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t7-scribe standard rna ivt kit (cellscript, c-as3107)  (Cellscript Inc)

 
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    Structured Review

    Cellscript Inc t7-scribe standard rna ivt kit (cellscript, c-as3107)
    T7 Scribe Standard Rna Ivt Kit (Cellscript, C As3107), supplied by Cellscript 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/product/t7-scribe+standard+rna+ivt+kit+(cellscript%2C+c-as3107)/t7+scribetm+standard+rna+ivt+kit+c+as3107/us12297484-949-68-73
    Average 90 stars, based on 1 article reviews
    t7-scribe standard rna ivt kit (cellscript, c-as3107) - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Hybridization:

    Article Title: Methods, compositions, and kits for preparing nucleic acid libraries
    Article Snippet: Materials Target polynucleotide, human gDNA (BIO-35025) DNA fragmenting enzyme, KAPA Frag Kit (Roche, 7962517001) Adaptor template oligos (ATO), 1-019, 1-020 (Table 1) TAQ DNA polymerase (NEB, M0273L) TAQ DNA polymerase buffer (NEB, M0273L) DNA Polymerase I, Large (Klenow) Fragment (NEB, M0210L, M0212L) dNTPs (NEB, N0447s) USER® Enzyme (NEB, M5505S) Agencourt AMPure XP (Beckman Coulter, A63881) T7-Scribe Standard RNA IVT kit (CELLSCRIPT, C-AS3107) Method Annealing of an Adaptor Template Oligo(s) to Deoxyribonucleic Acids As in example 3, except using ATO 1-019.

    Article Title: Human-rabbit Hybrid Translation System to Explore the Function of Modified Ribosomes
    Article Snippet: T7-Scribe Standard RNA IVT kit (CELLSCRIPT, catalog number: C-AS3107, stored at -20 °C) (accompanied with 10× T7-Scribe transcription buffer, 100 mM ATP, 100 mM CTP, 100 mM UTP, 100 mM DTT, 40 U/μL ScriptGuard RNase inhibitor, T7-Scribe enzyme solution, RNase-free water, and DNase I) 59.

    Article Title: A specific eIF4A paralog facilitates LARP1-mediated translation repression during mTORC1 inhibition
    Article Snippet: Two guide RNAs were transcribed from the template PCR fragments (5′- TAATACGACTCACTATAGG GTGGCTCCGCGGATTATAAC GTTTAAGAGCTAT GCTGGAAACAGCATAGCAAGTTTAAATAAGGCTAGTCCGTTATCAACTTGA AAAAGTGGCACCGAGTCGGTGCTTTTTTT-3′ and 5′- TAATACGACTCACTATAGG CCAGAGGGAATGGACCCCGA GTTTAAGAGCTA TGCTGGAAACAGCATAGCAAGTTTAAATAAGGCTAGTCCGTTATCAACTTG AAAAAGTGGCACCGAGTCGGTGCTTTTTTT-3′, where the underlined characters represent sequences complementary to the EIF4A2 gene locus) by a T7-Scribe Standard RNA IVT kit (Cellscript, C-AS3107).

    Article Title: Sequence grammar and dynamics of subcellular translation revealed by APEX-Ribo-Seq
    Article Snippet: After hybridization of complementary DNA to the T7 promoter sequence, RNAs were amplified by in vitro transcription using the T7-Scribe Standard RNA IVT Kit (CELLSCRIPT, C-AS3107). rRNA depletion was performed using Human Ribo-Seq riboPOOL (siTOOLs biotech, dp-K024-000042) and Mouse-Rat Ribo-Seq riboPOOL (siTOOLs biotech, dp-K024-000052).

    Article Title: Methods, compositions, and kits for preparing nucleic acid libraries
    Article Snippet: Materials Target polynucleotide, human gDNA (BIO-35025) DNA fragmenting enzyme, KAPA Frag Kit (Roche, 7962517001) Adaptor template oligos (ATO), 1-021 (Table 1) TAQ DNA polymerase (NEB, M0273L) TAQ DNA polymerase buffer (NEB, M0273L) DNA Polymerase I, Large (Klenow) Fragment (NEB, M0210L, M0212L) dNTPs (NEB, N0447s) Phusion® High-Fidelity DNA Polymerase (NEB, M0530S) Phusion buffer (NEB, M0530S) USER® Enzyme (NEB, M5505S) S1 Nuclease (ThermoFisher, EN0321) Agencourt AMPure XP (Beckman Coulter, A63881) T7-Scribe Standard RNA IVT kit (CELLSCRIPT, C-AS3107) Method Annealing of an Adaptor Template Oligo(s) to Deoxyribonucleic Acids As in example 3, except the ATO has in addition to a sequence designed to function as an RNA polymerase promoter contains a hairpin produced with two short regions of partial or complete complementarity separated by a random, specifically designed, or specifically chosen sequence, 1-021.

    Article Title: RS-1 enhances CRISPR/Cas9- and TALEN-mediated knock-in efficiency
    Article Snippet: TALEN, Cas9 and RAD51 mRNAs were transcribed in vitro , caped and polyadenylated using the T7 mScript Standard mRNA Production System (C-MSC100625, CELLSCRIPT, Madison, WI). sgRNA was in vitro transcribed using T7-Scribe Standard RNA IVT Kit (C-AS3107, CELLSCRIPT).

    Article Title: Host targeted inhibitors of dengue virus and other viruses
    Article Snippet: In vitro transcripts were synthesized from PstI linearized pDENrep-FH using T7-Scribe Standard RNA IVT kit (CellScript C-AS3107) and m7G(5′)ppp(5′)A RNA cap structure analog (New England Biolabs S1405L) following the manufacturers instructions.

    Sequencing:

    Article Title: Methods, compositions, and kits for preparing nucleic acid libraries
    Article Snippet: Materials Target polynucleotide, human gDNA (BIO-35025) DNA fragmenting enzyme, KAPA Frag Kit (Roche, 7962517001) Adaptor template oligos (ATO), 1-019, 1-020 (Table 1) TAQ DNA polymerase (NEB, M0273L) TAQ DNA polymerase buffer (NEB, M0273L) DNA Polymerase I, Large (Klenow) Fragment (NEB, M0210L, M0212L) dNTPs (NEB, N0447s) USER® Enzyme (NEB, M5505S) Agencourt AMPure XP (Beckman Coulter, A63881) T7-Scribe Standard RNA IVT kit (CELLSCRIPT, C-AS3107) Method Annealing of an Adaptor Template Oligo(s) to Deoxyribonucleic Acids As in example 3, except using ATO 1-019.

    Article Title: Human-rabbit Hybrid Translation System to Explore the Function of Modified Ribosomes
    Article Snippet: T7-Scribe Standard RNA IVT kit (CELLSCRIPT, catalog number: C-AS3107, stored at -20 °C) (accompanied with 10× T7-Scribe transcription buffer, 100 mM ATP, 100 mM CTP, 100 mM UTP, 100 mM DTT, 40 U/μL ScriptGuard RNase inhibitor, T7-Scribe enzyme solution, RNase-free water, and DNase I) 59.

    Article Title: A specific eIF4A paralog facilitates LARP1-mediated translation repression during mTORC1 inhibition
    Article Snippet: Two guide RNAs were transcribed from the template PCR fragments (5′- TAATACGACTCACTATAGG GTGGCTCCGCGGATTATAAC GTTTAAGAGCTAT GCTGGAAACAGCATAGCAAGTTTAAATAAGGCTAGTCCGTTATCAACTTGA AAAAGTGGCACCGAGTCGGTGCTTTTTTT-3′ and 5′- TAATACGACTCACTATAGG CCAGAGGGAATGGACCCCGA GTTTAAGAGCTA TGCTGGAAACAGCATAGCAAGTTTAAATAAGGCTAGTCCGTTATCAACTTG AAAAAGTGGCACCGAGTCGGTGCTTTTTTT-3′, where the underlined characters represent sequences complementary to the EIF4A2 gene locus) by a T7-Scribe Standard RNA IVT kit (Cellscript, C-AS3107).

    Article Title: Sequence grammar and dynamics of subcellular translation revealed by APEX-Ribo-Seq
    Article Snippet: After hybridization of complementary DNA to the T7 promoter sequence, RNAs were amplified by in vitro transcription using the T7-Scribe Standard RNA IVT Kit (CELLSCRIPT, C-AS3107). rRNA depletion was performed using Human Ribo-Seq riboPOOL (siTOOLs biotech, dp-K024-000042) and Mouse-Rat Ribo-Seq riboPOOL (siTOOLs biotech, dp-K024-000052).

    Article Title: Methods, compositions, and kits for preparing nucleic acid libraries
    Article Snippet: Materials Target polynucleotide, human gDNA (BIO-35025) DNA fragmenting enzyme, KAPA Frag Kit (Roche, 7962517001) Adaptor template oligos (ATO), 1-021 (Table 1) TAQ DNA polymerase (NEB, M0273L) TAQ DNA polymerase buffer (NEB, M0273L) DNA Polymerase I, Large (Klenow) Fragment (NEB, M0210L, M0212L) dNTPs (NEB, N0447s) Phusion® High-Fidelity DNA Polymerase (NEB, M0530S) Phusion buffer (NEB, M0530S) USER® Enzyme (NEB, M5505S) S1 Nuclease (ThermoFisher, EN0321) Agencourt AMPure XP (Beckman Coulter, A63881) T7-Scribe Standard RNA IVT kit (CELLSCRIPT, C-AS3107) Method Annealing of an Adaptor Template Oligo(s) to Deoxyribonucleic Acids As in example 3, except the ATO has in addition to a sequence designed to function as an RNA polymerase promoter contains a hairpin produced with two short regions of partial or complete complementarity separated by a random, specifically designed, or specifically chosen sequence, 1-021.

    Article Title: RS-1 enhances CRISPR/Cas9- and TALEN-mediated knock-in efficiency
    Article Snippet: TALEN, Cas9 and RAD51 mRNAs were transcribed in vitro , caped and polyadenylated using the T7 mScript Standard mRNA Production System (C-MSC100625, CELLSCRIPT, Madison, WI). sgRNA was in vitro transcribed using T7-Scribe Standard RNA IVT Kit (C-AS3107, CELLSCRIPT).

    Article Title: Host targeted inhibitors of dengue virus and other viruses
    Article Snippet: In vitro transcripts were synthesized from PstI linearized pDENrep-FH using T7-Scribe Standard RNA IVT kit (CellScript C-AS3107) and m7G(5′)ppp(5′)A RNA cap structure analog (New England Biolabs S1405L) following the manufacturers instructions.

    Amplification:

    Article Title: Methods, compositions, and kits for preparing nucleic acid libraries
    Article Snippet: Materials Target polynucleotide, human gDNA (BIO-35025) DNA fragmenting enzyme, KAPA Frag Kit (Roche, 7962517001) Adaptor template oligos (ATO), 1-019, 1-020 (Table 1) TAQ DNA polymerase (NEB, M0273L) TAQ DNA polymerase buffer (NEB, M0273L) DNA Polymerase I, Large (Klenow) Fragment (NEB, M0210L, M0212L) dNTPs (NEB, N0447s) USER® Enzyme (NEB, M5505S) Agencourt AMPure XP (Beckman Coulter, A63881) T7-Scribe Standard RNA IVT kit (CELLSCRIPT, C-AS3107) Method Annealing of an Adaptor Template Oligo(s) to Deoxyribonucleic Acids As in example 3, except using ATO 1-019.

    Article Title: Human-rabbit Hybrid Translation System to Explore the Function of Modified Ribosomes
    Article Snippet: T7-Scribe Standard RNA IVT kit (CELLSCRIPT, catalog number: C-AS3107, stored at -20 °C) (accompanied with 10× T7-Scribe transcription buffer, 100 mM ATP, 100 mM CTP, 100 mM UTP, 100 mM DTT, 40 U/μL ScriptGuard RNase inhibitor, T7-Scribe enzyme solution, RNase-free water, and DNase I) 59.

    Article Title: A specific eIF4A paralog facilitates LARP1-mediated translation repression during mTORC1 inhibition
    Article Snippet: Two guide RNAs were transcribed from the template PCR fragments (5′- TAATACGACTCACTATAGG GTGGCTCCGCGGATTATAAC GTTTAAGAGCTAT GCTGGAAACAGCATAGCAAGTTTAAATAAGGCTAGTCCGTTATCAACTTGA AAAAGTGGCACCGAGTCGGTGCTTTTTTT-3′ and 5′- TAATACGACTCACTATAGG CCAGAGGGAATGGACCCCGA GTTTAAGAGCTA TGCTGGAAACAGCATAGCAAGTTTAAATAAGGCTAGTCCGTTATCAACTTG AAAAAGTGGCACCGAGTCGGTGCTTTTTTT-3′, where the underlined characters represent sequences complementary to the EIF4A2 gene locus) by a T7-Scribe Standard RNA IVT kit (Cellscript, C-AS3107).

    Article Title: Sequence grammar and dynamics of subcellular translation revealed by APEX-Ribo-Seq
    Article Snippet: After hybridization of complementary DNA to the T7 promoter sequence, RNAs were amplified by in vitro transcription using the T7-Scribe Standard RNA IVT Kit (CELLSCRIPT, C-AS3107). rRNA depletion was performed using Human Ribo-Seq riboPOOL (siTOOLs biotech, dp-K024-000042) and Mouse-Rat Ribo-Seq riboPOOL (siTOOLs biotech, dp-K024-000052).

    Article Title: Methods, compositions, and kits for preparing nucleic acid libraries
    Article Snippet: Materials Target polynucleotide, human gDNA (BIO-35025) DNA fragmenting enzyme, KAPA Frag Kit (Roche, 7962517001) Adaptor template oligos (ATO), 1-021 (Table 1) TAQ DNA polymerase (NEB, M0273L) TAQ DNA polymerase buffer (NEB, M0273L) DNA Polymerase I, Large (Klenow) Fragment (NEB, M0210L, M0212L) dNTPs (NEB, N0447s) Phusion® High-Fidelity DNA Polymerase (NEB, M0530S) Phusion buffer (NEB, M0530S) USER® Enzyme (NEB, M5505S) S1 Nuclease (ThermoFisher, EN0321) Agencourt AMPure XP (Beckman Coulter, A63881) T7-Scribe Standard RNA IVT kit (CELLSCRIPT, C-AS3107) Method Annealing of an Adaptor Template Oligo(s) to Deoxyribonucleic Acids As in example 3, except the ATO has in addition to a sequence designed to function as an RNA polymerase promoter contains a hairpin produced with two short regions of partial or complete complementarity separated by a random, specifically designed, or specifically chosen sequence, 1-021.

    Article Title: RS-1 enhances CRISPR/Cas9- and TALEN-mediated knock-in efficiency
    Article Snippet: TALEN, Cas9 and RAD51 mRNAs were transcribed in vitro , caped and polyadenylated using the T7 mScript Standard mRNA Production System (C-MSC100625, CELLSCRIPT, Madison, WI). sgRNA was in vitro transcribed using T7-Scribe Standard RNA IVT Kit (C-AS3107, CELLSCRIPT).

    Article Title: Host targeted inhibitors of dengue virus and other viruses
    Article Snippet: In vitro transcripts were synthesized from PstI linearized pDENrep-FH using T7-Scribe Standard RNA IVT kit (CellScript C-AS3107) and m7G(5′)ppp(5′)A RNA cap structure analog (New England Biolabs S1405L) following the manufacturers instructions.

    In Vitro:

    Article Title: Methods, compositions, and kits for preparing nucleic acid libraries
    Article Snippet: Materials Target polynucleotide, human gDNA (BIO-35025) DNA fragmenting enzyme, KAPA Frag Kit (Roche, 7962517001) Adaptor template oligos (ATO), 1-019, 1-020 (Table 1) TAQ DNA polymerase (NEB, M0273L) TAQ DNA polymerase buffer (NEB, M0273L) DNA Polymerase I, Large (Klenow) Fragment (NEB, M0210L, M0212L) dNTPs (NEB, N0447s) USER® Enzyme (NEB, M5505S) Agencourt AMPure XP (Beckman Coulter, A63881) T7-Scribe Standard RNA IVT kit (CELLSCRIPT, C-AS3107) Method Annealing of an Adaptor Template Oligo(s) to Deoxyribonucleic Acids As in example 3, except using ATO 1-019.

    Article Title: Human-rabbit Hybrid Translation System to Explore the Function of Modified Ribosomes
    Article Snippet: T7-Scribe Standard RNA IVT kit (CELLSCRIPT, catalog number: C-AS3107, stored at -20 °C) (accompanied with 10× T7-Scribe transcription buffer, 100 mM ATP, 100 mM CTP, 100 mM UTP, 100 mM DTT, 40 U/μL ScriptGuard RNase inhibitor, T7-Scribe enzyme solution, RNase-free water, and DNase I) 59.

    Article Title: A specific eIF4A paralog facilitates LARP1-mediated translation repression during mTORC1 inhibition
    Article Snippet: Two guide RNAs were transcribed from the template PCR fragments (5′- TAATACGACTCACTATAGG GTGGCTCCGCGGATTATAAC GTTTAAGAGCTAT GCTGGAAACAGCATAGCAAGTTTAAATAAGGCTAGTCCGTTATCAACTTGA AAAAGTGGCACCGAGTCGGTGCTTTTTTT-3′ and 5′- TAATACGACTCACTATAGG CCAGAGGGAATGGACCCCGA GTTTAAGAGCTA TGCTGGAAACAGCATAGCAAGTTTAAATAAGGCTAGTCCGTTATCAACTTG AAAAAGTGGCACCGAGTCGGTGCTTTTTTT-3′, where the underlined characters represent sequences complementary to the EIF4A2 gene locus) by a T7-Scribe Standard RNA IVT kit (Cellscript, C-AS3107).

    Article Title: Sequence grammar and dynamics of subcellular translation revealed by APEX-Ribo-Seq
    Article Snippet: After hybridization of complementary DNA to the T7 promoter sequence, RNAs were amplified by in vitro transcription using the T7-Scribe Standard RNA IVT Kit (CELLSCRIPT, C-AS3107). rRNA depletion was performed using Human Ribo-Seq riboPOOL (siTOOLs biotech, dp-K024-000042) and Mouse-Rat Ribo-Seq riboPOOL (siTOOLs biotech, dp-K024-000052).

    Article Title: Methods, compositions, and kits for preparing nucleic acid libraries
    Article Snippet: Materials Target polynucleotide, human gDNA (BIO-35025) DNA fragmenting enzyme, KAPA Frag Kit (Roche, 7962517001) Adaptor template oligos (ATO), 1-021 (Table 1) TAQ DNA polymerase (NEB, M0273L) TAQ DNA polymerase buffer (NEB, M0273L) DNA Polymerase I, Large (Klenow) Fragment (NEB, M0210L, M0212L) dNTPs (NEB, N0447s) Phusion® High-Fidelity DNA Polymerase (NEB, M0530S) Phusion buffer (NEB, M0530S) USER® Enzyme (NEB, M5505S) S1 Nuclease (ThermoFisher, EN0321) Agencourt AMPure XP (Beckman Coulter, A63881) T7-Scribe Standard RNA IVT kit (CELLSCRIPT, C-AS3107) Method Annealing of an Adaptor Template Oligo(s) to Deoxyribonucleic Acids As in example 3, except the ATO has in addition to a sequence designed to function as an RNA polymerase promoter contains a hairpin produced with two short regions of partial or complete complementarity separated by a random, specifically designed, or specifically chosen sequence, 1-021.

    Article Title: RS-1 enhances CRISPR/Cas9- and TALEN-mediated knock-in efficiency
    Article Snippet: TALEN, Cas9 and RAD51 mRNAs were transcribed in vitro , caped and polyadenylated using the T7 mScript Standard mRNA Production System (C-MSC100625, CELLSCRIPT, Madison, WI). sgRNA was in vitro transcribed using T7-Scribe Standard RNA IVT Kit (C-AS3107, CELLSCRIPT).

    Article Title: Host targeted inhibitors of dengue virus and other viruses
    Article Snippet: In vitro transcripts were synthesized from PstI linearized pDENrep-FH using T7-Scribe Standard RNA IVT kit (CellScript C-AS3107) and m7G(5′)ppp(5′)A RNA cap structure analog (New England Biolabs S1405L) following the manufacturers instructions.

    Produced:

    Article Title: Methods, compositions, and kits for preparing nucleic acid libraries
    Article Snippet: Materials Target polynucleotide, human gDNA (BIO-35025) DNA fragmenting enzyme, KAPA Frag Kit (Roche, 7962517001) Adaptor template oligos (ATO), 1-019, 1-020 (Table 1) TAQ DNA polymerase (NEB, M0273L) TAQ DNA polymerase buffer (NEB, M0273L) DNA Polymerase I, Large (Klenow) Fragment (NEB, M0210L, M0212L) dNTPs (NEB, N0447s) USER® Enzyme (NEB, M5505S) Agencourt AMPure XP (Beckman Coulter, A63881) T7-Scribe Standard RNA IVT kit (CELLSCRIPT, C-AS3107) Method Annealing of an Adaptor Template Oligo(s) to Deoxyribonucleic Acids As in example 3, except using ATO 1-019.

    Article Title: Human-rabbit Hybrid Translation System to Explore the Function of Modified Ribosomes
    Article Snippet: T7-Scribe Standard RNA IVT kit (CELLSCRIPT, catalog number: C-AS3107, stored at -20 °C) (accompanied with 10× T7-Scribe transcription buffer, 100 mM ATP, 100 mM CTP, 100 mM UTP, 100 mM DTT, 40 U/μL ScriptGuard RNase inhibitor, T7-Scribe enzyme solution, RNase-free water, and DNase I) 59.

    Article Title: A specific eIF4A paralog facilitates LARP1-mediated translation repression during mTORC1 inhibition
    Article Snippet: Two guide RNAs were transcribed from the template PCR fragments (5′- TAATACGACTCACTATAGG GTGGCTCCGCGGATTATAAC GTTTAAGAGCTAT GCTGGAAACAGCATAGCAAGTTTAAATAAGGCTAGTCCGTTATCAACTTGA AAAAGTGGCACCGAGTCGGTGCTTTTTTT-3′ and 5′- TAATACGACTCACTATAGG CCAGAGGGAATGGACCCCGA GTTTAAGAGCTA TGCTGGAAACAGCATAGCAAGTTTAAATAAGGCTAGTCCGTTATCAACTTG AAAAAGTGGCACCGAGTCGGTGCTTTTTTT-3′, where the underlined characters represent sequences complementary to the EIF4A2 gene locus) by a T7-Scribe Standard RNA IVT kit (Cellscript, C-AS3107).

    Article Title: Sequence grammar and dynamics of subcellular translation revealed by APEX-Ribo-Seq
    Article Snippet: After hybridization of complementary DNA to the T7 promoter sequence, RNAs were amplified by in vitro transcription using the T7-Scribe Standard RNA IVT Kit (CELLSCRIPT, C-AS3107). rRNA depletion was performed using Human Ribo-Seq riboPOOL (siTOOLs biotech, dp-K024-000042) and Mouse-Rat Ribo-Seq riboPOOL (siTOOLs biotech, dp-K024-000052).

    Article Title: Methods, compositions, and kits for preparing nucleic acid libraries
    Article Snippet: Materials Target polynucleotide, human gDNA (BIO-35025) DNA fragmenting enzyme, KAPA Frag Kit (Roche, 7962517001) Adaptor template oligos (ATO), 1-021 (Table 1) TAQ DNA polymerase (NEB, M0273L) TAQ DNA polymerase buffer (NEB, M0273L) DNA Polymerase I, Large (Klenow) Fragment (NEB, M0210L, M0212L) dNTPs (NEB, N0447s) Phusion® High-Fidelity DNA Polymerase (NEB, M0530S) Phusion buffer (NEB, M0530S) USER® Enzyme (NEB, M5505S) S1 Nuclease (ThermoFisher, EN0321) Agencourt AMPure XP (Beckman Coulter, A63881) T7-Scribe Standard RNA IVT kit (CELLSCRIPT, C-AS3107) Method Annealing of an Adaptor Template Oligo(s) to Deoxyribonucleic Acids As in example 3, except the ATO has in addition to a sequence designed to function as an RNA polymerase promoter contains a hairpin produced with two short regions of partial or complete complementarity separated by a random, specifically designed, or specifically chosen sequence, 1-021.

    Article Title: RS-1 enhances CRISPR/Cas9- and TALEN-mediated knock-in efficiency
    Article Snippet: TALEN, Cas9 and RAD51 mRNAs were transcribed in vitro , caped and polyadenylated using the T7 mScript Standard mRNA Production System (C-MSC100625, CELLSCRIPT, Madison, WI). sgRNA was in vitro transcribed using T7-Scribe Standard RNA IVT Kit (C-AS3107, CELLSCRIPT).

    Article Title: Host targeted inhibitors of dengue virus and other viruses
    Article Snippet: In vitro transcripts were synthesized from PstI linearized pDENrep-FH using T7-Scribe Standard RNA IVT kit (CellScript C-AS3107) and m7G(5′)ppp(5′)A RNA cap structure analog (New England Biolabs S1405L) following the manufacturers instructions.

    Derivative Assay:

    Article Title: Methods, compositions, and kits for preparing nucleic acid libraries
    Article Snippet: Materials Target polynucleotide, human gDNA (BIO-35025) DNA fragmenting enzyme, KAPA Frag Kit (Roche, 7962517001) Adaptor template oligos (ATO), 1-019, 1-020 (Table 1) TAQ DNA polymerase (NEB, M0273L) TAQ DNA polymerase buffer (NEB, M0273L) DNA Polymerase I, Large (Klenow) Fragment (NEB, M0210L, M0212L) dNTPs (NEB, N0447s) USER® Enzyme (NEB, M5505S) Agencourt AMPure XP (Beckman Coulter, A63881) T7-Scribe Standard RNA IVT kit (CELLSCRIPT, C-AS3107) Method Annealing of an Adaptor Template Oligo(s) to Deoxyribonucleic Acids As in example 3, except using ATO 1-019.

    Article Title: Human-rabbit Hybrid Translation System to Explore the Function of Modified Ribosomes
    Article Snippet: T7-Scribe Standard RNA IVT kit (CELLSCRIPT, catalog number: C-AS3107, stored at -20 °C) (accompanied with 10× T7-Scribe transcription buffer, 100 mM ATP, 100 mM CTP, 100 mM UTP, 100 mM DTT, 40 U/μL ScriptGuard RNase inhibitor, T7-Scribe enzyme solution, RNase-free water, and DNase I) 59.

    Article Title: A specific eIF4A paralog facilitates LARP1-mediated translation repression during mTORC1 inhibition
    Article Snippet: Two guide RNAs were transcribed from the template PCR fragments (5′- TAATACGACTCACTATAGG GTGGCTCCGCGGATTATAAC GTTTAAGAGCTAT GCTGGAAACAGCATAGCAAGTTTAAATAAGGCTAGTCCGTTATCAACTTGA AAAAGTGGCACCGAGTCGGTGCTTTTTTT-3′ and 5′- TAATACGACTCACTATAGG CCAGAGGGAATGGACCCCGA GTTTAAGAGCTA TGCTGGAAACAGCATAGCAAGTTTAAATAAGGCTAGTCCGTTATCAACTTG AAAAAGTGGCACCGAGTCGGTGCTTTTTTT-3′, where the underlined characters represent sequences complementary to the EIF4A2 gene locus) by a T7-Scribe Standard RNA IVT kit (Cellscript, C-AS3107).

    Article Title: Sequence grammar and dynamics of subcellular translation revealed by APEX-Ribo-Seq
    Article Snippet: After hybridization of complementary DNA to the T7 promoter sequence, RNAs were amplified by in vitro transcription using the T7-Scribe Standard RNA IVT Kit (CELLSCRIPT, C-AS3107). rRNA depletion was performed using Human Ribo-Seq riboPOOL (siTOOLs biotech, dp-K024-000042) and Mouse-Rat Ribo-Seq riboPOOL (siTOOLs biotech, dp-K024-000052).

    Article Title: Methods, compositions, and kits for preparing nucleic acid libraries
    Article Snippet: Materials Target polynucleotide, human gDNA (BIO-35025) DNA fragmenting enzyme, KAPA Frag Kit (Roche, 7962517001) Adaptor template oligos (ATO), 1-021 (Table 1) TAQ DNA polymerase (NEB, M0273L) TAQ DNA polymerase buffer (NEB, M0273L) DNA Polymerase I, Large (Klenow) Fragment (NEB, M0210L, M0212L) dNTPs (NEB, N0447s) Phusion® High-Fidelity DNA Polymerase (NEB, M0530S) Phusion buffer (NEB, M0530S) USER® Enzyme (NEB, M5505S) S1 Nuclease (ThermoFisher, EN0321) Agencourt AMPure XP (Beckman Coulter, A63881) T7-Scribe Standard RNA IVT kit (CELLSCRIPT, C-AS3107) Method Annealing of an Adaptor Template Oligo(s) to Deoxyribonucleic Acids As in example 3, except the ATO has in addition to a sequence designed to function as an RNA polymerase promoter contains a hairpin produced with two short regions of partial or complete complementarity separated by a random, specifically designed, or specifically chosen sequence, 1-021.

    Article Title: RS-1 enhances CRISPR/Cas9- and TALEN-mediated knock-in efficiency
    Article Snippet: TALEN, Cas9 and RAD51 mRNAs were transcribed in vitro , caped and polyadenylated using the T7 mScript Standard mRNA Production System (C-MSC100625, CELLSCRIPT, Madison, WI). sgRNA was in vitro transcribed using T7-Scribe Standard RNA IVT Kit (C-AS3107, CELLSCRIPT).

    Article Title: Host targeted inhibitors of dengue virus and other viruses
    Article Snippet: In vitro transcripts were synthesized from PstI linearized pDENrep-FH using T7-Scribe Standard RNA IVT kit (CellScript C-AS3107) and m7G(5′)ppp(5′)A RNA cap structure analog (New England Biolabs S1405L) following the manufacturers instructions.

    Polymerase Chain Reaction:

    Article Title: Methods, compositions, and kits for preparing nucleic acid libraries
    Article Snippet: Materials Target polynucleotide, human gDNA (BIO-35025) DNA fragmenting enzyme, KAPA Frag Kit (Roche, 7962517001) Adaptor template oligos (ATO), 1-019, 1-020 (Table 1) TAQ DNA polymerase (NEB, M0273L) TAQ DNA polymerase buffer (NEB, M0273L) DNA Polymerase I, Large (Klenow) Fragment (NEB, M0210L, M0212L) dNTPs (NEB, N0447s) USER® Enzyme (NEB, M5505S) Agencourt AMPure XP (Beckman Coulter, A63881) T7-Scribe Standard RNA IVT kit (CELLSCRIPT, C-AS3107) Method Annealing of an Adaptor Template Oligo(s) to Deoxyribonucleic Acids As in example 3, except using ATO 1-019.

    Article Title: Human-rabbit Hybrid Translation System to Explore the Function of Modified Ribosomes
    Article Snippet: T7-Scribe Standard RNA IVT kit (CELLSCRIPT, catalog number: C-AS3107, stored at -20 °C) (accompanied with 10× T7-Scribe transcription buffer, 100 mM ATP, 100 mM CTP, 100 mM UTP, 100 mM DTT, 40 U/μL ScriptGuard RNase inhibitor, T7-Scribe enzyme solution, RNase-free water, and DNase I) 59.

    Article Title: A specific eIF4A paralog facilitates LARP1-mediated translation repression during mTORC1 inhibition
    Article Snippet: Two guide RNAs were transcribed from the template PCR fragments (5′- TAATACGACTCACTATAGG GTGGCTCCGCGGATTATAAC GTTTAAGAGCTAT GCTGGAAACAGCATAGCAAGTTTAAATAAGGCTAGTCCGTTATCAACTTGA AAAAGTGGCACCGAGTCGGTGCTTTTTTT-3′ and 5′- TAATACGACTCACTATAGG CCAGAGGGAATGGACCCCGA GTTTAAGAGCTA TGCTGGAAACAGCATAGCAAGTTTAAATAAGGCTAGTCCGTTATCAACTTG AAAAAGTGGCACCGAGTCGGTGCTTTTTTT-3′, where the underlined characters represent sequences complementary to the EIF4A2 gene locus) by a T7-Scribe Standard RNA IVT kit (Cellscript, C-AS3107).

    Article Title: Sequence grammar and dynamics of subcellular translation revealed by APEX-Ribo-Seq
    Article Snippet: After hybridization of complementary DNA to the T7 promoter sequence, RNAs were amplified by in vitro transcription using the T7-Scribe Standard RNA IVT Kit (CELLSCRIPT, C-AS3107). rRNA depletion was performed using Human Ribo-Seq riboPOOL (siTOOLs biotech, dp-K024-000042) and Mouse-Rat Ribo-Seq riboPOOL (siTOOLs biotech, dp-K024-000052).

    Article Title: Methods, compositions, and kits for preparing nucleic acid libraries
    Article Snippet: Materials Target polynucleotide, human gDNA (BIO-35025) DNA fragmenting enzyme, KAPA Frag Kit (Roche, 7962517001) Adaptor template oligos (ATO), 1-021 (Table 1) TAQ DNA polymerase (NEB, M0273L) TAQ DNA polymerase buffer (NEB, M0273L) DNA Polymerase I, Large (Klenow) Fragment (NEB, M0210L, M0212L) dNTPs (NEB, N0447s) Phusion® High-Fidelity DNA Polymerase (NEB, M0530S) Phusion buffer (NEB, M0530S) USER® Enzyme (NEB, M5505S) S1 Nuclease (ThermoFisher, EN0321) Agencourt AMPure XP (Beckman Coulter, A63881) T7-Scribe Standard RNA IVT kit (CELLSCRIPT, C-AS3107) Method Annealing of an Adaptor Template Oligo(s) to Deoxyribonucleic Acids As in example 3, except the ATO has in addition to a sequence designed to function as an RNA polymerase promoter contains a hairpin produced with two short regions of partial or complete complementarity separated by a random, specifically designed, or specifically chosen sequence, 1-021.

    Article Title: RS-1 enhances CRISPR/Cas9- and TALEN-mediated knock-in efficiency
    Article Snippet: TALEN, Cas9 and RAD51 mRNAs were transcribed in vitro , caped and polyadenylated using the T7 mScript Standard mRNA Production System (C-MSC100625, CELLSCRIPT, Madison, WI). sgRNA was in vitro transcribed using T7-Scribe Standard RNA IVT Kit (C-AS3107, CELLSCRIPT).

    Article Title: Host targeted inhibitors of dengue virus and other viruses
    Article Snippet: In vitro transcripts were synthesized from PstI linearized pDENrep-FH using T7-Scribe Standard RNA IVT kit (CellScript C-AS3107) and m7G(5′)ppp(5′)A RNA cap structure analog (New England Biolabs S1405L) following the manufacturers instructions.

    Reporter Assay:

    Article Title: Methods, compositions, and kits for preparing nucleic acid libraries
    Article Snippet: Materials Target polynucleotide, human gDNA (BIO-35025) DNA fragmenting enzyme, KAPA Frag Kit (Roche, 7962517001) Adaptor template oligos (ATO), 1-019, 1-020 (Table 1) TAQ DNA polymerase (NEB, M0273L) TAQ DNA polymerase buffer (NEB, M0273L) DNA Polymerase I, Large (Klenow) Fragment (NEB, M0210L, M0212L) dNTPs (NEB, N0447s) USER® Enzyme (NEB, M5505S) Agencourt AMPure XP (Beckman Coulter, A63881) T7-Scribe Standard RNA IVT kit (CELLSCRIPT, C-AS3107) Method Annealing of an Adaptor Template Oligo(s) to Deoxyribonucleic Acids As in example 3, except using ATO 1-019.

    Article Title: Human-rabbit Hybrid Translation System to Explore the Function of Modified Ribosomes
    Article Snippet: T7-Scribe Standard RNA IVT kit (CELLSCRIPT, catalog number: C-AS3107, stored at -20 °C) (accompanied with 10× T7-Scribe transcription buffer, 100 mM ATP, 100 mM CTP, 100 mM UTP, 100 mM DTT, 40 U/μL ScriptGuard RNase inhibitor, T7-Scribe enzyme solution, RNase-free water, and DNase I) 59.

    Article Title: A specific eIF4A paralog facilitates LARP1-mediated translation repression during mTORC1 inhibition
    Article Snippet: Two guide RNAs were transcribed from the template PCR fragments (5′- TAATACGACTCACTATAGG GTGGCTCCGCGGATTATAAC GTTTAAGAGCTAT GCTGGAAACAGCATAGCAAGTTTAAATAAGGCTAGTCCGTTATCAACTTGA AAAAGTGGCACCGAGTCGGTGCTTTTTTT-3′ and 5′- TAATACGACTCACTATAGG CCAGAGGGAATGGACCCCGA GTTTAAGAGCTA TGCTGGAAACAGCATAGCAAGTTTAAATAAGGCTAGTCCGTTATCAACTTG AAAAAGTGGCACCGAGTCGGTGCTTTTTTT-3′, where the underlined characters represent sequences complementary to the EIF4A2 gene locus) by a T7-Scribe Standard RNA IVT kit (Cellscript, C-AS3107).

    Article Title: Sequence grammar and dynamics of subcellular translation revealed by APEX-Ribo-Seq
    Article Snippet: After hybridization of complementary DNA to the T7 promoter sequence, RNAs were amplified by in vitro transcription using the T7-Scribe Standard RNA IVT Kit (CELLSCRIPT, C-AS3107). rRNA depletion was performed using Human Ribo-Seq riboPOOL (siTOOLs biotech, dp-K024-000042) and Mouse-Rat Ribo-Seq riboPOOL (siTOOLs biotech, dp-K024-000052).

    Article Title: Methods, compositions, and kits for preparing nucleic acid libraries
    Article Snippet: Materials Target polynucleotide, human gDNA (BIO-35025) DNA fragmenting enzyme, KAPA Frag Kit (Roche, 7962517001) Adaptor template oligos (ATO), 1-021 (Table 1) TAQ DNA polymerase (NEB, M0273L) TAQ DNA polymerase buffer (NEB, M0273L) DNA Polymerase I, Large (Klenow) Fragment (NEB, M0210L, M0212L) dNTPs (NEB, N0447s) Phusion® High-Fidelity DNA Polymerase (NEB, M0530S) Phusion buffer (NEB, M0530S) USER® Enzyme (NEB, M5505S) S1 Nuclease (ThermoFisher, EN0321) Agencourt AMPure XP (Beckman Coulter, A63881) T7-Scribe Standard RNA IVT kit (CELLSCRIPT, C-AS3107) Method Annealing of an Adaptor Template Oligo(s) to Deoxyribonucleic Acids As in example 3, except the ATO has in addition to a sequence designed to function as an RNA polymerase promoter contains a hairpin produced with two short regions of partial or complete complementarity separated by a random, specifically designed, or specifically chosen sequence, 1-021.

    Article Title: RS-1 enhances CRISPR/Cas9- and TALEN-mediated knock-in efficiency
    Article Snippet: TALEN, Cas9 and RAD51 mRNAs were transcribed in vitro , caped and polyadenylated using the T7 mScript Standard mRNA Production System (C-MSC100625, CELLSCRIPT, Madison, WI). sgRNA was in vitro transcribed using T7-Scribe Standard RNA IVT Kit (C-AS3107, CELLSCRIPT).

    Article Title: Host targeted inhibitors of dengue virus and other viruses
    Article Snippet: In vitro transcripts were synthesized from PstI linearized pDENrep-FH using T7-Scribe Standard RNA IVT kit (CellScript C-AS3107) and m7G(5′)ppp(5′)A RNA cap structure analog (New England Biolabs S1405L) following the manufacturers instructions.

    Synthesized:

    Article Title: Methods, compositions, and kits for preparing nucleic acid libraries
    Article Snippet: Materials Target polynucleotide, human gDNA (BIO-35025) DNA fragmenting enzyme, KAPA Frag Kit (Roche, 7962517001) Adaptor template oligos (ATO), 1-019, 1-020 (Table 1) TAQ DNA polymerase (NEB, M0273L) TAQ DNA polymerase buffer (NEB, M0273L) DNA Polymerase I, Large (Klenow) Fragment (NEB, M0210L, M0212L) dNTPs (NEB, N0447s) USER® Enzyme (NEB, M5505S) Agencourt AMPure XP (Beckman Coulter, A63881) T7-Scribe Standard RNA IVT kit (CELLSCRIPT, C-AS3107) Method Annealing of an Adaptor Template Oligo(s) to Deoxyribonucleic Acids As in example 3, except using ATO 1-019.

    Article Title: Human-rabbit Hybrid Translation System to Explore the Function of Modified Ribosomes
    Article Snippet: T7-Scribe Standard RNA IVT kit (CELLSCRIPT, catalog number: C-AS3107, stored at -20 °C) (accompanied with 10× T7-Scribe transcription buffer, 100 mM ATP, 100 mM CTP, 100 mM UTP, 100 mM DTT, 40 U/μL ScriptGuard RNase inhibitor, T7-Scribe enzyme solution, RNase-free water, and DNase I) 59.

    Article Title: A specific eIF4A paralog facilitates LARP1-mediated translation repression during mTORC1 inhibition
    Article Snippet: Two guide RNAs were transcribed from the template PCR fragments (5′- TAATACGACTCACTATAGG GTGGCTCCGCGGATTATAAC GTTTAAGAGCTAT GCTGGAAACAGCATAGCAAGTTTAAATAAGGCTAGTCCGTTATCAACTTGA AAAAGTGGCACCGAGTCGGTGCTTTTTTT-3′ and 5′- TAATACGACTCACTATAGG CCAGAGGGAATGGACCCCGA GTTTAAGAGCTA TGCTGGAAACAGCATAGCAAGTTTAAATAAGGCTAGTCCGTTATCAACTTG AAAAAGTGGCACCGAGTCGGTGCTTTTTTT-3′, where the underlined characters represent sequences complementary to the EIF4A2 gene locus) by a T7-Scribe Standard RNA IVT kit (Cellscript, C-AS3107).

    Article Title: Sequence grammar and dynamics of subcellular translation revealed by APEX-Ribo-Seq
    Article Snippet: After hybridization of complementary DNA to the T7 promoter sequence, RNAs were amplified by in vitro transcription using the T7-Scribe Standard RNA IVT Kit (CELLSCRIPT, C-AS3107). rRNA depletion was performed using Human Ribo-Seq riboPOOL (siTOOLs biotech, dp-K024-000042) and Mouse-Rat Ribo-Seq riboPOOL (siTOOLs biotech, dp-K024-000052).

    Article Title: Methods, compositions, and kits for preparing nucleic acid libraries
    Article Snippet: Materials Target polynucleotide, human gDNA (BIO-35025) DNA fragmenting enzyme, KAPA Frag Kit (Roche, 7962517001) Adaptor template oligos (ATO), 1-021 (Table 1) TAQ DNA polymerase (NEB, M0273L) TAQ DNA polymerase buffer (NEB, M0273L) DNA Polymerase I, Large (Klenow) Fragment (NEB, M0210L, M0212L) dNTPs (NEB, N0447s) Phusion® High-Fidelity DNA Polymerase (NEB, M0530S) Phusion buffer (NEB, M0530S) USER® Enzyme (NEB, M5505S) S1 Nuclease (ThermoFisher, EN0321) Agencourt AMPure XP (Beckman Coulter, A63881) T7-Scribe Standard RNA IVT kit (CELLSCRIPT, C-AS3107) Method Annealing of an Adaptor Template Oligo(s) to Deoxyribonucleic Acids As in example 3, except the ATO has in addition to a sequence designed to function as an RNA polymerase promoter contains a hairpin produced with two short regions of partial or complete complementarity separated by a random, specifically designed, or specifically chosen sequence, 1-021.

    Article Title: RS-1 enhances CRISPR/Cas9- and TALEN-mediated knock-in efficiency
    Article Snippet: TALEN, Cas9 and RAD51 mRNAs were transcribed in vitro , caped and polyadenylated using the T7 mScript Standard mRNA Production System (C-MSC100625, CELLSCRIPT, Madison, WI). sgRNA was in vitro transcribed using T7-Scribe Standard RNA IVT Kit (C-AS3107, CELLSCRIPT).

    Article Title: Host targeted inhibitors of dengue virus and other viruses
    Article Snippet: In vitro transcripts were synthesized from PstI linearized pDENrep-FH using T7-Scribe Standard RNA IVT kit (CellScript C-AS3107) and m7G(5′)ppp(5′)A RNA cap structure analog (New England Biolabs S1405L) following the manufacturers instructions.



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