bio print gel documentation imaging system (VILBER GmbH)
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VILBER GmbH
bio print gel documentation imaging system
Bio Print Gel Documentation Imaging System, supplied by VILBER GmbH, used in various techniques. Bioz Stars score: 98/100, based on 279 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bio+print+gel+documentation+imaging+system/BIO+PRINT/10__3390_slash_jof12050299-75-42-47
Average 98 stars, based on 279 article reviews
Bio Print Gel Documentation Imaging System, supplied by VILBER GmbH, used in various techniques. Bioz Stars score: 98/100, based on 279 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bio+print+gel+documentation+imaging+system/BIO+PRINT/10__3390_slash_jof12050299-75-42-47
Average 98 stars, based on 279 article reviews
bio print gel documentation imaging system - by Bioz Stars,
2026-09
98/100 stars
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Polymerase Chain Reaction:Article Title: Monogeneans on exotic Indian freshwater fish. 8. Co-translocation of Cichlidogyrus tilapiae (Monogenea, Dactylogyridae) with pindani Chindongo socolofi (Cichliformes, Cichlidae): first report of this parasite genus in India within aquarium trade facilities. Article Snippet: .. The size of the PCR products (2 lL) was analysed by electrophoresis in 1.2% agarose gel prepared in 1 TAE buffer, prestained with 0.1 lL/mL 10,000 Sybr Safe in dimethyl sulfoxide (Invitrogen, Waltham, MA, USA), at 90 V for 30 min, and visualised and documented on a Article Title: Monogeneans on exotic Indian freshwater fish. 8. Co-translocation of Cichlidogyrus tilapiae (Monogenea, Dactylogyridae) with pindani Chindongo socolofi (Cichliformes, Cichlidae): first report of this parasite genus in India within aquarium trade facilities Article Snippet: .. The size of the PCR products (2 μL) was analysed by electrophoresis in 1.2% agarose gel prepared in 1× TAE buffer, prestained with 0.1 μL/mL 10,000× Sybr Safe in dimethyl sulfoxide (Invitrogen, Waltham, MA, USA), at 90 V for 30 min, and visualised and documented on a Article Title: Impact of DNA Extraction Strategies on Genomic and Bioinformatic Outcomes in Eight Selected Fungal Strains Article Snippet: PCR was conducted with an initial denaturation at 94 ◦C for 5 min followed by 35 cycles at 94 ◦C for 30 s, 58 ◦C (ITS1/ITS4) or 60 ◦C (NL1/NL2) for 30 s, and 72 ◦C for 30 s, with https://doi.org/10.3390/jof12050299 a final extension at 72 ◦C for 7 min, in a Thermal Cycler (MiniAmpTM, Applied Biosystems, Waltham, MA, USA). .. All PCR products (5 μL, undiluted) were migrated on a 2% agarose (cat#: EZEE-AG500, Cleaver Scientific, Rugby, UK) gel containing 2.5 μL/100 mL of Xpert Green DNA Stain (GS01.0001, GRISP Research Solutions, Porto, Portugal) and visualized using a UV transilluminator with a Electrophoresis:Article Title: Monogeneans on exotic Indian freshwater fish. 8. Co-translocation of Cichlidogyrus tilapiae (Monogenea, Dactylogyridae) with pindani Chindongo socolofi (Cichliformes, Cichlidae): first report of this parasite genus in India within aquarium trade facilities. Article Snippet: .. The size of the PCR products (2 lL) was analysed by electrophoresis in 1.2% agarose gel prepared in 1 TAE buffer, prestained with 0.1 lL/mL 10,000 Sybr Safe in dimethyl sulfoxide (Invitrogen, Waltham, MA, USA), at 90 V for 30 min, and visualised and documented on a Article Title: Monogeneans on exotic Indian freshwater fish. 8. Co-translocation of Cichlidogyrus tilapiae (Monogenea, Dactylogyridae) with pindani Chindongo socolofi (Cichliformes, Cichlidae): first report of this parasite genus in India within aquarium trade facilities Article Snippet: .. The size of the PCR products (2 μL) was analysed by electrophoresis in 1.2% agarose gel prepared in 1× TAE buffer, prestained with 0.1 μL/mL 10,000× Sybr Safe in dimethyl sulfoxide (Invitrogen, Waltham, MA, USA), at 90 V for 30 min, and visualised and documented on a Article Title: Impact of DNA Extraction Strategies on Genomic and Bioinformatic Outcomes in Eight Selected Fungal Strains Article Snippet: 2.5.1. gDNA Purity Using NanoDrop Spectrophotometer A clean and calibrated NanoDrop®-2000 instrument (Thermo Fisher Scientific, USA) was used to estimate DNA concentration (ng/μL) and sample purity based on the A260/A280 (≈1.8–2.0) and A260/A230 (≈2.0–2.2) absorption ratios. .. Each collected gDNA sample was tested using 1 μL after adjusting the appropriate blank (Elution Buffer specific to each kit, except for kit1, where autoclaved ultrapure H2O was used). https://doi.org/10.3390/jof12050299 2.5.2. gDNA Integrity Quality Estimation by Gel Electrophoresis The presence, quality and gDNA integrity were then assessed by electrophoresis on 2% agarose gel (LE Agarose Multi-Purpose Agarose, Cleaver Scientific) using 1× TBE (Tris Borate EDTA) (0.1 M Tris, 0.09 M boric acid, and 1 mM EDTA) running buffer for 1 h at 100 V in a gel electrophoresis system (ENDUROTM) with a PowerPacTM Basic Power Supply (BIO-RAD, Hercules, CA, USA) and then visualized under UV light, with a Agarose Gel Electrophoresis:Article Title: Monogeneans on exotic Indian freshwater fish. 8. Co-translocation of Cichlidogyrus tilapiae (Monogenea, Dactylogyridae) with pindani Chindongo socolofi (Cichliformes, Cichlidae): first report of this parasite genus in India within aquarium trade facilities. Article Snippet: .. The size of the PCR products (2 lL) was analysed by electrophoresis in 1.2% agarose gel prepared in 1 TAE buffer, prestained with 0.1 lL/mL 10,000 Sybr Safe in dimethyl sulfoxide (Invitrogen, Waltham, MA, USA), at 90 V for 30 min, and visualised and documented on a Article Title: Monogeneans on exotic Indian freshwater fish. 8. Co-translocation of Cichlidogyrus tilapiae (Monogenea, Dactylogyridae) with pindani Chindongo socolofi (Cichliformes, Cichlidae): first report of this parasite genus in India within aquarium trade facilities Article Snippet: .. The size of the PCR products (2 μL) was analysed by electrophoresis in 1.2% agarose gel prepared in 1× TAE buffer, prestained with 0.1 μL/mL 10,000× Sybr Safe in dimethyl sulfoxide (Invitrogen, Waltham, MA, USA), at 90 V for 30 min, and visualised and documented on a Article Title: Impact of DNA Extraction Strategies on Genomic and Bioinformatic Outcomes in Eight Selected Fungal Strains Article Snippet: 2.5.1. gDNA Purity Using NanoDrop Spectrophotometer A clean and calibrated NanoDrop®-2000 instrument (Thermo Fisher Scientific, USA) was used to estimate DNA concentration (ng/μL) and sample purity based on the A260/A280 (≈1.8–2.0) and A260/A230 (≈2.0–2.2) absorption ratios. .. Each collected gDNA sample was tested using 1 μL after adjusting the appropriate blank (Elution Buffer specific to each kit, except for kit1, where autoclaved ultrapure H2O was used). https://doi.org/10.3390/jof12050299 2.5.2. gDNA Integrity Quality Estimation by Gel Electrophoresis The presence, quality and gDNA integrity were then assessed by electrophoresis on 2% agarose gel (LE Agarose Multi-Purpose Agarose, Cleaver Scientific) using 1× TBE (Tris Borate EDTA) (0.1 M Tris, 0.09 M boric acid, and 1 mM EDTA) running buffer for 1 h at 100 V in a gel electrophoresis system (ENDUROTM) with a PowerPacTM Basic Power Supply (BIO-RAD, Hercules, CA, USA) and then visualized under UV light, with a Imaging:Article Title: Monogeneans on exotic Indian freshwater fish. 8. Co-translocation of Cichlidogyrus tilapiae (Monogenea, Dactylogyridae) with pindani Chindongo socolofi (Cichliformes, Cichlidae): first report of this parasite genus in India within aquarium trade facilities. Article Snippet: .. The size of the PCR products (2 lL) was analysed by electrophoresis in 1.2% agarose gel prepared in 1 TAE buffer, prestained with 0.1 lL/mL 10,000 Sybr Safe in dimethyl sulfoxide (Invitrogen, Waltham, MA, USA), at 90 V for 30 min, and visualised and documented on a Article Title: Monogeneans on exotic Indian freshwater fish. 8. Co-translocation of Cichlidogyrus tilapiae (Monogenea, Dactylogyridae) with pindani Chindongo socolofi (Cichliformes, Cichlidae): first report of this parasite genus in India within aquarium trade facilities Article Snippet: .. The size of the PCR products (2 μL) was analysed by electrophoresis in 1.2% agarose gel prepared in 1× TAE buffer, prestained with 0.1 μL/mL 10,000× Sybr Safe in dimethyl sulfoxide (Invitrogen, Waltham, MA, USA), at 90 V for 30 min, and visualised and documented on a Article Title: Impact of DNA Extraction Strategies on Genomic and Bioinformatic Outcomes in Eight Selected Fungal Strains Article Snippet: PCR was conducted with an initial denaturation at 94 ◦C for 5 min followed by 35 cycles at 94 ◦C for 30 s, 58 ◦C (ITS1/ITS4) or 60 ◦C (NL1/NL2) for 30 s, and 72 ◦C for 30 s, with https://doi.org/10.3390/jof12050299 a final extension at 72 ◦C for 7 min, in a Thermal Cycler (MiniAmpTM, Applied Biosystems, Waltham, MA, USA). .. All PCR products (5 μL, undiluted) were migrated on a 2% agarose (cat#: EZEE-AG500, Cleaver Scientific, Rugby, UK) gel containing 2.5 μL/100 mL of Xpert Green DNA Stain (GS01.0001, GRISP Research Solutions, Porto, Portugal) and visualized using a UV transilluminator with a Article Title: Impact of DNA Extraction Strategies on Genomic and Bioinformatic Outcomes in Eight Selected Fungal Strains Article Snippet: 2.5.1. gDNA Purity Using NanoDrop Spectrophotometer A clean and calibrated NanoDrop®-2000 instrument (Thermo Fisher Scientific, USA) was used to estimate DNA concentration (ng/μL) and sample purity based on the A260/A280 (≈1.8–2.0) and A260/A230 (≈2.0–2.2) absorption ratios. .. Each collected gDNA sample was tested using 1 μL after adjusting the appropriate blank (Elution Buffer specific to each kit, except for kit1, where autoclaved ultrapure H2O was used). https://doi.org/10.3390/jof12050299 2.5.2. gDNA Integrity Quality Estimation by Gel Electrophoresis The presence, quality and gDNA integrity were then assessed by electrophoresis on 2% agarose gel (LE Agarose Multi-Purpose Agarose, Cleaver Scientific) using 1× TBE (Tris Borate EDTA) (0.1 M Tris, 0.09 M boric acid, and 1 mM EDTA) running buffer for 1 h at 100 V in a gel electrophoresis system (ENDUROTM) with a PowerPacTM Basic Power Supply (BIO-RAD, Hercules, CA, USA) and then visualized under UV light, with a Staining:Article Title: Impact of DNA Extraction Strategies on Genomic and Bioinformatic Outcomes in Eight Selected Fungal Strains Article Snippet: PCR was conducted with an initial denaturation at 94 ◦C for 5 min followed by 35 cycles at 94 ◦C for 30 s, 58 ◦C (ITS1/ITS4) or 60 ◦C (NL1/NL2) for 30 s, and 72 ◦C for 30 s, with https://doi.org/10.3390/jof12050299 a final extension at 72 ◦C for 7 min, in a Thermal Cycler (MiniAmpTM, Applied Biosystems, Waltham, MA, USA). .. All PCR products (5 μL, undiluted) were migrated on a 2% agarose (cat#: EZEE-AG500, Cleaver Scientific, Rugby, UK) gel containing 2.5 μL/100 mL of Xpert Green DNA Stain (GS01.0001, GRISP Research Solutions, Porto, Portugal) and visualized using a UV transilluminator with a Nucleic Acid Electrophoresis:Article Title: Impact of DNA Extraction Strategies on Genomic and Bioinformatic Outcomes in Eight Selected Fungal Strains Article Snippet: 2.5.1. gDNA Purity Using NanoDrop Spectrophotometer A clean and calibrated NanoDrop®-2000 instrument (Thermo Fisher Scientific, USA) was used to estimate DNA concentration (ng/μL) and sample purity based on the A260/A280 (≈1.8–2.0) and A260/A230 (≈2.0–2.2) absorption ratios. .. Each collected gDNA sample was tested using 1 μL after adjusting the appropriate blank (Elution Buffer specific to each kit, except for kit1, where autoclaved ultrapure H2O was used). https://doi.org/10.3390/jof12050299 2.5.2. gDNA Integrity Quality Estimation by Gel Electrophoresis The presence, quality and gDNA integrity were then assessed by electrophoresis on 2% agarose gel (LE Agarose Multi-Purpose Agarose, Cleaver Scientific) using 1× TBE (Tris Borate EDTA) (0.1 M Tris, 0.09 M boric acid, and 1 mM EDTA) running buffer for 1 h at 100 V in a gel electrophoresis system (ENDUROTM) with a PowerPacTM Basic Power Supply (BIO-RAD, Hercules, CA, USA) and then visualized under UV light, with a |