fluorescent band intensity Search Results


fluorescent band intensity  (Cytiva Europe)
95
Cytiva Europe fluorescent band intensity
Fluorescent Band Intensity, supplied by Cytiva Europe, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fluorescent+band+intensity/ImageQuant+TL+8%2E1%2C+node+locked+license/pmc09309538-111-0-20
Average 95 stars, based on 1 article reviews
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li cor odyssey imaging system  (LI-COR)
99
LI-COR li cor odyssey imaging system
Li Cor Odyssey Imaging System, supplied by LI-COR, 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/product/fluorescent+band+intensity/Odyssey+Imaging+System/pm30829469-162-10-10
Average 99 stars, based on 1 article reviews
li cor odyssey imaging system - by Bioz Stars, 2026-10
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dna band fluorescent intensities  (Thermo Fisher)
99
Thermo Fisher dna band fluorescent intensities
PCR amplification of <t>DNA</t> containing each of nine different microsatellites from each progeny plant with one of each locus-specific primer pairs, analysis of product mixtures <t>by</t> <t>capillary</t> electrophoresis, detection of fluorescent products, and generation of electropherograms were as described under “Materials and Methods.” A, Electropherograms showing all PCR products; one of each primer pair was labeled with FAM or HEX fluorescent dye. B, Representative electropherogram patterns for locus NGA1107. Apparent absolute size of primary wild-type (wt) product band is 317 bp. Shown also are products where both alleles showed an increase of one repeat unit, increasing apparent product length to 319 bp (+2), where one allele maintained wild-type length and one showed a loss of one repeat [wt & (-2)], and where one allele remained wild type and one showed a shift of two repeats, decreasing apparent length to 313 bp [wt & (-4)]. Arrows indicate position of 317-bp (wild-type) product. C, Patterns for reconstruction mixtures. DNA from plants homozygous (pure) for alleles at locus NGA1107 encoding 313-bp (black arrow) or 315-bp (gray arrow) products or mixtures of the two at indicated ratios (concentrations of DNAs measured before PCR by staining with PicoGreen [Molecular Probes, Eugene, OR]) were analyzed as described above. Note that the primary criterion for scoring a pattern as reflecting a mixture of two different length products—second peak from right greater than a significantly large first peak—is met only for 1:1 and 2:1 mixtures.
Dna Band Fluorescent Intensities, supplied by Thermo Fisher, 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/product/fluorescent+band+intensity/DNA/pmc00196609-366-25-30
Average 99 stars, based on 1 article reviews
dna band fluorescent intensities - by Bioz Stars, 2026-10
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cyan fluorescent protein intensity  (IDEX)
90
IDEX cyan fluorescent protein intensity
PCR amplification of <t>DNA</t> containing each of nine different microsatellites from each progeny plant with one of each locus-specific primer pairs, analysis of product mixtures <t>by</t> <t>capillary</t> electrophoresis, detection of fluorescent products, and generation of electropherograms were as described under “Materials and Methods.” A, Electropherograms showing all PCR products; one of each primer pair was labeled with FAM or HEX fluorescent dye. B, Representative electropherogram patterns for locus NGA1107. Apparent absolute size of primary wild-type (wt) product band is 317 bp. Shown also are products where both alleles showed an increase of one repeat unit, increasing apparent product length to 319 bp (+2), where one allele maintained wild-type length and one showed a loss of one repeat [wt & (-2)], and where one allele remained wild type and one showed a shift of two repeats, decreasing apparent length to 313 bp [wt & (-4)]. Arrows indicate position of 317-bp (wild-type) product. C, Patterns for reconstruction mixtures. DNA from plants homozygous (pure) for alleles at locus NGA1107 encoding 313-bp (black arrow) or 315-bp (gray arrow) products or mixtures of the two at indicated ratios (concentrations of DNAs measured before PCR by staining with PicoGreen [Molecular Probes, Eugene, OR]) were analyzed as described above. Note that the primary criterion for scoring a pattern as reflecting a mixture of two different length products—second peak from right greater than a significantly large first peak—is met only for 1:1 and 2:1 mixtures.
Cyan Fluorescent Protein Intensity, supplied by IDEX, 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/fluorescent+band+intensity/enhanced+cyan+fluorescent+protein++ecfp+/pmc03069478-82-11-20
Average 90 stars, based on 1 article reviews
cyan fluorescent protein intensity - by Bioz Stars, 2026-10
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fluorescence scanner  (LI-COR)
99
LI-COR fluorescence scanner
PCR amplification of <t>DNA</t> containing each of nine different microsatellites from each progeny plant with one of each locus-specific primer pairs, analysis of product mixtures <t>by</t> <t>capillary</t> electrophoresis, detection of fluorescent products, and generation of electropherograms were as described under “Materials and Methods.” A, Electropherograms showing all PCR products; one of each primer pair was labeled with FAM or HEX fluorescent dye. B, Representative electropherogram patterns for locus NGA1107. Apparent absolute size of primary wild-type (wt) product band is 317 bp. Shown also are products where both alleles showed an increase of one repeat unit, increasing apparent product length to 319 bp (+2), where one allele maintained wild-type length and one showed a loss of one repeat [wt & (-2)], and where one allele remained wild type and one showed a shift of two repeats, decreasing apparent length to 313 bp [wt & (-4)]. Arrows indicate position of 317-bp (wild-type) product. C, Patterns for reconstruction mixtures. DNA from plants homozygous (pure) for alleles at locus NGA1107 encoding 313-bp (black arrow) or 315-bp (gray arrow) products or mixtures of the two at indicated ratios (concentrations of DNAs measured before PCR by staining with PicoGreen [Molecular Probes, Eugene, OR]) were analyzed as described above. Note that the primary criterion for scoring a pattern as reflecting a mixture of two different length products—second peak from right greater than a significantly large first peak—is met only for 1:1 and 2:1 mixtures.
Fluorescence Scanner, supplied by LI-COR, 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/product/fluorescent+band+intensity/Odyssey+CLx+Imaging+System/pmc06420783-180-10-14
Average 99 stars, based on 1 article reviews
fluorescence scanner - by Bioz Stars, 2026-10
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band  (LI-COR)
99
LI-COR band
PCR amplification of <t>DNA</t> containing each of nine different microsatellites from each progeny plant with one of each locus-specific primer pairs, analysis of product mixtures <t>by</t> <t>capillary</t> electrophoresis, detection of fluorescent products, and generation of electropherograms were as described under “Materials and Methods.” A, Electropherograms showing all PCR products; one of each primer pair was labeled with FAM or HEX fluorescent dye. B, Representative electropherogram patterns for locus NGA1107. Apparent absolute size of primary wild-type (wt) product band is 317 bp. Shown also are products where both alleles showed an increase of one repeat unit, increasing apparent product length to 319 bp (+2), where one allele maintained wild-type length and one showed a loss of one repeat [wt & (-2)], and where one allele remained wild type and one showed a shift of two repeats, decreasing apparent length to 313 bp [wt & (-4)]. Arrows indicate position of 317-bp (wild-type) product. C, Patterns for reconstruction mixtures. DNA from plants homozygous (pure) for alleles at locus NGA1107 encoding 313-bp (black arrow) or 315-bp (gray arrow) products or mixtures of the two at indicated ratios (concentrations of DNAs measured before PCR by staining with PicoGreen [Molecular Probes, Eugene, OR]) were analyzed as described above. Note that the primary criterion for scoring a pattern as reflecting a mixture of two different length products—second peak from right greater than a significantly large first peak—is met only for 1:1 and 2:1 mixtures.
Band, supplied by LI-COR, 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/product/fluorescent+band+intensity/Pearl+Trilogy+Small+Animal+Imager/pmc09258243-65-4-11
Average 99 stars, based on 1 article reviews
band - by Bioz Stars, 2026-10
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li cor image studio software  (LI-COR)
98
LI-COR li cor image studio software
PCR amplification of <t>DNA</t> containing each of nine different microsatellites from each progeny plant with one of each locus-specific primer pairs, analysis of product mixtures <t>by</t> <t>capillary</t> electrophoresis, detection of fluorescent products, and generation of electropherograms were as described under “Materials and Methods.” A, Electropherograms showing all PCR products; one of each primer pair was labeled with FAM or HEX fluorescent dye. B, Representative electropherogram patterns for locus NGA1107. Apparent absolute size of primary wild-type (wt) product band is 317 bp. Shown also are products where both alleles showed an increase of one repeat unit, increasing apparent product length to 319 bp (+2), where one allele maintained wild-type length and one showed a loss of one repeat [wt & (-2)], and where one allele remained wild type and one showed a shift of two repeats, decreasing apparent length to 313 bp [wt & (-4)]. Arrows indicate position of 317-bp (wild-type) product. C, Patterns for reconstruction mixtures. DNA from plants homozygous (pure) for alleles at locus NGA1107 encoding 313-bp (black arrow) or 315-bp (gray arrow) products or mixtures of the two at indicated ratios (concentrations of DNAs measured before PCR by staining with PicoGreen [Molecular Probes, Eugene, OR]) were analyzed as described above. Note that the primary criterion for scoring a pattern as reflecting a mixture of two different length products—second peak from right greater than a significantly large first peak—is met only for 1:1 and 2:1 mixtures.
Li Cor Image Studio Software, supplied by LI-COR, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fluorescent+band+intensity/Fc+IMAGE+STUDIO+SOFTWARE/pmc06438763-123-10-10
Average 98 stars, based on 1 article reviews
li cor image studio software - by Bioz Stars, 2026-10
98/100 stars
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sds page gels  (Bio-Rad)
98
Bio-Rad sds page gels
PCR amplification of <t>DNA</t> containing each of nine different microsatellites from each progeny plant with one of each locus-specific primer pairs, analysis of product mixtures <t>by</t> <t>capillary</t> electrophoresis, detection of fluorescent products, and generation of electropherograms were as described under “Materials and Methods.” A, Electropherograms showing all PCR products; one of each primer pair was labeled with FAM or HEX fluorescent dye. B, Representative electropherogram patterns for locus NGA1107. Apparent absolute size of primary wild-type (wt) product band is 317 bp. Shown also are products where both alleles showed an increase of one repeat unit, increasing apparent product length to 319 bp (+2), where one allele maintained wild-type length and one showed a loss of one repeat [wt & (-2)], and where one allele remained wild type and one showed a shift of two repeats, decreasing apparent length to 313 bp [wt & (-4)]. Arrows indicate position of 317-bp (wild-type) product. C, Patterns for reconstruction mixtures. DNA from plants homozygous (pure) for alleles at locus NGA1107 encoding 313-bp (black arrow) or 315-bp (gray arrow) products or mixtures of the two at indicated ratios (concentrations of DNAs measured before PCR by staining with PicoGreen [Molecular Probes, Eugene, OR]) were analyzed as described above. Note that the primary criterion for scoring a pattern as reflecting a mixture of two different length products—second peak from right greater than a significantly large first peak—is met only for 1:1 and 2:1 mixtures.
Sds Page Gels, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fluorescent+band+intensity/SDS/us11684676-913-6-13
Average 98 stars, based on 1 article reviews
sds page gels - by Bioz Stars, 2026-10
98/100 stars
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snarf-1 fluorescence bands  (OriginLab corp)
90
OriginLab corp snarf-1 fluorescence bands
PCR amplification of <t>DNA</t> containing each of nine different microsatellites from each progeny plant with one of each locus-specific primer pairs, analysis of product mixtures <t>by</t> <t>capillary</t> electrophoresis, detection of fluorescent products, and generation of electropherograms were as described under “Materials and Methods.” A, Electropherograms showing all PCR products; one of each primer pair was labeled with FAM or HEX fluorescent dye. B, Representative electropherogram patterns for locus NGA1107. Apparent absolute size of primary wild-type (wt) product band is 317 bp. Shown also are products where both alleles showed an increase of one repeat unit, increasing apparent product length to 319 bp (+2), where one allele maintained wild-type length and one showed a loss of one repeat [wt & (-2)], and where one allele remained wild type and one showed a shift of two repeats, decreasing apparent length to 313 bp [wt & (-4)]. Arrows indicate position of 317-bp (wild-type) product. C, Patterns for reconstruction mixtures. DNA from plants homozygous (pure) for alleles at locus NGA1107 encoding 313-bp (black arrow) or 315-bp (gray arrow) products or mixtures of the two at indicated ratios (concentrations of DNAs measured before PCR by staining with PicoGreen [Molecular Probes, Eugene, OR]) were analyzed as described above. Note that the primary criterion for scoring a pattern as reflecting a mixture of two different length products—second peak from right greater than a significantly large first peak—is met only for 1:1 and 2:1 mixtures.
Snarf 1 Fluorescence Bands, supplied by OriginLab corp, 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/fluorescent+band+intensity/snarf+1+fluorescence+bands/pm30351149-201-10-16
Average 90 stars, based on 1 article reviews
snarf-1 fluorescence bands - by Bioz Stars, 2026-10
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quantity one quantitation software  (Bio-Rad)
96
Bio-Rad quantity one quantitation software
PCR amplification of <t>DNA</t> containing each of nine different microsatellites from each progeny plant with one of each locus-specific primer pairs, analysis of product mixtures <t>by</t> <t>capillary</t> electrophoresis, detection of fluorescent products, and generation of electropherograms were as described under “Materials and Methods.” A, Electropherograms showing all PCR products; one of each primer pair was labeled with FAM or HEX fluorescent dye. B, Representative electropherogram patterns for locus NGA1107. Apparent absolute size of primary wild-type (wt) product band is 317 bp. Shown also are products where both alleles showed an increase of one repeat unit, increasing apparent product length to 319 bp (+2), where one allele maintained wild-type length and one showed a loss of one repeat [wt & (-2)], and where one allele remained wild type and one showed a shift of two repeats, decreasing apparent length to 313 bp [wt & (-4)]. Arrows indicate position of 317-bp (wild-type) product. C, Patterns for reconstruction mixtures. DNA from plants homozygous (pure) for alleles at locus NGA1107 encoding 313-bp (black arrow) or 315-bp (gray arrow) products or mixtures of the two at indicated ratios (concentrations of DNAs measured before PCR by staining with PicoGreen [Molecular Probes, Eugene, OR]) were analyzed as described above. Note that the primary criterion for scoring a pattern as reflecting a mixture of two different length products—second peak from right greater than a significantly large first peak—is met only for 1:1 and 2:1 mixtures.
Quantity One Quantitation Software, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fluorescent+band+intensity/ChromLab+Software/pmc03549469-227-8-12
Average 96 stars, based on 1 article reviews
quantity one quantitation software - by Bioz Stars, 2026-10
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image analyzer argus-100  (Hamamatsu)
90
Hamamatsu image analyzer argus-100
PCR amplification of <t>DNA</t> containing each of nine different microsatellites from each progeny plant with one of each locus-specific primer pairs, analysis of product mixtures <t>by</t> <t>capillary</t> electrophoresis, detection of fluorescent products, and generation of electropherograms were as described under “Materials and Methods.” A, Electropherograms showing all PCR products; one of each primer pair was labeled with FAM or HEX fluorescent dye. B, Representative electropherogram patterns for locus NGA1107. Apparent absolute size of primary wild-type (wt) product band is 317 bp. Shown also are products where both alleles showed an increase of one repeat unit, increasing apparent product length to 319 bp (+2), where one allele maintained wild-type length and one showed a loss of one repeat [wt & (-2)], and where one allele remained wild type and one showed a shift of two repeats, decreasing apparent length to 313 bp [wt & (-4)]. Arrows indicate position of 317-bp (wild-type) product. C, Patterns for reconstruction mixtures. DNA from plants homozygous (pure) for alleles at locus NGA1107 encoding 313-bp (black arrow) or 315-bp (gray arrow) products or mixtures of the two at indicated ratios (concentrations of DNAs measured before PCR by staining with PicoGreen [Molecular Probes, Eugene, OR]) were analyzed as described above. Note that the primary criterion for scoring a pattern as reflecting a mixture of two different length products—second peak from right greater than a significantly large first peak—is met only for 1:1 and 2:1 mixtures.
Image Analyzer Argus 100, supplied by Hamamatsu, 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/fluorescent+band+intensity/argus+100/pm11836782-174-8-11
Average 90 stars, based on 1 article reviews
image analyzer argus-100 - by Bioz Stars, 2026-10
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clinx chemiscope imaging system  (Clinx Science)
96
Clinx Science clinx chemiscope imaging system
PCR amplification of <t>DNA</t> containing each of nine different microsatellites from each progeny plant with one of each locus-specific primer pairs, analysis of product mixtures <t>by</t> <t>capillary</t> electrophoresis, detection of fluorescent products, and generation of electropherograms were as described under “Materials and Methods.” A, Electropherograms showing all PCR products; one of each primer pair was labeled with FAM or HEX fluorescent dye. B, Representative electropherogram patterns for locus NGA1107. Apparent absolute size of primary wild-type (wt) product band is 317 bp. Shown also are products where both alleles showed an increase of one repeat unit, increasing apparent product length to 319 bp (+2), where one allele maintained wild-type length and one showed a loss of one repeat [wt & (-2)], and where one allele remained wild type and one showed a shift of two repeats, decreasing apparent length to 313 bp [wt & (-4)]. Arrows indicate position of 317-bp (wild-type) product. C, Patterns for reconstruction mixtures. DNA from plants homozygous (pure) for alleles at locus NGA1107 encoding 313-bp (black arrow) or 315-bp (gray arrow) products or mixtures of the two at indicated ratios (concentrations of DNAs measured before PCR by staining with PicoGreen [Molecular Probes, Eugene, OR]) were analyzed as described above. Note that the primary criterion for scoring a pattern as reflecting a mixture of two different length products—second peak from right greater than a significantly large first peak—is met only for 1:1 and 2:1 mixtures.
Clinx Chemiscope Imaging System, supplied by Clinx Science, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fluorescent+band+intensity/ChemiScope+6100+chemiluminescence+and+fluorescence+imaging+system/pm27644038-82-10-10
Average 96 stars, based on 1 article reviews
clinx chemiscope imaging system - by Bioz Stars, 2026-10
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Image Search Results


PCR amplification of DNA containing each of nine different microsatellites from each progeny plant with one of each locus-specific primer pairs, analysis of product mixtures by capillary electrophoresis, detection of fluorescent products, and generation of electropherograms were as described under “Materials and Methods.” A, Electropherograms showing all PCR products; one of each primer pair was labeled with FAM or HEX fluorescent dye. B, Representative electropherogram patterns for locus NGA1107. Apparent absolute size of primary wild-type (wt) product band is 317 bp. Shown also are products where both alleles showed an increase of one repeat unit, increasing apparent product length to 319 bp (+2), where one allele maintained wild-type length and one showed a loss of one repeat [wt & (-2)], and where one allele remained wild type and one showed a shift of two repeats, decreasing apparent length to 313 bp [wt & (-4)]. Arrows indicate position of 317-bp (wild-type) product. C, Patterns for reconstruction mixtures. DNA from plants homozygous (pure) for alleles at locus NGA1107 encoding 313-bp (black arrow) or 315-bp (gray arrow) products or mixtures of the two at indicated ratios (concentrations of DNAs measured before PCR by staining with PicoGreen [Molecular Probes, Eugene, OR]) were analyzed as described above. Note that the primary criterion for scoring a pattern as reflecting a mixture of two different length products—second peak from right greater than a significantly large first peak—is met only for 1:1 and 2:1 mixtures.

Journal:

Article Title: Reduction of Stability of Arabidopsis Genomic and Transgenic DNA-Repeat Sequences (Microsatellites) by Inactivation of AtMSH2 Mismatch-Repair Function 1

doi: 10.1104/pp.103.023952

Figure Lengend Snippet: PCR amplification of DNA containing each of nine different microsatellites from each progeny plant with one of each locus-specific primer pairs, analysis of product mixtures by capillary electrophoresis, detection of fluorescent products, and generation of electropherograms were as described under “Materials and Methods.” A, Electropherograms showing all PCR products; one of each primer pair was labeled with FAM or HEX fluorescent dye. B, Representative electropherogram patterns for locus NGA1107. Apparent absolute size of primary wild-type (wt) product band is 317 bp. Shown also are products where both alleles showed an increase of one repeat unit, increasing apparent product length to 319 bp (+2), where one allele maintained wild-type length and one showed a loss of one repeat [wt & (-2)], and where one allele remained wild type and one showed a shift of two repeats, decreasing apparent length to 313 bp [wt & (-4)]. Arrows indicate position of 317-bp (wild-type) product. C, Patterns for reconstruction mixtures. DNA from plants homozygous (pure) for alleles at locus NGA1107 encoding 313-bp (black arrow) or 315-bp (gray arrow) products or mixtures of the two at indicated ratios (concentrations of DNAs measured before PCR by staining with PicoGreen [Molecular Probes, Eugene, OR]) were analyzed as described above. Note that the primary criterion for scoring a pattern as reflecting a mixture of two different length products—second peak from right greater than a significantly large first peak—is met only for 1:1 and 2:1 mixtures.

Article Snippet: Up to nine locus-specific PCR reaction products were diluted as empirically found appropriate for subsequent analysis, mixed, and analyzed by capillary electrophoresis and measurement of DNA-band fluorescent intensities, using the ABI Prism 3100 Genetic Analyzer and associated software (Applied Biosystems, Palo Alto, CA).

Techniques: Amplification, Electrophoresis, Labeling, Staining