base pair fragment Search Results


840-base pair fragment from human erdj3  (Incyte corporation)
90
Incyte corporation 840-base pair fragment from human erdj3
840 Base Pair Fragment From Human Erdj3, supplied by Incyte corporation, 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/840-base pair fragment from human erdj3/product/Incyte corporation
Average 90 stars, based on 1 article reviews
840-base pair fragment from human erdj3 - by Bioz Stars, 2026-06
90/100 stars
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synthetic 751-base pair fragment  (GenScript corporation)
90
GenScript corporation synthetic 751-base pair fragment
Synthetic 751 Base Pair Fragment, supplied by GenScript corporation, 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/synthetic 751-base pair fragment/product/GenScript corporation
Average 90 stars, based on 1 article reviews
synthetic 751-base pair fragment - by Bioz Stars, 2026-06
90/100 stars
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1516-base pair fragment of the mouse glp-2r gene  (Incyte corporation)
90
Incyte corporation 1516-base pair fragment of the mouse glp-2r gene
1516 Base Pair Fragment Of The Mouse Glp 2r Gene, supplied by Incyte corporation, 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/1516-base pair fragment of the mouse glp-2r gene/product/Incyte corporation
Average 90 stars, based on 1 article reviews
1516-base pair fragment of the mouse glp-2r gene - by Bioz Stars, 2026-06
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1108-base pair ecori fragment of the tnfa cdna  (Genentech inc)
90
Genentech inc 1108-base pair ecori fragment of the tnfa cdna
1108 Base Pair Ecori Fragment Of The Tnfa Cdna, supplied by Genentech 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/1108-base pair ecori fragment of the tnfa cdna/product/Genentech inc
Average 90 stars, based on 1 article reviews
1108-base pair ecori fragment of the tnfa cdna - by Bioz Stars, 2026-06
90/100 stars
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402 base pair fragment of human ahr cdna  (Promega)
90
Promega 402 base pair fragment of human ahr cdna
402 Base Pair Fragment Of Human Ahr Cdna, supplied by Promega, 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/402 base pair fragment of human ahr cdna/product/Promega
Average 90 stars, based on 1 article reviews
402 base pair fragment of human ahr cdna - by Bioz Stars, 2026-06
90/100 stars
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gene fragment coding for residues 712–914 (base pair 2444–3055) of human α -actinin 1  (GenScript corporation)
90
GenScript corporation gene fragment coding for residues 712–914 (base pair 2444–3055) of human α -actinin 1
Gene Fragment Coding For Residues 712–914 (Base Pair 2444–3055) Of Human α Actinin 1, supplied by GenScript corporation, 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/gene fragment coding for residues 712–914 (base pair 2444–3055) of human α -actinin 1/product/GenScript corporation
Average 90 stars, based on 1 article reviews
gene fragment coding for residues 712–914 (base pair 2444–3055) of human α -actinin 1 - by Bioz Stars, 2026-06
90/100 stars
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gblocks fragment containing 5 sgrna expression cassettes with high fidelity four-base overhang pair  (GenScript corporation)
90
GenScript corporation gblocks fragment containing 5 sgrna expression cassettes with high fidelity four-base overhang pair
a, Framework for converting TAG codons into TAA in human cells. b, UAGs number and editable UAG sites of all genes and essential genes in each chromosome. c-e, distribution analysis of cells with different number of modified gene targets in populations with different delivery methods based on single cell RNAseq. Method_1, delivery 10 <t>gBlocks</t> with mCherry-inactivated eGFP reporter; Method_2, delivery 10 gBlocks with mCherry-inactivated eGFP reporter and <t>eGFP</t> <t>sgRNA</t> plasmids; Method_3, delivery 43-all-in-one with DsRed. f, Density plot for distribution of number of modified gene targets detected by scRNAseq in 3 populations. Vertical lines indicate the median values of modified gene targets. g, For each gene target, distribution analysis of modified cells with different editing efficiency. Counts from different methods were stacked in the plot. h, Editing efficiency of each sgRNAs in single cells. i, Heat map of target “C” editing efficiency in cell population with three delivery methods based on converting single-cell RNA-Seq into Bulk RNA-Seq. Editing efficiency was indicated with the intensity of red.
Gblocks Fragment Containing 5 Sgrna Expression Cassettes With High Fidelity Four Base Overhang Pair, supplied by GenScript corporation, 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/gblocks fragment containing 5 sgrna expression cassettes with high fidelity four-base overhang pair/product/GenScript corporation
Average 90 stars, based on 1 article reviews
gblocks fragment containing 5 sgrna expression cassettes with high fidelity four-base overhang pair - by Bioz Stars, 2026-06
90/100 stars
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208 base pair fragment  (Maxim Biotech Inc)
90
Maxim Biotech Inc 208 base pair fragment
a, Framework for converting TAG codons into TAA in human cells. b, UAGs number and editable UAG sites of all genes and essential genes in each chromosome. c-e, distribution analysis of cells with different number of modified gene targets in populations with different delivery methods based on single cell RNAseq. Method_1, delivery 10 <t>gBlocks</t> with mCherry-inactivated eGFP reporter; Method_2, delivery 10 gBlocks with mCherry-inactivated eGFP reporter and <t>eGFP</t> <t>sgRNA</t> plasmids; Method_3, delivery 43-all-in-one with DsRed. f, Density plot for distribution of number of modified gene targets detected by scRNAseq in 3 populations. Vertical lines indicate the median values of modified gene targets. g, For each gene target, distribution analysis of modified cells with different editing efficiency. Counts from different methods were stacked in the plot. h, Editing efficiency of each sgRNAs in single cells. i, Heat map of target “C” editing efficiency in cell population with three delivery methods based on converting single-cell RNA-Seq into Bulk RNA-Seq. Editing efficiency was indicated with the intensity of red.
208 Base Pair Fragment, supplied by Maxim Biotech 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/208 base pair fragment/product/Maxim Biotech Inc
Average 90 stars, based on 1 article reviews
208 base pair fragment - by Bioz Stars, 2026-06
90/100 stars
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600 base pair bam hi/bam hi fragment to ed-il4  (DiscoverX corporation)
90
DiscoverX corporation 600 base pair bam hi/bam hi fragment to ed-il4
a, Framework for converting TAG codons into TAA in human cells. b, UAGs number and editable UAG sites of all genes and essential genes in each chromosome. c-e, distribution analysis of cells with different number of modified gene targets in populations with different delivery methods based on single cell RNAseq. Method_1, delivery 10 <t>gBlocks</t> with mCherry-inactivated eGFP reporter; Method_2, delivery 10 gBlocks with mCherry-inactivated eGFP reporter and <t>eGFP</t> <t>sgRNA</t> plasmids; Method_3, delivery 43-all-in-one with DsRed. f, Density plot for distribution of number of modified gene targets detected by scRNAseq in 3 populations. Vertical lines indicate the median values of modified gene targets. g, For each gene target, distribution analysis of modified cells with different editing efficiency. Counts from different methods were stacked in the plot. h, Editing efficiency of each sgRNAs in single cells. i, Heat map of target “C” editing efficiency in cell population with three delivery methods based on converting single-cell RNA-Seq into Bulk RNA-Seq. Editing efficiency was indicated with the intensity of red.
600 Base Pair Bam Hi/Bam Hi Fragment To Ed Il4, supplied by DiscoverX corporation, 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/600 base pair bam hi/bam hi fragment to ed-il4/product/DiscoverX corporation
Average 90 stars, based on 1 article reviews
600 base pair bam hi/bam hi fragment to ed-il4 - by Bioz Stars, 2026-06
90/100 stars
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82 base pair fragment  (Active Motif)
90
Active Motif 82 base pair fragment
a, Framework for converting TAG codons into TAA in human cells. b, UAGs number and editable UAG sites of all genes and essential genes in each chromosome. c-e, distribution analysis of cells with different number of modified gene targets in populations with different delivery methods based on single cell RNAseq. Method_1, delivery 10 <t>gBlocks</t> with mCherry-inactivated eGFP reporter; Method_2, delivery 10 gBlocks with mCherry-inactivated eGFP reporter and <t>eGFP</t> <t>sgRNA</t> plasmids; Method_3, delivery 43-all-in-one with DsRed. f, Density plot for distribution of number of modified gene targets detected by scRNAseq in 3 populations. Vertical lines indicate the median values of modified gene targets. g, For each gene target, distribution analysis of modified cells with different editing efficiency. Counts from different methods were stacked in the plot. h, Editing efficiency of each sgRNAs in single cells. i, Heat map of target “C” editing efficiency in cell population with three delivery methods based on converting single-cell RNA-Seq into Bulk RNA-Seq. Editing efficiency was indicated with the intensity of red.
82 Base Pair Fragment, supplied by Active Motif, 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/82 base pair fragment/product/Active Motif
Average 90 stars, based on 1 article reviews
82 base pair fragment - by Bioz Stars, 2026-06
90/100 stars
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0.57 ng of a gel-purified 43-base pair dna fragment  (Promega)
90
Promega 0.57 ng of a gel-purified 43-base pair dna fragment
a, Framework for converting TAG codons into TAA in human cells. b, UAGs number and editable UAG sites of all genes and essential genes in each chromosome. c-e, distribution analysis of cells with different number of modified gene targets in populations with different delivery methods based on single cell RNAseq. Method_1, delivery 10 <t>gBlocks</t> with mCherry-inactivated eGFP reporter; Method_2, delivery 10 gBlocks with mCherry-inactivated eGFP reporter and <t>eGFP</t> <t>sgRNA</t> plasmids; Method_3, delivery 43-all-in-one with DsRed. f, Density plot for distribution of number of modified gene targets detected by scRNAseq in 3 populations. Vertical lines indicate the median values of modified gene targets. g, For each gene target, distribution analysis of modified cells with different editing efficiency. Counts from different methods were stacked in the plot. h, Editing efficiency of each sgRNAs in single cells. i, Heat map of target “C” editing efficiency in cell population with three delivery methods based on converting single-cell RNA-Seq into Bulk RNA-Seq. Editing efficiency was indicated with the intensity of red.
0.57 Ng Of A Gel Purified 43 Base Pair Dna Fragment, supplied by Promega, 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/0.57 ng of a gel-purified 43-base pair dna fragment/product/Promega
Average 90 stars, based on 1 article reviews
0.57 ng of a gel-purified 43-base pair dna fragment - by Bioz Stars, 2026-06
90/100 stars
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150 base-pair linear dna fragment containing the mtb rrnap3 promoter  (National Institute of Standards and Technology)
90
National Institute of Standards and Technology 150 base-pair linear dna fragment containing the mtb rrnap3 promoter
a, Framework for converting TAG codons into TAA in human cells. b, UAGs number and editable UAG sites of all genes and essential genes in each chromosome. c-e, distribution analysis of cells with different number of modified gene targets in populations with different delivery methods based on single cell RNAseq. Method_1, delivery 10 <t>gBlocks</t> with mCherry-inactivated eGFP reporter; Method_2, delivery 10 gBlocks with mCherry-inactivated eGFP reporter and <t>eGFP</t> <t>sgRNA</t> plasmids; Method_3, delivery 43-all-in-one with DsRed. f, Density plot for distribution of number of modified gene targets detected by scRNAseq in 3 populations. Vertical lines indicate the median values of modified gene targets. g, For each gene target, distribution analysis of modified cells with different editing efficiency. Counts from different methods were stacked in the plot. h, Editing efficiency of each sgRNAs in single cells. i, Heat map of target “C” editing efficiency in cell population with three delivery methods based on converting single-cell RNA-Seq into Bulk RNA-Seq. Editing efficiency was indicated with the intensity of red.
150 Base Pair Linear Dna Fragment Containing The Mtb Rrnap3 Promoter, supplied by National Institute of Standards and Technology, 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/150 base-pair linear dna fragment containing the mtb rrnap3 promoter/product/National Institute of Standards and Technology
Average 90 stars, based on 1 article reviews
150 base-pair linear dna fragment containing the mtb rrnap3 promoter - by Bioz Stars, 2026-06
90/100 stars
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Image Search Results


a, Framework for converting TAG codons into TAA in human cells. b, UAGs number and editable UAG sites of all genes and essential genes in each chromosome. c-e, distribution analysis of cells with different number of modified gene targets in populations with different delivery methods based on single cell RNAseq. Method_1, delivery 10 gBlocks with mCherry-inactivated eGFP reporter; Method_2, delivery 10 gBlocks with mCherry-inactivated eGFP reporter and eGFP sgRNA plasmids; Method_3, delivery 43-all-in-one with DsRed. f, Density plot for distribution of number of modified gene targets detected by scRNAseq in 3 populations. Vertical lines indicate the median values of modified gene targets. g, For each gene target, distribution analysis of modified cells with different editing efficiency. Counts from different methods were stacked in the plot. h, Editing efficiency of each sgRNAs in single cells. i, Heat map of target “C” editing efficiency in cell population with three delivery methods based on converting single-cell RNA-Seq into Bulk RNA-Seq. Editing efficiency was indicated with the intensity of red.

Journal: bioRxiv

Article Title: Multiplex base editing to convert TAG into TAA codons in the human genome

doi: 10.1101/2021.07.13.452007

Figure Lengend Snippet: a, Framework for converting TAG codons into TAA in human cells. b, UAGs number and editable UAG sites of all genes and essential genes in each chromosome. c-e, distribution analysis of cells with different number of modified gene targets in populations with different delivery methods based on single cell RNAseq. Method_1, delivery 10 gBlocks with mCherry-inactivated eGFP reporter; Method_2, delivery 10 gBlocks with mCherry-inactivated eGFP reporter and eGFP sgRNA plasmids; Method_3, delivery 43-all-in-one with DsRed. f, Density plot for distribution of number of modified gene targets detected by scRNAseq in 3 populations. Vertical lines indicate the median values of modified gene targets. g, For each gene target, distribution analysis of modified cells with different editing efficiency. Counts from different methods were stacked in the plot. h, Editing efficiency of each sgRNAs in single cells. i, Heat map of target “C” editing efficiency in cell population with three delivery methods based on converting single-cell RNA-Seq into Bulk RNA-Seq. Editing efficiency was indicated with the intensity of red.

Article Snippet: All gBlocks fragment containing 5 sgRNA expression cassettes with high fidelity four-base overhang pair after cutting with type IIS restriction enzyme BbsI restriction enzyme were designed and directly sent to be synthesized into PUC57 cloning plasmid by GenScript.

Techniques: Modification, RNA Sequencing