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Promega go script reverse transcriptase kit
Go Script Reverse Transcriptase Kit, 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/product/go+script+reverse+transcriptase+kits/reverse+transcriptase+reaction+kit/pmc10664280-274-58-62
Average 90 stars, based on 1 article reviews
go script reverse transcriptase kit - by Bioz Stars, 2026-09
90/100 stars

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Related Articles

cDNA Synthesis:

Article Title: RRP15 deficiency induces ribosome stress to inhibit colorectal cancer proliferation and metastasis via LZTS2-mediated β-catenin suppression.
Article Snippet: Total RNA was isolated using the TRIzol reagent (Life Technologies Inc.) following manufacturer’s instructions. .. One microgram RNA was used for cDNA synthesis using a reverse transcriptase reaction kit (Promega, Wisconsin, USA). qPCR was performed on a Biorad CFX 96 Touch using SYBR Green (TIANGEN BIOTECH, Beijing, China) as a dsDNA-specific fluorescent dye. ..

Article Title: KIF18A is a novel target of JNK1/c-Jun signaling pathway involved in tumorigenesis
Article Snippet: RNA Isolation and Quantitative Real-time PCR Total RNAs were extracted from siRNAs or plasmids-transfected cells utilizing TRIZOL reagent (Invitrogen, USA). .. One microgram RNA was used for cDNA synthesis with the aid of a reverse transcriptase reaction kit (Promega, USA), and quantitative real-time PCR (qRT-PCR) was performed on an ABI Prism 7000 Sequence Detection System (Applied Biosystems, USA) using SYBR Green (Vazyme, Nanjing, China) as a dsDNA-speci c uorescent dye. ..

Reverse Transcription:

Article Title: RRP15 deficiency induces ribosome stress to inhibit colorectal cancer proliferation and metastasis via LZTS2-mediated β-catenin suppression.
Article Snippet: Total RNA was isolated using the TRIzol reagent (Life Technologies Inc.) following manufacturer’s instructions. .. One microgram RNA was used for cDNA synthesis using a reverse transcriptase reaction kit (Promega, Wisconsin, USA). qPCR was performed on a Biorad CFX 96 Touch using SYBR Green (TIANGEN BIOTECH, Beijing, China) as a dsDNA-specific fluorescent dye. ..

Article Title: HOXA13 serves as a biomarker to predict neoadjuvant therapy efficacy in advanced colorectal cancer patients.
Article Snippet: DDP (Solarbio, Beijing, China) and 5- FU (Merck Millipore) were dissolved in the corresponding medium at the indicated doses, and the cells were treated for the indicated time. .. Quantitative real-time PCR (qRT-PCR) RNA extraction and reverse transcription reactions were performed as described previously [15] using a Reverse Transcriptase Reaction kit (Promega, Madison, USA). qPCR was conducted on a Bio-Rad CFX 96 Touch System (Bio-Rad, Hercules, USA) using SYBR Green (Vazyme) as a fluorescent dye. ..

Article Title: Mycobacterium tuberculosis transcriptional regulator Rv1019 is upregulated in hypoxia, and negatively regulates Rv3230c-Rv3229c operon encoding enzymes in the oleic acid biosynthetic pathway.
Article Snippet: .. RNA was resuspended in nuclease-free water and treated with DNase I. Complementary DNA (cDNA) was prepared using Reverse Transcriptase Core kit (Promega Corporation, Madison, WI, USA) according to the manufacturer’s protocol. .. A qPCR was performed using SYBR Green kit (Takara Bio Inc., San Jose, CA, USA).

Article Title: KIF18A is a novel target of JNK1/c-Jun signaling pathway involved in tumorigenesis
Article Snippet: RNA Isolation and Quantitative Real-time PCR Total RNAs were extracted from siRNAs or plasmids-transfected cells utilizing TRIZOL reagent (Invitrogen, USA). .. One microgram RNA was used for cDNA synthesis with the aid of a reverse transcriptase reaction kit (Promega, USA), and quantitative real-time PCR (qRT-PCR) was performed on an ABI Prism 7000 Sequence Detection System (Applied Biosystems, USA) using SYBR Green (Vazyme, Nanjing, China) as a dsDNA-speci c uorescent dye. ..

Article Title: A Phosphate-Starvation Enhanced Purple Acid Phosphatase, GmPAP23 Mediates Intracellular Phosphorus Recycling and Yield in Soybean.
Article Snippet: Plant internal phosphorus (P) recycling is a complex process, which is vital for improving plant P use efficiency.. However, the mechanisms underlying phosphate (Pi) release from internal organic‐P form remains to be deciphered in crops.. Here, we functionally characterised a Pi‐starvation responsive purple acid phosphatase (PAP), GmPAP23 in soybean (Glycine max).

Article Title: Lipid exchange at ER–trans-Golgi contact sites governs polarized cargo sorting
Article Snippet: Cluster scattering was quantified by measuring object perimeters over time-lapse imaging by CellProfiler 4.1.3 image analyses software. .. To analyze the mRNA expression of selected genes, 0.2 × 10 6 A549 cells were seeded into 6 cm–diameter culture dishes and then EMT was induced with 5 ng/ml TGF-β for 72 h. Total RNA was purified using the RNeasy Plus Mini kit (Qiagen) and a total amount of 2 μg RNA was reverse transcribed with a GO Script Reverse Transcriptase kit (Promega) using random primers. .. Relative transcript levels were measured in a LightCycler 480 Instrument (Roche) using Takyion No Rox SYBR MasterMix (Eurogentec).

Article Title: Initiation of B-type starch granules in wheat endosperm requires the plastidial α-glucan phosphorylase PHS1.
Article Snippet: .. Isolation, cloning, and plasmid construction for PHS1 and BGC1 Total RNA was extracted from leaves of 2-wk-old wheat seedlings using RNeasy kit (Qiagen) with on-column DNase I digestion (Qiagen). cDNA was synthesized (using 2 μg RNA) 4104 | THE PLANT CELL 2023: 35; 4091–4110 Kamble et al. D ow nloaded from https://academ ic.oup.com /plcell/article/35/11/4091/7246009 by guest on 19 January 2024 using the Go Script Reverse Transcriptase Kit (Promega) following the manufacturer’s instruction. .. The full-length wheat PHS1 cDNA sequence was amplified using gene-specific primers listed in Supplemental Table S2 and inserted into Gateway entry vector, pENTR, using the pENTR/D-TOPO kit (Invitrogen).

Real-time Polymerase Chain Reaction:

Article Title: RRP15 deficiency induces ribosome stress to inhibit colorectal cancer proliferation and metastasis via LZTS2-mediated β-catenin suppression.
Article Snippet: Total RNA was isolated using the TRIzol reagent (Life Technologies Inc.) following manufacturer’s instructions. .. One microgram RNA was used for cDNA synthesis using a reverse transcriptase reaction kit (Promega, Wisconsin, USA). qPCR was performed on a Biorad CFX 96 Touch using SYBR Green (TIANGEN BIOTECH, Beijing, China) as a dsDNA-specific fluorescent dye. ..

Article Title: HOXA13 serves as a biomarker to predict neoadjuvant therapy efficacy in advanced colorectal cancer patients.
Article Snippet: DDP (Solarbio, Beijing, China) and 5- FU (Merck Millipore) were dissolved in the corresponding medium at the indicated doses, and the cells were treated for the indicated time. .. Quantitative real-time PCR (qRT-PCR) RNA extraction and reverse transcription reactions were performed as described previously [15] using a Reverse Transcriptase Reaction kit (Promega, Madison, USA). qPCR was conducted on a Bio-Rad CFX 96 Touch System (Bio-Rad, Hercules, USA) using SYBR Green (Vazyme) as a fluorescent dye. ..

Article Title: KIF18A is a novel target of JNK1/c-Jun signaling pathway involved in tumorigenesis
Article Snippet: RNA Isolation and Quantitative Real-time PCR Total RNAs were extracted from siRNAs or plasmids-transfected cells utilizing TRIZOL reagent (Invitrogen, USA). .. One microgram RNA was used for cDNA synthesis with the aid of a reverse transcriptase reaction kit (Promega, USA), and quantitative real-time PCR (qRT-PCR) was performed on an ABI Prism 7000 Sequence Detection System (Applied Biosystems, USA) using SYBR Green (Vazyme, Nanjing, China) as a dsDNA-speci c uorescent dye. ..

SYBR Green Assay:

Article Title: RRP15 deficiency induces ribosome stress to inhibit colorectal cancer proliferation and metastasis via LZTS2-mediated β-catenin suppression.
Article Snippet: Total RNA was isolated using the TRIzol reagent (Life Technologies Inc.) following manufacturer’s instructions. .. One microgram RNA was used for cDNA synthesis using a reverse transcriptase reaction kit (Promega, Wisconsin, USA). qPCR was performed on a Biorad CFX 96 Touch using SYBR Green (TIANGEN BIOTECH, Beijing, China) as a dsDNA-specific fluorescent dye. ..

Article Title: HOXA13 serves as a biomarker to predict neoadjuvant therapy efficacy in advanced colorectal cancer patients.
Article Snippet: DDP (Solarbio, Beijing, China) and 5- FU (Merck Millipore) were dissolved in the corresponding medium at the indicated doses, and the cells were treated for the indicated time. .. Quantitative real-time PCR (qRT-PCR) RNA extraction and reverse transcription reactions were performed as described previously [15] using a Reverse Transcriptase Reaction kit (Promega, Madison, USA). qPCR was conducted on a Bio-Rad CFX 96 Touch System (Bio-Rad, Hercules, USA) using SYBR Green (Vazyme) as a fluorescent dye. ..

Article Title: KIF18A is a novel target of JNK1/c-Jun signaling pathway involved in tumorigenesis
Article Snippet: RNA Isolation and Quantitative Real-time PCR Total RNAs were extracted from siRNAs or plasmids-transfected cells utilizing TRIZOL reagent (Invitrogen, USA). .. One microgram RNA was used for cDNA synthesis with the aid of a reverse transcriptase reaction kit (Promega, USA), and quantitative real-time PCR (qRT-PCR) was performed on an ABI Prism 7000 Sequence Detection System (Applied Biosystems, USA) using SYBR Green (Vazyme, Nanjing, China) as a dsDNA-speci c uorescent dye. ..

RNA Extraction:

Article Title: HOXA13 serves as a biomarker to predict neoadjuvant therapy efficacy in advanced colorectal cancer patients.
Article Snippet: DDP (Solarbio, Beijing, China) and 5- FU (Merck Millipore) were dissolved in the corresponding medium at the indicated doses, and the cells were treated for the indicated time. .. Quantitative real-time PCR (qRT-PCR) RNA extraction and reverse transcription reactions were performed as described previously [15] using a Reverse Transcriptase Reaction kit (Promega, Madison, USA). qPCR was conducted on a Bio-Rad CFX 96 Touch System (Bio-Rad, Hercules, USA) using SYBR Green (Vazyme) as a fluorescent dye. ..

Sequencing:

Article Title: KIF18A is a novel target of JNK1/c-Jun signaling pathway involved in tumorigenesis
Article Snippet: RNA Isolation and Quantitative Real-time PCR Total RNAs were extracted from siRNAs or plasmids-transfected cells utilizing TRIZOL reagent (Invitrogen, USA). .. One microgram RNA was used for cDNA synthesis with the aid of a reverse transcriptase reaction kit (Promega, USA), and quantitative real-time PCR (qRT-PCR) was performed on an ABI Prism 7000 Sequence Detection System (Applied Biosystems, USA) using SYBR Green (Vazyme, Nanjing, China) as a dsDNA-speci c uorescent dye. ..

Expressing:

Article Title: Lipid exchange at ER–trans-Golgi contact sites governs polarized cargo sorting
Article Snippet: Cluster scattering was quantified by measuring object perimeters over time-lapse imaging by CellProfiler 4.1.3 image analyses software. .. To analyze the mRNA expression of selected genes, 0.2 × 10 6 A549 cells were seeded into 6 cm–diameter culture dishes and then EMT was induced with 5 ng/ml TGF-β for 72 h. Total RNA was purified using the RNeasy Plus Mini kit (Qiagen) and a total amount of 2 μg RNA was reverse transcribed with a GO Script Reverse Transcriptase kit (Promega) using random primers. .. Relative transcript levels were measured in a LightCycler 480 Instrument (Roche) using Takyion No Rox SYBR MasterMix (Eurogentec).

Purification:

Article Title: Lipid exchange at ER–trans-Golgi contact sites governs polarized cargo sorting
Article Snippet: Cluster scattering was quantified by measuring object perimeters over time-lapse imaging by CellProfiler 4.1.3 image analyses software. .. To analyze the mRNA expression of selected genes, 0.2 × 10 6 A549 cells were seeded into 6 cm–diameter culture dishes and then EMT was induced with 5 ng/ml TGF-β for 72 h. Total RNA was purified using the RNeasy Plus Mini kit (Qiagen) and a total amount of 2 μg RNA was reverse transcribed with a GO Script Reverse Transcriptase kit (Promega) using random primers. .. Relative transcript levels were measured in a LightCycler 480 Instrument (Roche) using Takyion No Rox SYBR MasterMix (Eurogentec).

other:

Article Title: Lipid exchange at ER-trans-Golgi contact sites governs polarized cargo sorting.
Article Snippet: To analyze the mRNA expression of selected genes, 0.2 × 106 A549 cells were seeded into 6 cm–diameter culture dishes and then EMT was induced with 5 ng/ml TGF-β for 72 h. Total RNA was purified using the RNeasy Plus Mini kit (Qiagen) and a total amount of 2 μg RNA was reverse transcribed with a GO Script Kovács et al. Journal of Cell Biology 13 of 18 OSBP governs polarized cargo sorting https://doi.org/10.1083/jcb.202307051 D ow nloaded from http://rupress.org/jcb/article-pdf/223/1/e202307051/1921269/jcb_202307051.pdf by Egypt user on 22 M arch 2024 Reverse Transcriptase kit (Promega) using random primers.

Isolation:

Article Title: Initiation of B-type starch granules in wheat endosperm requires the plastidial α-glucan phosphorylase PHS1.
Article Snippet: .. Isolation, cloning, and plasmid construction for PHS1 and BGC1 Total RNA was extracted from leaves of 2-wk-old wheat seedlings using RNeasy kit (Qiagen) with on-column DNase I digestion (Qiagen). cDNA was synthesized (using 2 μg RNA) 4104 | THE PLANT CELL 2023: 35; 4091–4110 Kamble et al. D ow nloaded from https://academ ic.oup.com /plcell/article/35/11/4091/7246009 by guest on 19 January 2024 using the Go Script Reverse Transcriptase Kit (Promega) following the manufacturer’s instruction. .. The full-length wheat PHS1 cDNA sequence was amplified using gene-specific primers listed in Supplemental Table S2 and inserted into Gateway entry vector, pENTR, using the pENTR/D-TOPO kit (Invitrogen).

Cloning:

Article Title: Initiation of B-type starch granules in wheat endosperm requires the plastidial α-glucan phosphorylase PHS1.
Article Snippet: .. Isolation, cloning, and plasmid construction for PHS1 and BGC1 Total RNA was extracted from leaves of 2-wk-old wheat seedlings using RNeasy kit (Qiagen) with on-column DNase I digestion (Qiagen). cDNA was synthesized (using 2 μg RNA) 4104 | THE PLANT CELL 2023: 35; 4091–4110 Kamble et al. D ow nloaded from https://academ ic.oup.com /plcell/article/35/11/4091/7246009 by guest on 19 January 2024 using the Go Script Reverse Transcriptase Kit (Promega) following the manufacturer’s instruction. .. The full-length wheat PHS1 cDNA sequence was amplified using gene-specific primers listed in Supplemental Table S2 and inserted into Gateway entry vector, pENTR, using the pENTR/D-TOPO kit (Invitrogen).

Plasmid Preparation:

Article Title: Initiation of B-type starch granules in wheat endosperm requires the plastidial α-glucan phosphorylase PHS1.
Article Snippet: .. Isolation, cloning, and plasmid construction for PHS1 and BGC1 Total RNA was extracted from leaves of 2-wk-old wheat seedlings using RNeasy kit (Qiagen) with on-column DNase I digestion (Qiagen). cDNA was synthesized (using 2 μg RNA) 4104 | THE PLANT CELL 2023: 35; 4091–4110 Kamble et al. D ow nloaded from https://academ ic.oup.com /plcell/article/35/11/4091/7246009 by guest on 19 January 2024 using the Go Script Reverse Transcriptase Kit (Promega) following the manufacturer’s instruction. .. The full-length wheat PHS1 cDNA sequence was amplified using gene-specific primers listed in Supplemental Table S2 and inserted into Gateway entry vector, pENTR, using the pENTR/D-TOPO kit (Invitrogen).

Synthesized:

Article Title: Initiation of B-type starch granules in wheat endosperm requires the plastidial α-glucan phosphorylase PHS1.
Article Snippet: .. Isolation, cloning, and plasmid construction for PHS1 and BGC1 Total RNA was extracted from leaves of 2-wk-old wheat seedlings using RNeasy kit (Qiagen) with on-column DNase I digestion (Qiagen). cDNA was synthesized (using 2 μg RNA) 4104 | THE PLANT CELL 2023: 35; 4091–4110 Kamble et al. D ow nloaded from https://academ ic.oup.com /plcell/article/35/11/4091/7246009 by guest on 19 January 2024 using the Go Script Reverse Transcriptase Kit (Promega) following the manufacturer’s instruction. .. The full-length wheat PHS1 cDNA sequence was amplified using gene-specific primers listed in Supplemental Table S2 and inserted into Gateway entry vector, pENTR, using the pENTR/D-TOPO kit (Invitrogen).



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