superscript iii reverse transcriptase (Bio-Rad)
Bio-Rad is a verified supplier 
Bio-Rad manufactures this product 
99
Structured Review
Bio-Rad
superscript iii reverse transcriptase
Superscript Iii Reverse Transcriptase, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 6819 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/superscript+reverse+transcriptase+kit/IScript+C+DNA+Synthesis+Kit/pmc12289656-68-20-24
Average 99 stars, based on 6819 article reviews
Superscript Iii Reverse Transcriptase, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 6819 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/superscript+reverse+transcriptase+kit/IScript+C+DNA+Synthesis+Kit/pmc12289656-68-20-24
Average 99 stars, based on 6819 article reviews
superscript iii reverse transcriptase - by Bioz Stars,
2026-09
99/100 stars
Images
Related Articles
Isolation:Article Title: Transcriptional regulation in pluripotent stem cells by methyl CpG-binding protein 2 (MeCP2) Article Snippet: The virus-containing supernatant was collected 48 h after transfection, filtered through 0.45 μm filters (Millipore, Bedford, MA, USA) and concentrated by ultracentrifugation. iPSCs were incubated in the virus supernatant supplemented with protamine sulfate for 24 h, and then the cells were replaced in fresh ES culturing medium added puromycin at a final concentration of 1 μg/ml. iPSC colonies resistant to puromycin were selected for 2 weeks, and were used to confirm the knock-down of MeCP2. .. Total RNA was isolated using an RNeasy kit (QIAGEN) followed by cDNA synthesis using Article Title: Transcriptional regulation in pluripotent stem cells by methyl CpG-binding protein 2 (MeCP2) Article Snippet: The virus-containing supernatant was collected 48 h after transfection, filtered through 0.45 μm filters (Millipore, Bedford, MA, USA) and concentrated by ultracentrifugation. iPSCs were incubated in the virus supernatant supplemented with protamine sulfate for 24 h, and then the cells were replaced in fresh ES culturing medium added puromycin at a final concentration of 1 μg/ml. iPSC colonies resistant to puromycin were selected for 2 weeks, and were used to confirm the knock-down of MeCP2. .. Real time quantitative PCR Total RNA was isolated using an RNeasy kit (QIAGEN) followed by cDNA synthesis using cDNA Synthesis:Article Title: Transcriptional regulation in pluripotent stem cells by methyl CpG-binding protein 2 (MeCP2) Article Snippet: The virus-containing supernatant was collected 48 h after transfection, filtered through 0.45 μm filters (Millipore, Bedford, MA, USA) and concentrated by ultracentrifugation. iPSCs were incubated in the virus supernatant supplemented with protamine sulfate for 24 h, and then the cells were replaced in fresh ES culturing medium added puromycin at a final concentration of 1 μg/ml. iPSC colonies resistant to puromycin were selected for 2 weeks, and were used to confirm the knock-down of MeCP2. .. Total RNA was isolated using an RNeasy kit (QIAGEN) followed by cDNA synthesis using Article Title: Transcriptional regulation in pluripotent stem cells by methyl CpG-binding protein 2 (MeCP2) Article Snippet: The virus-containing supernatant was collected 48 h after transfection, filtered through 0.45 μm filters (Millipore, Bedford, MA, USA) and concentrated by ultracentrifugation. iPSCs were incubated in the virus supernatant supplemented with protamine sulfate for 24 h, and then the cells were replaced in fresh ES culturing medium added puromycin at a final concentration of 1 μg/ml. iPSC colonies resistant to puromycin were selected for 2 weeks, and were used to confirm the knock-down of MeCP2. .. Real time quantitative PCR Total RNA was isolated using an RNeasy kit (QIAGEN) followed by cDNA synthesis using Reverse Transcription:Article Title: Transcriptional regulation in pluripotent stem cells by methyl CpG-binding protein 2 (MeCP2) Article Snippet: The virus-containing supernatant was collected 48 h after transfection, filtered through 0.45 μm filters (Millipore, Bedford, MA, USA) and concentrated by ultracentrifugation. iPSCs were incubated in the virus supernatant supplemented with protamine sulfate for 24 h, and then the cells were replaced in fresh ES culturing medium added puromycin at a final concentration of 1 μg/ml. iPSC colonies resistant to puromycin were selected for 2 weeks, and were used to confirm the knock-down of MeCP2. .. Total RNA was isolated using an RNeasy kit (QIAGEN) followed by cDNA synthesis using Article Title: Transcriptional regulation in pluripotent stem cells by methyl CpG-binding protein 2 (MeCP2) Article Snippet: The virus-containing supernatant was collected 48 h after transfection, filtered through 0.45 μm filters (Millipore, Bedford, MA, USA) and concentrated by ultracentrifugation. iPSCs were incubated in the virus supernatant supplemented with protamine sulfate for 24 h, and then the cells were replaced in fresh ES culturing medium added puromycin at a final concentration of 1 μg/ml. iPSC colonies resistant to puromycin were selected for 2 weeks, and were used to confirm the knock-down of MeCP2. .. Real time quantitative PCR Total RNA was isolated using an RNeasy kit (QIAGEN) followed by cDNA synthesis using Real-time Polymerase Chain Reaction:Article Title: Transcriptional regulation in pluripotent stem cells by methyl CpG-binding protein 2 (MeCP2) Article Snippet: The virus-containing supernatant was collected 48 h after transfection, filtered through 0.45 μm filters (Millipore, Bedford, MA, USA) and concentrated by ultracentrifugation. iPSCs were incubated in the virus supernatant supplemented with protamine sulfate for 24 h, and then the cells were replaced in fresh ES culturing medium added puromycin at a final concentration of 1 μg/ml. iPSC colonies resistant to puromycin were selected for 2 weeks, and were used to confirm the knock-down of MeCP2. .. Real time quantitative PCR Total RNA was isolated using an RNeasy kit (QIAGEN) followed by cDNA synthesis using |