基于硅胶微珠的胶回收试剂盒。硅胶珠吸附力强,大小一致沉降均匀,可避免长片段DNA 片段在离心过程中的断裂降解,特别适合长片段DNA(硅胶微珠悬浮液样本 回收片段大小:20bp-50kbp典型回收效率:50– 90%A260/A280: 1.70 – 1.90洗脱体积:20 - 50 μL制制备时间:60 min /6 个制备结合率 10μL悬浮硅胶珠可吸附6μg DNAThe silica-matrix based kit for gel extraction without columns • Batch binding procedure• High binding capacity even for very small fragments ≥ 20 bp• Large DNA fragments are neither sheared nor degraded Technology Silica-matrix technology Format Silica bead suspension Sample material Fragment size 20 bp–approx. 50 kbp Typical recovery 50–90% A260/A280 1.7–1.9 Elution volume 20–50 µL Preparation time 60 min/6 preps Binding capacity 6 µg/10 µL suspension Applications • Extraction of DNA from agarose gels• Support protocol for concentration and desalination of reaction mixtures • Typical downstream applications: cloning, sequencing, PCR, restriction analysis NucleoTrap® Suspension, buffers 10 preps for gel extraction - NucleoTrap suspension, buffers pack of 10
高分子量DNA的后继纯化浓缩。快速高效回收100 bp–50 kb DNA.不含裂解液。Post clean-up and concentration of large sized DNA• Effective post clean-up and concentration of large-sized DNA for successful downstream applications• High recovery rates up to 90 % for DNA fragments 100 bp–50 kbp• Concentrate your DNA sample easily and faster compared to microdialysis filtrations units• 15 min/10 preps – time-saving procedureTechnology: Silica-membrane technology Format: Mini spin columns Sample material: Fragment size: 100 bp–approx. 50 kbp Typical recovery: 80–90 % A260/A280: 1.8–1.9 Elution volume: 50–100 µL Preparation time: 15 min/10 preps Binding capacity: 50 µg Applications • Clean-up and concentration of pre-purified DNA (organic extractions)• Clean-up and concentration of DNA from enzymatic reactions• Not recommended for gel or PCR clean-up • Typical downstream applications: qPCR, enzymatic reactions, Southern blotting, STR amplification NucleoSpin® gDNA Clean-up Columns,Collection Tubes (2 mL), buffers 10 preps for clean-up of genomic DNA in aqueous solutions - NucleoSpin gDNA Clean-up Columns, Collection Tubes, buffers
高分子量DNA的后继纯化浓缩。快速高效回收100 bp–50 kb DNA.不含裂解液。Post clean-up and concentration of large sized DNA• Effective post clean-up and concentration of large-sized DNA for successful downstream applications• High recovery rates up to 90 % for DNA fragments 100 bp–50 kbp• Concentrate your DNA sample easily and faster compared to microdialysis filtrations units• 15 min/10 preps – time-saving procedureTechnology: Silica-membrane technology Format: Mini spin columns Sample material: Fragment size: 100 bp–approx. 50 kbp Typical recovery: 80–90 % A260/A280: 1.8–1.9 Elution volume: 50–100 µL Preparation time: 15 min/10 preps Binding capacity: 50 µg Applications • Clean-up and concentration of pre-purified DNA (organic extractions)• Clean-up and concentration of DNA from enzymatic reactions• Not recommended for gel or PCR clean-up • Typical downstream applications: qPCR, enzymatic reactions, Southern blotting, STR amplification NucleoSpin® gDNA Clean-up Columns,Collection Tubes (2 mL), buffers 50 preps for clean-up of genomic DNA in aqueous solutions - NucleoSpin gDNA Clean-up Columns, Collection Tubes, buffers
NucleoTrap® Suspension for 100 preps 硅胶珠吸附力强,大小一致沉降均匀,可避免长片段DNA 片段在离心过程中的断裂降解,特别适合长片段DNA(硅胶微珠悬浮液样本 回收片段大小:20bp-50kbp典型回收效率:50– 90%A260/A280: 1.70 – 1.90洗脱体积:20 - 50 μL制制备时间:60 min /6 个制备结合率 10μL悬浮硅胶珠可吸附6μg DNAThe silica-matrix based kit for gel extraction without columns • Batch binding procedure• High binding capacity even for very small fragments ≥ 20 bp• Large DNA fragments are neither sheared nor degraded Technology Silica-matrix technology Format Silica bead suspension Sample material Fragment size 20 bp–approx. 50 kbp Typical recovery 50–90% A260/A280 1.7–1.9 Elution volume 20–50 µL Preparation time 60 min/6 preps Binding capacity 6 µg/10 µL suspension Applications • Extraction of DNA from agarose gels• Support protocol for concentration and desalination of reaction mixtures • Typical downstream applications: cloning, sequencing, PCR, restriction analysis NucleoTrap Suspension for 100 preps for gel extraction pack of 1 mL
基于硅胶微珠的胶回收试剂盒。硅胶珠吸附力强,大小一致沉降均匀,可避免长片段DNA 片段在离心过程中的断裂降解,特别适合长片段DNA(硅胶微珠悬浮液样本 回收片段大小:20bp-50kbp典型回收效率:50– 90%A260/A280: 1.70 – 1.90洗脱体积:20 - 50 μL制制备时间:60 min /6 个制备结合率 10μL悬浮硅胶珠可吸附6μg DNAThe silica-matrix based kit for gel extraction without columns • Batch binding procedure• High binding capacity even for very small fragments ≥ 20 bp• Large DNA fragments are neither sheared nor degraded Technology Silica-matrix technology Format Silica bead suspension Sample material Fragment size 20 bp–approx. 50 kbp Typical recovery 50–90% A260/A280 1.7–1.9 Elution volume 20–50 µL Preparation time 60 min/6 preps Binding capacity 6 µg/10 µL suspension Applications • Extraction of DNA from agarose gels• Support protocol for concentration and desalination of reaction mixtures • Typical downstream applications: cloning, sequencing, PCR, restriction analysis NucleoTrap® Suspension, buffers 100 preps for gel extraction - NucleoTrap Suspension, buffers pack of 100
高分子量DNA的后继纯化浓缩。快速高效回收100 bp–50 kb DNA.不含裂解液。Post clean-up and concentration of large sized DNA• Effective post clean-up and concentration of large-sized DNA for successful downstream applications• High recovery rates up to 90 % for DNA fragments 100 bp–50 kbp• Concentrate your DNA sample easily and faster compared to microdialysis filtrations units• 15 min/10 preps – time-saving procedureTechnology: Silica-membrane technology Format: Mini spin columns Sample material: Fragment size: 100 bp–approx. 50 kbp Typical recovery: 80–90 % A260/A280: 1.8–1.9 Elution volume: 50–100 µL Preparation time: 15 min/10 preps Binding capacity: 50 µg Applications • Clean-up and concentration of pre-purified DNA (organic extractions)• Clean-up and concentration of DNA from enzymatic reactions• Not recommended for gel or PCR clean-up • Typical downstream applications: qPCR, enzymatic reactions, Southern blotting, STR amplification NucleoSpin® gDNA Clean-up Columns,Collection Tubes (2 mL), buffers 250 preps for clean-up of genomic DNA in aqueous solutions - NucleoSpin gDNA Clean-up Columns, Collection Tubes, buffers