bio rad molecular imager gel doc xr (Bio-Rad)
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bio rad molecular imager gel doc xr
Bio Rad Molecular Imager Gel Doc Xr, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 5475 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/gel+doc+gel+imaging+system/Molecular+Imager+Gel+Doc+XR%2B+System/10__1093_slash_ijfood_slash_vvag100-80-7-7
Average 96 stars, based on 5475 article reviews
Bio Rad Molecular Imager Gel Doc Xr, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 5475 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/gel+doc+gel+imaging+system/Molecular+Imager+Gel+Doc+XR%2B+System/10__1093_slash_ijfood_slash_vvag100-80-7-7
Average 96 stars, based on 5475 article reviews
bio rad molecular imager gel doc xr - by Bioz Stars,
2026-09
96/100 stars
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Staining:Article Title: RNA-guided nucleases and active fragments and variants thereof and methods of use Article Snippet: Deep sequencing was performed on an Illumina Mi-Seq platform by a service provider (MOGene). .. Gels were stained with SYBR Gold DNA stain (Life Technologies) for 10 min and imaged with a Article Title: Crispr enzymes and systems Article Snippet: 200-500 ng total of the purified PCR products were mixed with 1 μl 10×Taq DNA Polymerase PCR buffer (Enzymatics) and ultrapure water to a final volume of 10 μl, and subjected to a re-annealing process to enable heteroduplex formation: 95° C. for 10 min, 95° C. to 85° C. ramping at −2° C./s, 85° C. to 25° C. at −0.25° C./s, and 25° C. hold for 1 min. After reannealing, products were treated with SURVEYOR nuclease and SURVEYOR enhancer S (Integrated DNA Technologies) following the manufacturer's recommended protocol, and analyzed on 4-20% Novex TBE polyacrylamide gels (Life Technologies). .. Gels were stained with SYBRTM Gold DNA stain (Life Technologies) for 10 min and imaged with a Article Title: Delivery and use of the CRISPR-CAS systems, vectors and compositions for hepatic targeting and therapy Article Snippet: Gels were stained with SYBR Gold DNA stain (Life Technologies) for 30 minutes and imaged with a Gel Doc gel imaging system (Bio-rad). .. Gels were stained with SYBR Gold DNA stain (Life Technologies) for 30 minutes and imaged with a Article Title: Crispr enzymes and systems Article Snippet: 200-500 ng total of the purified PCR products were mixed with 1 μl 10×Taq DNA Polymerase PCR buffer (Enzymatics) and ultrapure water to a final volume of 10 μl and subjected to a re-annealing process to enable heteroduplex formation: 95° C. for 10 min, 95° C. to 85° C. ramping at −2° C./s, 85° C. to 25° C. at −0.25° C./s, and 25° C. hold for 1 min. After reannealing, products were treated with SURVEYOR nuclease and SURVEYOR enhancer S (Integrated DNA Technologies) following the manufacturer's recommended protocol, and analyzed on 4-20% Novex TBE polyacrylamide gels (Life Technologies). .. Gels were stained with SYBR Gold DNA stain (Life Technologies) for 10 min and imaged with a Article Title: CRISPR enzymes and systems Article Snippet: 200-500 ng total of the purified PCR products were mixed with 1μ|10×Taq DNA Polymerase PCR buffer (Enzymatics) and ultrapure water to a final volume of 10 ii I, and subjected to a re— annealing process to enable heteroduplex formation: 95° C. for 10 min, 95° C. to 85° C. ramping at −2° C./s, 85° C. to 25° C. at −0.25° C./s, and 25° C. hold for 1 min. After reannealing, products were treated with SURVEYOR nuclease and SURVEYOR enhancer S (Integrated DNA Technologies) following the manufacturer's recommended protocol, and analyzed on 4-20% Novex TBE polyacrylamide gels (Life Technologies). .. Gels were stained with SYBR Gold DNA stain (Life Technologies) for 10 min and imaged with a Article Title: Systems, methods and compositions for sequence manipulation with optimized functional CRISPR-Cas systems Article Snippet: After re-annealing, products were treated with SURVEYOR nuclease and SURVEYOR enhancer S (Transgenomics) following the manufacturer's recommended protocol, and analyzed on 4-20% Novex TBE poly-acrylamide gels (Life Technologies). .. Gels were stained with SYBR Gold DNA stain (Life Technologies) for 30 minutes and imaged with a Imaging:Article Title: RNA-guided nucleases and active fragments and variants thereof and methods of use Article Snippet: Deep sequencing was performed on an Illumina Mi-Seq platform by a service provider (MOGene). .. Gels were stained with SYBR Gold DNA stain (Life Technologies) for 10 min and imaged with a Article Title: Enhancing CRISPR/Cas gene editing through modulating cellular mechanical properties for cancer therapy Article Snippet: .. Gels were imaged with a Article Title: Crispr enzymes and systems Article Snippet: 200-500 ng total of the purified PCR products were mixed with 1 μl 10×Taq DNA Polymerase PCR buffer (Enzymatics) and ultrapure water to a final volume of 10 μl, and subjected to a re-annealing process to enable heteroduplex formation: 95° C. for 10 min, 95° C. to 85° C. ramping at −2° C./s, 85° C. to 25° C. at −0.25° C./s, and 25° C. hold for 1 min. After reannealing, products were treated with SURVEYOR nuclease and SURVEYOR enhancer S (Integrated DNA Technologies) following the manufacturer's recommended protocol, and analyzed on 4-20% Novex TBE polyacrylamide gels (Life Technologies). .. Gels were stained with SYBRTM Gold DNA stain (Life Technologies) for 10 min and imaged with a Article Title: Delivery and use of the CRISPR-CAS systems, vectors and compositions for hepatic targeting and therapy Article Snippet: Gels were stained with SYBR Gold DNA stain (Life Technologies) for 30 minutes and imaged with a Gel Doc gel imaging system (Bio-rad). .. Gels were stained with SYBR Gold DNA stain (Life Technologies) for 30 minutes and imaged with a Article Title: Crispr enzymes and systems Article Snippet: 200-500 ng total of the purified PCR products were mixed with 1 μl 10×Taq DNA Polymerase PCR buffer (Enzymatics) and ultrapure water to a final volume of 10 μl and subjected to a re-annealing process to enable heteroduplex formation: 95° C. for 10 min, 95° C. to 85° C. ramping at −2° C./s, 85° C. to 25° C. at −0.25° C./s, and 25° C. hold for 1 min. After reannealing, products were treated with SURVEYOR nuclease and SURVEYOR enhancer S (Integrated DNA Technologies) following the manufacturer's recommended protocol, and analyzed on 4-20% Novex TBE polyacrylamide gels (Life Technologies). .. Gels were stained with SYBR Gold DNA stain (Life Technologies) for 10 min and imaged with a Article Title: CRISPR enzymes and systems Article Snippet: 200-500 ng total of the purified PCR products were mixed with 1μ|10×Taq DNA Polymerase PCR buffer (Enzymatics) and ultrapure water to a final volume of 10 ii I, and subjected to a re— annealing process to enable heteroduplex formation: 95° C. for 10 min, 95° C. to 85° C. ramping at −2° C./s, 85° C. to 25° C. at −0.25° C./s, and 25° C. hold for 1 min. After reannealing, products were treated with SURVEYOR nuclease and SURVEYOR enhancer S (Integrated DNA Technologies) following the manufacturer's recommended protocol, and analyzed on 4-20% Novex TBE polyacrylamide gels (Life Technologies). .. Gels were stained with SYBR Gold DNA stain (Life Technologies) for 10 min and imaged with a Article Title: IGFBP5 is an ROR1 ligand promoting glioblastoma invasion via ROR1/HER2-CREB signaling axis Article Snippet: In brief, 200 ng of the purified PCR product was denatured and reannealed in 2 μL of NEB buffer 2 (10×) as following: 95 °C, 5 min; 95-85 °C, −2 °C/s; 85-25 °C, −0.1 °C/s; then held at 4 °C. .. Then 1 μL of T7EI (NEB, USA) was added to the annealed PCR products and incubated at 37 °C for 1 h. Products were finally analyzed on 2% agarose gels and imaged with a Article Title: Systems, methods and compositions for sequence manipulation with optimized functional CRISPR-Cas systems Article Snippet: After re-annealing, products were treated with SURVEYOR nuclease and SURVEYOR enhancer S (Transgenomics) following the manufacturer's recommended protocol, and analyzed on 4-20% Novex TBE poly-acrylamide gels (Life Technologies). .. Gels were stained with SYBR Gold DNA stain (Life Technologies) for 30 minutes and imaged with a Polymerase Chain Reaction:Article Title: IGFBP5 is an ROR1 ligand promoting glioblastoma invasion via ROR1/HER2-CREB signaling axis Article Snippet: In brief, 200 ng of the purified PCR product was denatured and reannealed in 2 μL of NEB buffer 2 (10×) as following: 95 °C, 5 min; 95-85 °C, −2 °C/s; 85-25 °C, −0.1 °C/s; then held at 4 °C. .. Then 1 μL of T7EI (NEB, USA) was added to the annealed PCR products and incubated at 37 °C for 1 h. Products were finally analyzed on 2% agarose gels and imaged with a Incubation:Article Title: IGFBP5 is an ROR1 ligand promoting glioblastoma invasion via ROR1/HER2-CREB signaling axis Article Snippet: In brief, 200 ng of the purified PCR product was denatured and reannealed in 2 μL of NEB buffer 2 (10×) as following: 95 °C, 5 min; 95-85 °C, −2 °C/s; 85-25 °C, −0.1 °C/s; then held at 4 °C. .. Then 1 μL of T7EI (NEB, USA) was added to the annealed PCR products and incubated at 37 °C for 1 h. Products were finally analyzed on 2% agarose gels and imaged with a |