fish-quant 33 matlab tool Search Results


fish-quant 33 matlab tool  (MathWorks Inc)
90
MathWorks Inc fish-quant 33 matlab tool
a) Domain-level schematic of SDprobe_v1: Individual functional domains are annotated with their respective primary features in parentheses. Half-arrows indicate 3’-ends of the corresponding strands. The fluorophore and quencher are denoted by red and black circles respectively. b) Schematic of probe interaction with the 3’-UTR target sites (blue domains). Probes bind to the target sites via the short toehold domain, which initiates a 3-way branch migration step, ultimately displacing the quencher-labeled strand and thereby unquenching the fluorophore. Co-localization of multiple fluorophores on a single mRNA significantly increases the signal. c) Experimental workflow for detection of mRNAs using strand displacement probes: Probes are delivered via electroporation to cultured cells. Cells are incubated for 1 hour at 37°C allowing the probes to interact with mRNA target sites. Co-localization of up to 96 probes per mRNA generates a bright fluorescent spot detectable with fluorescence microscopy. After incubation, sequential image frames are collected at every 0.3 um z-distance across the cell height and the acquired frames are combined to generate maximum intensity projections representing the entire cell volume. These images are processed using the FISH-Quant33 <t>MATLAB</t> tool; a filtering step performs background signal correction and spots are pre-detected based on a threshold signal cut-off. The pre-detected spots are then fitted and examined for accuracy followed by spot quantification, where the spots are either selected or rejected based on signal intensity and elimination of false-positives. The selected spots represent the number of detected mRNAs per cell.
Fish Quant 33 Matlab Tool, supplied by MathWorks 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/result/fish-quant 33 matlab tool/product/MathWorks Inc
Average 90 stars, based on 1 article reviews
fish-quant 33 matlab tool - by Bioz Stars, 2026-03
90/100 stars
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fish-quant  (MathWorks Inc)
90
MathWorks Inc fish-quant
a) Domain-level schematic of SDprobe_v1: Individual functional domains are annotated with their respective primary features in parentheses. Half-arrows indicate 3’-ends of the corresponding strands. The fluorophore and quencher are denoted by red and black circles respectively. b) Schematic of probe interaction with the 3’-UTR target sites (blue domains). Probes bind to the target sites via the short toehold domain, which initiates a 3-way branch migration step, ultimately displacing the quencher-labeled strand and thereby unquenching the fluorophore. Co-localization of multiple fluorophores on a single mRNA significantly increases the signal. c) Experimental workflow for detection of mRNAs using strand displacement probes: Probes are delivered via electroporation to cultured cells. Cells are incubated for 1 hour at 37°C allowing the probes to interact with mRNA target sites. Co-localization of up to 96 probes per mRNA generates a bright fluorescent spot detectable with fluorescence microscopy. After incubation, sequential image frames are collected at every 0.3 um z-distance across the cell height and the acquired frames are combined to generate maximum intensity projections representing the entire cell volume. These images are processed using the FISH-Quant33 <t>MATLAB</t> tool; a filtering step performs background signal correction and spots are pre-detected based on a threshold signal cut-off. The pre-detected spots are then fitted and examined for accuracy followed by spot quantification, where the spots are either selected or rejected based on signal intensity and elimination of false-positives. The selected spots represent the number of detected mRNAs per cell.
Fish Quant, supplied by MathWorks 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/result/fish-quant/product/MathWorks Inc
Average 90 stars, based on 1 article reviews
fish-quant - by Bioz Stars, 2026-03
90/100 stars
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igor pro  (wavemetrics inc)
90
wavemetrics inc igor pro
a) Domain-level schematic of SDprobe_v1: Individual functional domains are annotated with their respective primary features in parentheses. Half-arrows indicate 3’-ends of the corresponding strands. The fluorophore and quencher are denoted by red and black circles respectively. b) Schematic of probe interaction with the 3’-UTR target sites (blue domains). Probes bind to the target sites via the short toehold domain, which initiates a 3-way branch migration step, ultimately displacing the quencher-labeled strand and thereby unquenching the fluorophore. Co-localization of multiple fluorophores on a single mRNA significantly increases the signal. c) Experimental workflow for detection of mRNAs using strand displacement probes: Probes are delivered via electroporation to cultured cells. Cells are incubated for 1 hour at 37°C allowing the probes to interact with mRNA target sites. Co-localization of up to 96 probes per mRNA generates a bright fluorescent spot detectable with fluorescence microscopy. After incubation, sequential image frames are collected at every 0.3 um z-distance across the cell height and the acquired frames are combined to generate maximum intensity projections representing the entire cell volume. These images are processed using the FISH-Quant33 <t>MATLAB</t> tool; a filtering step performs background signal correction and spots are pre-detected based on a threshold signal cut-off. The pre-detected spots are then fitted and examined for accuracy followed by spot quantification, where the spots are either selected or rejected based on signal intensity and elimination of false-positives. The selected spots represent the number of detected mRNAs per cell.
Igor Pro, supplied by wavemetrics 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/result/igor pro/product/wavemetrics inc
Average 90 stars, based on 1 article reviews
igor pro - by Bioz Stars, 2026-03
90/100 stars
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rlt buffer  (Qiagen)
90
Qiagen rlt buffer
a) Domain-level schematic of SDprobe_v1: Individual functional domains are annotated with their respective primary features in parentheses. Half-arrows indicate 3’-ends of the corresponding strands. The fluorophore and quencher are denoted by red and black circles respectively. b) Schematic of probe interaction with the 3’-UTR target sites (blue domains). Probes bind to the target sites via the short toehold domain, which initiates a 3-way branch migration step, ultimately displacing the quencher-labeled strand and thereby unquenching the fluorophore. Co-localization of multiple fluorophores on a single mRNA significantly increases the signal. c) Experimental workflow for detection of mRNAs using strand displacement probes: Probes are delivered via electroporation to cultured cells. Cells are incubated for 1 hour at 37°C allowing the probes to interact with mRNA target sites. Co-localization of up to 96 probes per mRNA generates a bright fluorescent spot detectable with fluorescence microscopy. After incubation, sequential image frames are collected at every 0.3 um z-distance across the cell height and the acquired frames are combined to generate maximum intensity projections representing the entire cell volume. These images are processed using the FISH-Quant33 <t>MATLAB</t> tool; a filtering step performs background signal correction and spots are pre-detected based on a threshold signal cut-off. The pre-detected spots are then fitted and examined for accuracy followed by spot quantification, where the spots are either selected or rejected based on signal intensity and elimination of false-positives. The selected spots represent the number of detected mRNAs per cell.
Rlt Buffer, supplied by Qiagen, 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/rlt buffer/product/Qiagen
Average 90 stars, based on 1 article reviews
rlt buffer - by Bioz Stars, 2026-03
90/100 stars
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stellaris oligonucleotides sets  (Biosearch Technologies Inc)
90
Biosearch Technologies Inc stellaris oligonucleotides sets
a) Domain-level schematic of SDprobe_v1: Individual functional domains are annotated with their respective primary features in parentheses. Half-arrows indicate 3’-ends of the corresponding strands. The fluorophore and quencher are denoted by red and black circles respectively. b) Schematic of probe interaction with the 3’-UTR target sites (blue domains). Probes bind to the target sites via the short toehold domain, which initiates a 3-way branch migration step, ultimately displacing the quencher-labeled strand and thereby unquenching the fluorophore. Co-localization of multiple fluorophores on a single mRNA significantly increases the signal. c) Experimental workflow for detection of mRNAs using strand displacement probes: Probes are delivered via electroporation to cultured cells. Cells are incubated for 1 hour at 37°C allowing the probes to interact with mRNA target sites. Co-localization of up to 96 probes per mRNA generates a bright fluorescent spot detectable with fluorescence microscopy. After incubation, sequential image frames are collected at every 0.3 um z-distance across the cell height and the acquired frames are combined to generate maximum intensity projections representing the entire cell volume. These images are processed using the FISH-Quant33 <t>MATLAB</t> tool; a filtering step performs background signal correction and spots are pre-detected based on a threshold signal cut-off. The pre-detected spots are then fitted and examined for accuracy followed by spot quantification, where the spots are either selected or rejected based on signal intensity and elimination of false-positives. The selected spots represent the number of detected mRNAs per cell.
Stellaris Oligonucleotides Sets, supplied by Biosearch Technologies 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/result/stellaris oligonucleotides sets/product/Biosearch Technologies Inc
Average 90 stars, based on 1 article reviews
stellaris oligonucleotides sets - by Bioz Stars, 2026-03
90/100 stars
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Image Search Results


a) Domain-level schematic of SDprobe_v1: Individual functional domains are annotated with their respective primary features in parentheses. Half-arrows indicate 3’-ends of the corresponding strands. The fluorophore and quencher are denoted by red and black circles respectively. b) Schematic of probe interaction with the 3’-UTR target sites (blue domains). Probes bind to the target sites via the short toehold domain, which initiates a 3-way branch migration step, ultimately displacing the quencher-labeled strand and thereby unquenching the fluorophore. Co-localization of multiple fluorophores on a single mRNA significantly increases the signal. c) Experimental workflow for detection of mRNAs using strand displacement probes: Probes are delivered via electroporation to cultured cells. Cells are incubated for 1 hour at 37°C allowing the probes to interact with mRNA target sites. Co-localization of up to 96 probes per mRNA generates a bright fluorescent spot detectable with fluorescence microscopy. After incubation, sequential image frames are collected at every 0.3 um z-distance across the cell height and the acquired frames are combined to generate maximum intensity projections representing the entire cell volume. These images are processed using the FISH-Quant33 MATLAB tool; a filtering step performs background signal correction and spots are pre-detected based on a threshold signal cut-off. The pre-detected spots are then fitted and examined for accuracy followed by spot quantification, where the spots are either selected or rejected based on signal intensity and elimination of false-positives. The selected spots represent the number of detected mRNAs per cell.

Journal: ACS synthetic biology

Article Title: Nucleic Acid Strand Displacement with Synthetic mRNA Inputs in Living Mammalian Cells

doi: 10.1021/acssynbio.8b00288

Figure Lengend Snippet: a) Domain-level schematic of SDprobe_v1: Individual functional domains are annotated with their respective primary features in parentheses. Half-arrows indicate 3’-ends of the corresponding strands. The fluorophore and quencher are denoted by red and black circles respectively. b) Schematic of probe interaction with the 3’-UTR target sites (blue domains). Probes bind to the target sites via the short toehold domain, which initiates a 3-way branch migration step, ultimately displacing the quencher-labeled strand and thereby unquenching the fluorophore. Co-localization of multiple fluorophores on a single mRNA significantly increases the signal. c) Experimental workflow for detection of mRNAs using strand displacement probes: Probes are delivered via electroporation to cultured cells. Cells are incubated for 1 hour at 37°C allowing the probes to interact with mRNA target sites. Co-localization of up to 96 probes per mRNA generates a bright fluorescent spot detectable with fluorescence microscopy. After incubation, sequential image frames are collected at every 0.3 um z-distance across the cell height and the acquired frames are combined to generate maximum intensity projections representing the entire cell volume. These images are processed using the FISH-Quant33 MATLAB tool; a filtering step performs background signal correction and spots are pre-detected based on a threshold signal cut-off. The pre-detected spots are then fitted and examined for accuracy followed by spot quantification, where the spots are either selected or rejected based on signal intensity and elimination of false-positives. The selected spots represent the number of detected mRNAs per cell.

Article Snippet: These images are processed using the FISH-Quant 33 MATLAB tool; a filtering step performs background signal correction and spots are pre-detected based on a threshold signal cut-off.

Techniques: Functional Assay, Migration, Labeling, Electroporation, Cell Culture, Incubation, Fluorescence, Microscopy