3 desthiobiotin teg guanosine 5 triphosphate dtbgtp  (New England Biolabs)


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    New England Biolabs 3 desthiobiotin gtp dtb gtp
    ReCappable-seq. (A) Principle of ReCappable-seq. (1) RNA is subjected to decapping with yDcpS, which acts on capped transcripts originating from Pol II transcription. Subsequently, the RNA is capped with a biotin-modified GTP analog <t>(3′-desthiobiotin-GTP)</t> using VCE. This biotinylation step allows enrichment of all primary transcripts on a streptavidin matrix. (2) Differentiation of Pol II from the non–Pol II transcripts is accomplished by sequencing a second library constructed with RNA treated with CIP before the yDcpS treatment, in order to remove the 5′ triphosphate from non–Pol II transcripts. (B) RT-qPCR assay measuring the recovery after streptavidin enrichment of various classes of transcripts such as RNA18S1 rRNA as an example of a processed transcript; ACTB, RPL19, MALAT1, FKBP5, TMSB10, H3C10, and HIST2H3B as examples of capped transcripts; RMRP, RPPH1, and RN7SK as examples of Pol III transcripts (with RN7SK having a 5′ methylated triphosphate and therefore being resistant to CIP treatment; see main text); and ERCC190 and FLUC as examples of spiked-in in vitro transcripts with a defined triphosphorylated 5′ end. The Cq values are available in Supplemental Figure S1F. (C) Example of a Pol II TSS in the TMSB10 locus: The same positions (shaded in pink) are found in the CAGE data set. CIP treatment intensifies the signal, consistent with a Pol II TSS. (D) Example of Pol III TSS corresponding to the start of two vault RNAs (vtRNA1-1 and vtRNA1-2) located on Chr 5. The positions (shaded in pink) are missing in the CAGE data set. CIP treatment reduces the signal, consistent with non–Pol II TSS. In C and D, the tracks correspond to ReCappable-seq, CIP-ReCappable-seq, and CAGE read coverage (number of reads). All libraries were down-sampled to the same number of total mapped reads (63,300,000) to facilitate comparison. The four bottom tracks correspond to read density from public ENCODE DNase-seq from A549 cells (ENCFF473YHH, ENCFF809KIH, ENCFF821UUL, ENCFF961WXW).
    3 Desthiobiotin Gtp Dtb Gtp, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Comprehensive determination of transcription start sites derived from all RNA polymerases using ReCappable-seq"

    Article Title: Comprehensive determination of transcription start sites derived from all RNA polymerases using ReCappable-seq

    Journal: Genome Research

    doi: 10.1101/gr.275784.121

    ReCappable-seq. (A) Principle of ReCappable-seq. (1) RNA is subjected to decapping with yDcpS, which acts on capped transcripts originating from Pol II transcription. Subsequently, the RNA is capped with a biotin-modified GTP analog (3′-desthiobiotin-GTP) using VCE. This biotinylation step allows enrichment of all primary transcripts on a streptavidin matrix. (2) Differentiation of Pol II from the non–Pol II transcripts is accomplished by sequencing a second library constructed with RNA treated with CIP before the yDcpS treatment, in order to remove the 5′ triphosphate from non–Pol II transcripts. (B) RT-qPCR assay measuring the recovery after streptavidin enrichment of various classes of transcripts such as RNA18S1 rRNA as an example of a processed transcript; ACTB, RPL19, MALAT1, FKBP5, TMSB10, H3C10, and HIST2H3B as examples of capped transcripts; RMRP, RPPH1, and RN7SK as examples of Pol III transcripts (with RN7SK having a 5′ methylated triphosphate and therefore being resistant to CIP treatment; see main text); and ERCC190 and FLUC as examples of spiked-in in vitro transcripts with a defined triphosphorylated 5′ end. The Cq values are available in Supplemental Figure S1F. (C) Example of a Pol II TSS in the TMSB10 locus: The same positions (shaded in pink) are found in the CAGE data set. CIP treatment intensifies the signal, consistent with a Pol II TSS. (D) Example of Pol III TSS corresponding to the start of two vault RNAs (vtRNA1-1 and vtRNA1-2) located on Chr 5. The positions (shaded in pink) are missing in the CAGE data set. CIP treatment reduces the signal, consistent with non–Pol II TSS. In C and D, the tracks correspond to ReCappable-seq, CIP-ReCappable-seq, and CAGE read coverage (number of reads). All libraries were down-sampled to the same number of total mapped reads (63,300,000) to facilitate comparison. The four bottom tracks correspond to read density from public ENCODE DNase-seq from A549 cells (ENCFF473YHH, ENCFF809KIH, ENCFF821UUL, ENCFF961WXW).
    Figure Legend Snippet: ReCappable-seq. (A) Principle of ReCappable-seq. (1) RNA is subjected to decapping with yDcpS, which acts on capped transcripts originating from Pol II transcription. Subsequently, the RNA is capped with a biotin-modified GTP analog (3′-desthiobiotin-GTP) using VCE. This biotinylation step allows enrichment of all primary transcripts on a streptavidin matrix. (2) Differentiation of Pol II from the non–Pol II transcripts is accomplished by sequencing a second library constructed with RNA treated with CIP before the yDcpS treatment, in order to remove the 5′ triphosphate from non–Pol II transcripts. (B) RT-qPCR assay measuring the recovery after streptavidin enrichment of various classes of transcripts such as RNA18S1 rRNA as an example of a processed transcript; ACTB, RPL19, MALAT1, FKBP5, TMSB10, H3C10, and HIST2H3B as examples of capped transcripts; RMRP, RPPH1, and RN7SK as examples of Pol III transcripts (with RN7SK having a 5′ methylated triphosphate and therefore being resistant to CIP treatment; see main text); and ERCC190 and FLUC as examples of spiked-in in vitro transcripts with a defined triphosphorylated 5′ end. The Cq values are available in Supplemental Figure S1F. (C) Example of a Pol II TSS in the TMSB10 locus: The same positions (shaded in pink) are found in the CAGE data set. CIP treatment intensifies the signal, consistent with a Pol II TSS. (D) Example of Pol III TSS corresponding to the start of two vault RNAs (vtRNA1-1 and vtRNA1-2) located on Chr 5. The positions (shaded in pink) are missing in the CAGE data set. CIP treatment reduces the signal, consistent with non–Pol II TSS. In C and D, the tracks correspond to ReCappable-seq, CIP-ReCappable-seq, and CAGE read coverage (number of reads). All libraries were down-sampled to the same number of total mapped reads (63,300,000) to facilitate comparison. The four bottom tracks correspond to read density from public ENCODE DNase-seq from A549 cells (ENCFF473YHH, ENCFF809KIH, ENCFF821UUL, ENCFF961WXW).

    Techniques Used: Modification, Sequencing, Construct, Quantitative RT-PCR, Methylation, In Vitro

    3 desthiobiotin gtp dtb gtp  (New England Biolabs)


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    New England Biolabs 3 desthiobiotin gtp dtb gtp
    ReCappable-seq. (A) Principle of ReCappable-seq. (1) RNA is subjected to decapping with yDcpS, which acts on capped transcripts originating from Pol II transcription. Subsequently, the RNA is capped with a biotin-modified GTP analog <t>(3′-desthiobiotin-GTP)</t> using VCE. This biotinylation step allows enrichment of all primary transcripts on a streptavidin matrix. (2) Differentiation of Pol II from the non–Pol II transcripts is accomplished by sequencing a second library constructed with RNA treated with CIP before the yDcpS treatment, in order to remove the 5′ triphosphate from non–Pol II transcripts. (B) RT-qPCR assay measuring the recovery after streptavidin enrichment of various classes of transcripts such as RNA18S1 rRNA as an example of a processed transcript; ACTB, RPL19, MALAT1, FKBP5, TMSB10, H3C10, and HIST2H3B as examples of capped transcripts; RMRP, RPPH1, and RN7SK as examples of Pol III transcripts (with RN7SK having a 5′ methylated triphosphate and therefore being resistant to CIP treatment; see main text); and ERCC190 and FLUC as examples of spiked-in in vitro transcripts with a defined triphosphorylated 5′ end. The Cq values are available in Supplemental Figure S1F. (C) Example of a Pol II TSS in the TMSB10 locus: The same positions (shaded in pink) are found in the CAGE data set. CIP treatment intensifies the signal, consistent with a Pol II TSS. (D) Example of Pol III TSS corresponding to the start of two vault RNAs (vtRNA1-1 and vtRNA1-2) located on Chr 5. The positions (shaded in pink) are missing in the CAGE data set. CIP treatment reduces the signal, consistent with non–Pol II TSS. In C and D, the tracks correspond to ReCappable-seq, CIP-ReCappable-seq, and CAGE read coverage (number of reads). All libraries were down-sampled to the same number of total mapped reads (63,300,000) to facilitate comparison. The four bottom tracks correspond to read density from public ENCODE DNase-seq from A549 cells (ENCFF473YHH, ENCFF809KIH, ENCFF821UUL, ENCFF961WXW).
    3 Desthiobiotin Gtp Dtb Gtp, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Comprehensive determination of transcription start sites derived from all RNA polymerases using ReCappable-seq"

    Article Title: Comprehensive determination of transcription start sites derived from all RNA polymerases using ReCappable-seq

    Journal: Genome Research

    doi: 10.1101/gr.275784.121

    ReCappable-seq. (A) Principle of ReCappable-seq. (1) RNA is subjected to decapping with yDcpS, which acts on capped transcripts originating from Pol II transcription. Subsequently, the RNA is capped with a biotin-modified GTP analog (3′-desthiobiotin-GTP) using VCE. This biotinylation step allows enrichment of all primary transcripts on a streptavidin matrix. (2) Differentiation of Pol II from the non–Pol II transcripts is accomplished by sequencing a second library constructed with RNA treated with CIP before the yDcpS treatment, in order to remove the 5′ triphosphate from non–Pol II transcripts. (B) RT-qPCR assay measuring the recovery after streptavidin enrichment of various classes of transcripts such as RNA18S1 rRNA as an example of a processed transcript; ACTB, RPL19, MALAT1, FKBP5, TMSB10, H3C10, and HIST2H3B as examples of capped transcripts; RMRP, RPPH1, and RN7SK as examples of Pol III transcripts (with RN7SK having a 5′ methylated triphosphate and therefore being resistant to CIP treatment; see main text); and ERCC190 and FLUC as examples of spiked-in in vitro transcripts with a defined triphosphorylated 5′ end. The Cq values are available in Supplemental Figure S1F. (C) Example of a Pol II TSS in the TMSB10 locus: The same positions (shaded in pink) are found in the CAGE data set. CIP treatment intensifies the signal, consistent with a Pol II TSS. (D) Example of Pol III TSS corresponding to the start of two vault RNAs (vtRNA1-1 and vtRNA1-2) located on Chr 5. The positions (shaded in pink) are missing in the CAGE data set. CIP treatment reduces the signal, consistent with non–Pol II TSS. In C and D, the tracks correspond to ReCappable-seq, CIP-ReCappable-seq, and CAGE read coverage (number of reads). All libraries were down-sampled to the same number of total mapped reads (63,300,000) to facilitate comparison. The four bottom tracks correspond to read density from public ENCODE DNase-seq from A549 cells (ENCFF473YHH, ENCFF809KIH, ENCFF821UUL, ENCFF961WXW).
    Figure Legend Snippet: ReCappable-seq. (A) Principle of ReCappable-seq. (1) RNA is subjected to decapping with yDcpS, which acts on capped transcripts originating from Pol II transcription. Subsequently, the RNA is capped with a biotin-modified GTP analog (3′-desthiobiotin-GTP) using VCE. This biotinylation step allows enrichment of all primary transcripts on a streptavidin matrix. (2) Differentiation of Pol II from the non–Pol II transcripts is accomplished by sequencing a second library constructed with RNA treated with CIP before the yDcpS treatment, in order to remove the 5′ triphosphate from non–Pol II transcripts. (B) RT-qPCR assay measuring the recovery after streptavidin enrichment of various classes of transcripts such as RNA18S1 rRNA as an example of a processed transcript; ACTB, RPL19, MALAT1, FKBP5, TMSB10, H3C10, and HIST2H3B as examples of capped transcripts; RMRP, RPPH1, and RN7SK as examples of Pol III transcripts (with RN7SK having a 5′ methylated triphosphate and therefore being resistant to CIP treatment; see main text); and ERCC190 and FLUC as examples of spiked-in in vitro transcripts with a defined triphosphorylated 5′ end. The Cq values are available in Supplemental Figure S1F. (C) Example of a Pol II TSS in the TMSB10 locus: The same positions (shaded in pink) are found in the CAGE data set. CIP treatment intensifies the signal, consistent with a Pol II TSS. (D) Example of Pol III TSS corresponding to the start of two vault RNAs (vtRNA1-1 and vtRNA1-2) located on Chr 5. The positions (shaded in pink) are missing in the CAGE data set. CIP treatment reduces the signal, consistent with non–Pol II TSS. In C and D, the tracks correspond to ReCappable-seq, CIP-ReCappable-seq, and CAGE read coverage (number of reads). All libraries were down-sampled to the same number of total mapped reads (63,300,000) to facilitate comparison. The four bottom tracks correspond to read density from public ENCODE DNase-seq from A549 cells (ENCFF473YHH, ENCFF809KIH, ENCFF821UUL, ENCFF961WXW).

    Techniques Used: Modification, Sequencing, Construct, Quantitative RT-PCR, Methylation, In Vitro

    desthiobiotin teg guanosine 5  (New England Biolabs)


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    New England Biolabs 3 desthiobiotin teg guanosine 5 triphosphate dtbgtp
    3 Desthiobiotin Teg Guanosine 5 Triphosphate Dtbgtp, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    New England Biolabs 3 desthiobiotin gtp dtb gtp
    ReCappable-seq. (A) Principle of ReCappable-seq. (1) RNA is subjected to decapping with yDcpS, which acts on capped transcripts originating from Pol II transcription. Subsequently, the RNA is capped with a biotin-modified GTP analog <t>(3′-desthiobiotin-GTP)</t> using VCE. This biotinylation step allows enrichment of all primary transcripts on a streptavidin matrix. (2) Differentiation of Pol II from the non–Pol II transcripts is accomplished by sequencing a second library constructed with RNA treated with CIP before the yDcpS treatment, in order to remove the 5′ triphosphate from non–Pol II transcripts. (B) RT-qPCR assay measuring the recovery after streptavidin enrichment of various classes of transcripts such as RNA18S1 rRNA as an example of a processed transcript; ACTB, RPL19, MALAT1, FKBP5, TMSB10, H3C10, and HIST2H3B as examples of capped transcripts; RMRP, RPPH1, and RN7SK as examples of Pol III transcripts (with RN7SK having a 5′ methylated triphosphate and therefore being resistant to CIP treatment; see main text); and ERCC190 and FLUC as examples of spiked-in in vitro transcripts with a defined triphosphorylated 5′ end. The Cq values are available in Supplemental Figure S1F. (C) Example of a Pol II TSS in the TMSB10 locus: The same positions (shaded in pink) are found in the CAGE data set. CIP treatment intensifies the signal, consistent with a Pol II TSS. (D) Example of Pol III TSS corresponding to the start of two vault RNAs (vtRNA1-1 and vtRNA1-2) located on Chr 5. The positions (shaded in pink) are missing in the CAGE data set. CIP treatment reduces the signal, consistent with non–Pol II TSS. In C and D, the tracks correspond to ReCappable-seq, CIP-ReCappable-seq, and CAGE read coverage (number of reads). All libraries were down-sampled to the same number of total mapped reads (63,300,000) to facilitate comparison. The four bottom tracks correspond to read density from public ENCODE DNase-seq from A549 cells (ENCFF473YHH, ENCFF809KIH, ENCFF821UUL, ENCFF961WXW).
    3 Desthiobiotin Gtp Dtb Gtp, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ReCappable-seq. (A) Principle of ReCappable-seq. (1) RNA is subjected to decapping with yDcpS, which acts on capped transcripts originating from Pol II transcription. Subsequently, the RNA is capped with a biotin-modified GTP analog <t>(3′-desthiobiotin-GTP)</t> using VCE. This biotinylation step allows enrichment of all primary transcripts on a streptavidin matrix. (2) Differentiation of Pol II from the non–Pol II transcripts is accomplished by sequencing a second library constructed with RNA treated with CIP before the yDcpS treatment, in order to remove the 5′ triphosphate from non–Pol II transcripts. (B) RT-qPCR assay measuring the recovery after streptavidin enrichment of various classes of transcripts such as RNA18S1 rRNA as an example of a processed transcript; ACTB, RPL19, MALAT1, FKBP5, TMSB10, H3C10, and HIST2H3B as examples of capped transcripts; RMRP, RPPH1, and RN7SK as examples of Pol III transcripts (with RN7SK having a 5′ methylated triphosphate and therefore being resistant to CIP treatment; see main text); and ERCC190 and FLUC as examples of spiked-in in vitro transcripts with a defined triphosphorylated 5′ end. The Cq values are available in Supplemental Figure S1F. (C) Example of a Pol II TSS in the TMSB10 locus: The same positions (shaded in pink) are found in the CAGE data set. CIP treatment intensifies the signal, consistent with a Pol II TSS. (D) Example of Pol III TSS corresponding to the start of two vault RNAs (vtRNA1-1 and vtRNA1-2) located on Chr 5. The positions (shaded in pink) are missing in the CAGE data set. CIP treatment reduces the signal, consistent with non–Pol II TSS. In C and D, the tracks correspond to ReCappable-seq, CIP-ReCappable-seq, and CAGE read coverage (number of reads). All libraries were down-sampled to the same number of total mapped reads (63,300,000) to facilitate comparison. The four bottom tracks correspond to read density from public ENCODE DNase-seq from A549 cells (ENCFF473YHH, ENCFF809KIH, ENCFF821UUL, ENCFF961WXW).
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    ReCappable-seq. (A) Principle of ReCappable-seq. (1) RNA is subjected to decapping with yDcpS, which acts on capped transcripts originating from Pol II transcription. Subsequently, the RNA is capped with a biotin-modified GTP analog <t>(3′-desthiobiotin-GTP)</t> using VCE. This biotinylation step allows enrichment of all primary transcripts on a streptavidin matrix. (2) Differentiation of Pol II from the non–Pol II transcripts is accomplished by sequencing a second library constructed with RNA treated with CIP before the yDcpS treatment, in order to remove the 5′ triphosphate from non–Pol II transcripts. (B) RT-qPCR assay measuring the recovery after streptavidin enrichment of various classes of transcripts such as RNA18S1 rRNA as an example of a processed transcript; ACTB, RPL19, MALAT1, FKBP5, TMSB10, H3C10, and HIST2H3B as examples of capped transcripts; RMRP, RPPH1, and RN7SK as examples of Pol III transcripts (with RN7SK having a 5′ methylated triphosphate and therefore being resistant to CIP treatment; see main text); and ERCC190 and FLUC as examples of spiked-in in vitro transcripts with a defined triphosphorylated 5′ end. The Cq values are available in Supplemental Figure S1F. (C) Example of a Pol II TSS in the TMSB10 locus: The same positions (shaded in pink) are found in the CAGE data set. CIP treatment intensifies the signal, consistent with a Pol II TSS. (D) Example of Pol III TSS corresponding to the start of two vault RNAs (vtRNA1-1 and vtRNA1-2) located on Chr 5. The positions (shaded in pink) are missing in the CAGE data set. CIP treatment reduces the signal, consistent with non–Pol II TSS. In C and D, the tracks correspond to ReCappable-seq, CIP-ReCappable-seq, and CAGE read coverage (number of reads). All libraries were down-sampled to the same number of total mapped reads (63,300,000) to facilitate comparison. The four bottom tracks correspond to read density from public ENCODE DNase-seq from A549 cells (ENCFF473YHH, ENCFF809KIH, ENCFF821UUL, ENCFF961WXW).
    3 Desthiobiotin Teg Gtp, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ReCappable-seq. (A) Principle of ReCappable-seq. (1) RNA is subjected to decapping with yDcpS, which acts on capped transcripts originating from Pol II transcription. Subsequently, the RNA is capped with a biotin-modified GTP analog (3′-desthiobiotin-GTP) using VCE. This biotinylation step allows enrichment of all primary transcripts on a streptavidin matrix. (2) Differentiation of Pol II from the non–Pol II transcripts is accomplished by sequencing a second library constructed with RNA treated with CIP before the yDcpS treatment, in order to remove the 5′ triphosphate from non–Pol II transcripts. (B) RT-qPCR assay measuring the recovery after streptavidin enrichment of various classes of transcripts such as RNA18S1 rRNA as an example of a processed transcript; ACTB, RPL19, MALAT1, FKBP5, TMSB10, H3C10, and HIST2H3B as examples of capped transcripts; RMRP, RPPH1, and RN7SK as examples of Pol III transcripts (with RN7SK having a 5′ methylated triphosphate and therefore being resistant to CIP treatment; see main text); and ERCC190 and FLUC as examples of spiked-in in vitro transcripts with a defined triphosphorylated 5′ end. The Cq values are available in Supplemental Figure S1F. (C) Example of a Pol II TSS in the TMSB10 locus: The same positions (shaded in pink) are found in the CAGE data set. CIP treatment intensifies the signal, consistent with a Pol II TSS. (D) Example of Pol III TSS corresponding to the start of two vault RNAs (vtRNA1-1 and vtRNA1-2) located on Chr 5. The positions (shaded in pink) are missing in the CAGE data set. CIP treatment reduces the signal, consistent with non–Pol II TSS. In C and D, the tracks correspond to ReCappable-seq, CIP-ReCappable-seq, and CAGE read coverage (number of reads). All libraries were down-sampled to the same number of total mapped reads (63,300,000) to facilitate comparison. The four bottom tracks correspond to read density from public ENCODE DNase-seq from A549 cells (ENCFF473YHH, ENCFF809KIH, ENCFF821UUL, ENCFF961WXW).

    Journal: Genome Research

    Article Title: Comprehensive determination of transcription start sites derived from all RNA polymerases using ReCappable-seq

    doi: 10.1101/gr.275784.121

    Figure Lengend Snippet: ReCappable-seq. (A) Principle of ReCappable-seq. (1) RNA is subjected to decapping with yDcpS, which acts on capped transcripts originating from Pol II transcription. Subsequently, the RNA is capped with a biotin-modified GTP analog (3′-desthiobiotin-GTP) using VCE. This biotinylation step allows enrichment of all primary transcripts on a streptavidin matrix. (2) Differentiation of Pol II from the non–Pol II transcripts is accomplished by sequencing a second library constructed with RNA treated with CIP before the yDcpS treatment, in order to remove the 5′ triphosphate from non–Pol II transcripts. (B) RT-qPCR assay measuring the recovery after streptavidin enrichment of various classes of transcripts such as RNA18S1 rRNA as an example of a processed transcript; ACTB, RPL19, MALAT1, FKBP5, TMSB10, H3C10, and HIST2H3B as examples of capped transcripts; RMRP, RPPH1, and RN7SK as examples of Pol III transcripts (with RN7SK having a 5′ methylated triphosphate and therefore being resistant to CIP treatment; see main text); and ERCC190 and FLUC as examples of spiked-in in vitro transcripts with a defined triphosphorylated 5′ end. The Cq values are available in Supplemental Figure S1F. (C) Example of a Pol II TSS in the TMSB10 locus: The same positions (shaded in pink) are found in the CAGE data set. CIP treatment intensifies the signal, consistent with a Pol II TSS. (D) Example of Pol III TSS corresponding to the start of two vault RNAs (vtRNA1-1 and vtRNA1-2) located on Chr 5. The positions (shaded in pink) are missing in the CAGE data set. CIP treatment reduces the signal, consistent with non–Pol II TSS. In C and D, the tracks correspond to ReCappable-seq, CIP-ReCappable-seq, and CAGE read coverage (number of reads). All libraries were down-sampled to the same number of total mapped reads (63,300,000) to facilitate comparison. The four bottom tracks correspond to read density from public ENCODE DNase-seq from A549 cells (ENCFF473YHH, ENCFF809KIH, ENCFF821UUL, ENCFF961WXW).

    Article Snippet: Capping with 3′ desthiobiotin GTP (DTB-GTP) was performed in 50 µL total volume with 5 µL VCE (NEB M02080) and 0.5 mM DTB-GTP (NEB N0761), in the absence of SAM for 40 min at 37°C.

    Techniques: Modification, Sequencing, Construct, Quantitative RT-PCR, Methylation, In Vitro