .. After the microarray was dried, the fluorescence intensity was scanned with a commercial Article Title: Multiplex 16S rRNA‐derived geno‐biochip for detection of 16 bacterial pathogens from contaminated foods Article Snippet: .. After drying, the geno‐biochip was scanned using a commercial Fluorescence:Article Title: Oligonucleotide microarrays with high discriminating power for the detection of single nucleotide variations in the p53 gene. Article Snippet: DNA microarrays are key tools for the parallel analysis of multiple DNA target samples and can be applicable to gene expression profiling and gene mutation analysis.. However, DNA microarrays have relatively poor accuracy for discrimination of perfectly-matched from single-base-mismatched duplexes; this demerit delays the diagnostic application of for genetic mutation analysis or detection of single nucleotide polymorphisms (SNPs) (Hacia, 1999; Lockhart et al., 1996; Rogler et al., 2004; Schena et al., 1995).. Poor accuracy of DNA microarrays for the detection of genetic mutation or SNPs is considered to originate partly from inherent characteristics of the solid surface for the microarray and its molecular interlayer structures. Article Title: Hybrid microarray based on double biomolecular markers of DNA and carbohydrate for simultaneous genotypic and phenotypic detection of cholera toxin-producing Vibrio cholerae. Article Snippet: Life-threatening diarrheal cholera is usually caused by water or food contaminated with cholera toxinproducing Vibrio cholerae.. For the prevention and surveillance of cholera, it is crucial to rapidly and precisely detect and identify the etiological causes, such as V. cholerae and/or its toxin.. In the present work, we propose the use of a hybrid double biomolecular marker (DBM) microarray containing 16S rRNA-based DNA capture probe to genotypically identify V. cholerae and GM1 pentasaccharide capture probe to phenotypically detect cholera toxin. Article Title: Specific Discrimination of Three Pathogenic Salmonella enterica subsp. enterica Serotypes by carB -Based Oligonucleotide Microarray Article Snippet: .. After the microarray was dried, the fluorescence intensity was scanned with a commercial |