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orange dna loading dye  (Thermo Fisher)


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    Structured Review

    Thermo Fisher orange dna loading dye
    Polymerase chain reaction detection of breakpoint region in (A) 19Q4–77 wx and RTx430 and (B) 19Q4–94 Wx and RTx430 and Integrative Genome Viewer screenshot of contiguous assemblies of 19Q4–77 wx , 19Q4–94 Wx , and RTx430 reads at and around the ~400-kb deletion in k1C family (C) . Top row depicts amplification of unedited genome using primer set in deleted region (716 bp), and bottom row depicts amplification of junction fragment from edited genome using primer set that spans deletion (780 bp). First and last lanes of each row contain a 1-kb ladder. Lanes 2–14 for top and bottom rows contain <t>DNA</t> from 19Q4–77 wx (A) and 19Q4–94 Wx (B) plants, with lanes 17–19 containing DNA from unedited RTx430 plants (both).
    Orange Dna Loading Dye, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 201 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/orange dna loading dye/product/Thermo Fisher
    Average 95 stars, based on 201 article reviews
    orange dna loading dye - by Bioz Stars, 2026-03
    95/100 stars

    Images

    1) Product Images from "Large scale deletion and rebalancing within the k1C kafirin family in sorghum"

    Article Title: Large scale deletion and rebalancing within the k1C kafirin family in sorghum

    Journal: Frontiers in Plant Science

    doi: 10.3389/fpls.2025.1686027

    Polymerase chain reaction detection of breakpoint region in (A) 19Q4–77 wx and RTx430 and (B) 19Q4–94 Wx and RTx430 and Integrative Genome Viewer screenshot of contiguous assemblies of 19Q4–77 wx , 19Q4–94 Wx , and RTx430 reads at and around the ~400-kb deletion in k1C family (C) . Top row depicts amplification of unedited genome using primer set in deleted region (716 bp), and bottom row depicts amplification of junction fragment from edited genome using primer set that spans deletion (780 bp). First and last lanes of each row contain a 1-kb ladder. Lanes 2–14 for top and bottom rows contain DNA from 19Q4–77 wx (A) and 19Q4–94 Wx (B) plants, with lanes 17–19 containing DNA from unedited RTx430 plants (both).
    Figure Legend Snippet: Polymerase chain reaction detection of breakpoint region in (A) 19Q4–77 wx and RTx430 and (B) 19Q4–94 Wx and RTx430 and Integrative Genome Viewer screenshot of contiguous assemblies of 19Q4–77 wx , 19Q4–94 Wx , and RTx430 reads at and around the ~400-kb deletion in k1C family (C) . Top row depicts amplification of unedited genome using primer set in deleted region (716 bp), and bottom row depicts amplification of junction fragment from edited genome using primer set that spans deletion (780 bp). First and last lanes of each row contain a 1-kb ladder. Lanes 2–14 for top and bottom rows contain DNA from 19Q4–77 wx (A) and 19Q4–94 Wx (B) plants, with lanes 17–19 containing DNA from unedited RTx430 plants (both).

    Techniques Used: Polymerase Chain Reaction, Amplification



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    orange dna loading dye  (Thermo Fisher)
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    Thermo Fisher orange dna loading dye
    Polymerase chain reaction detection of breakpoint region in (A) 19Q4–77 wx and RTx430 and (B) 19Q4–94 Wx and RTx430 and Integrative Genome Viewer screenshot of contiguous assemblies of 19Q4–77 wx , 19Q4–94 Wx , and RTx430 reads at and around the ~400-kb deletion in k1C family (C) . Top row depicts amplification of unedited genome using primer set in deleted region (716 bp), and bottom row depicts amplification of junction fragment from edited genome using primer set that spans deletion (780 bp). First and last lanes of each row contain a 1-kb ladder. Lanes 2–14 for top and bottom rows contain <t>DNA</t> from 19Q4–77 wx (A) and 19Q4–94 Wx (B) plants, with lanes 17–19 containing DNA from unedited RTx430 plants (both).
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    https://www.bioz.com/result/orange dna loading dye/product/Thermo Fisher
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    orange dna loading dye 6x  (Thermo Fisher)
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    Polymerase chain reaction detection of breakpoint region in (A) 19Q4–77 wx and RTx430 and (B) 19Q4–94 Wx and RTx430 and Integrative Genome Viewer screenshot of contiguous assemblies of 19Q4–77 wx , 19Q4–94 Wx , and RTx430 reads at and around the ~400-kb deletion in k1C family (C) . Top row depicts amplification of unedited genome using primer set in deleted region (716 bp), and bottom row depicts amplification of junction fragment from edited genome using primer set that spans deletion (780 bp). First and last lanes of each row contain a 1-kb ladder. Lanes 2–14 for top and bottom rows contain <t>DNA</t> from 19Q4–77 wx (A) and 19Q4–94 Wx (B) plants, with lanes 17–19 containing DNA from unedited RTx430 plants (both).
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    Image Search Results


    Polymerase chain reaction detection of breakpoint region in (A) 19Q4–77 wx and RTx430 and (B) 19Q4–94 Wx and RTx430 and Integrative Genome Viewer screenshot of contiguous assemblies of 19Q4–77 wx , 19Q4–94 Wx , and RTx430 reads at and around the ~400-kb deletion in k1C family (C) . Top row depicts amplification of unedited genome using primer set in deleted region (716 bp), and bottom row depicts amplification of junction fragment from edited genome using primer set that spans deletion (780 bp). First and last lanes of each row contain a 1-kb ladder. Lanes 2–14 for top and bottom rows contain DNA from 19Q4–77 wx (A) and 19Q4–94 Wx (B) plants, with lanes 17–19 containing DNA from unedited RTx430 plants (both).

    Journal: Frontiers in Plant Science

    Article Title: Large scale deletion and rebalancing within the k1C kafirin family in sorghum

    doi: 10.3389/fpls.2025.1686027

    Figure Lengend Snippet: Polymerase chain reaction detection of breakpoint region in (A) 19Q4–77 wx and RTx430 and (B) 19Q4–94 Wx and RTx430 and Integrative Genome Viewer screenshot of contiguous assemblies of 19Q4–77 wx , 19Q4–94 Wx , and RTx430 reads at and around the ~400-kb deletion in k1C family (C) . Top row depicts amplification of unedited genome using primer set in deleted region (716 bp), and bottom row depicts amplification of junction fragment from edited genome using primer set that spans deletion (780 bp). First and last lanes of each row contain a 1-kb ladder. Lanes 2–14 for top and bottom rows contain DNA from 19Q4–77 wx (A) and 19Q4–94 Wx (B) plants, with lanes 17–19 containing DNA from unedited RTx430 plants (both).

    Article Snippet: PCR products were combined with Orange DNA Loading Dye (Thermo Fisher; Catalog no. R0631: Massachusetts, United States) and loaded onto 1%–2% agarose gels stained with ethidium bromide.

    Techniques: Polymerase Chain Reaction, Amplification