kapa hypercapture reagent kit (Roche)
Roche manufactures this product 
99
Structured Review
Roche
kapa hypercapture reagent kit
Kapa Hypercapture Reagent Kit, supplied by Roche, used in various techniques. Bioz Stars score: 99/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/kapa+hypercapture+reagent+kit/KAPA+Quantification+Kit/pmc12813098-89-28-32
Average 99 stars, based on 5 article reviews
Kapa Hypercapture Reagent Kit, supplied by Roche, used in various techniques. Bioz Stars score: 99/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/kapa+hypercapture+reagent+kit/KAPA+Quantification+Kit/pmc12813098-89-28-32
Average 99 stars, based on 5 article reviews
kapa hypercapture reagent kit - by Bioz Stars,
2026-09
99/100 stars
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Control:Article Title: Beyond tumor mutation burden: tumor neoantigen burden as a superior prognostic biomarker in resected gastric cancer Article Snippet: .. After quality control and quantification by 4200 TapeStation system (Agilent Technologies) and Flex fluorometer (Invitrogen), a total of 500 ng library distributed between 280–350 bp was captured by Hybridization:Article Title: Nanoscale dynamics of enhancer–promoter interactions during exit from pluripotency Article Snippet: .. For the enrichment of fragments containing the viewpoints of interest, two subsequent hybridization reactions were performed using the Article Title: Nanoscale dynamics of enhancer–promoter interactions during exit from pluripotency Article Snippet: For the first hybridization reaction, 2 μg of each uniquely indexed library were combined in 1:1 mass ratio with 5 μl per library mouse Cot-1 DNA (Thermo Fisher Scientific, 18440016) and desiccated at 45°C in a vacuum centrifuge. .. The DNA pellet was then resuspended in 6.7 μl per library Universal Enhancing Oligonucleotides, 14 μl per library of Hybridization buffer, 6 μl per library Hybridization Component H and 4.5 μl per library diluted biotinylated oligonucleotides (2.9 nM per probe) and incubated at 95°C for 5 min and at 47°C for 72 h. Pulldown of the viewpoint-containing fragments was performed with 51 μl of M-270 streptavidin Dynabeads (Thermo Fisher Scientific, 65306) per library and using the Article Title: Nanoscale dynamics of enhancer-promoter interactions during exit from pluripotency. Article Snippet: .. For the enrichment of fragments containing the viewpoints of interest, two subsequent hybridization reactions were performed using the Article Title: Nanoscale dynamics of enhancer-promoter interactions during exit from pluripotency. Article Snippet: For the first hybridization reaction, 2 μg of each uniquely indexed library were combined in 1:1 mass ratio with 5 μl per library mouse Cot-1 DNA (Thermo Fisher Scientific, 18440016) and desiccated at 45 ◦C in a vacuum centrifuge. .. The DNA pellet was then resuspended in 6.7 μl per library Universal Enhancing Oligonucleotides, 14 μl per library of Hybridization buffer, 6 μl per library Hybridization Component H and 4.5 μl per library diluted biotinylated oligonucleotides (2.9 nM per probe) and incubated at 95 ◦C for 5 min and at 47 ◦C for 72 h. Pulldown of the viewpoint-containing fragments was performed with 51 μl of M-270 streptavidin Dynabeads (Thermo Fisher Scientific, 65306) per library and using the Incubation:Article Title: Nanoscale dynamics of enhancer–promoter interactions during exit from pluripotency Article Snippet: For the first hybridization reaction, 2 μg of each uniquely indexed library were combined in 1:1 mass ratio with 5 μl per library mouse Cot-1 DNA (Thermo Fisher Scientific, 18440016) and desiccated at 45°C in a vacuum centrifuge. .. The DNA pellet was then resuspended in 6.7 μl per library Universal Enhancing Oligonucleotides, 14 μl per library of Hybridization buffer, 6 μl per library Hybridization Component H and 4.5 μl per library diluted biotinylated oligonucleotides (2.9 nM per probe) and incubated at 95°C for 5 min and at 47°C for 72 h. Pulldown of the viewpoint-containing fragments was performed with 51 μl of M-270 streptavidin Dynabeads (Thermo Fisher Scientific, 65306) per library and using the Article Title: Nanoscale dynamics of enhancer-promoter interactions during exit from pluripotency. Article Snippet: For the first hybridization reaction, 2 μg of each uniquely indexed library were combined in 1:1 mass ratio with 5 μl per library mouse Cot-1 DNA (Thermo Fisher Scientific, 18440016) and desiccated at 45 ◦C in a vacuum centrifuge. .. The DNA pellet was then resuspended in 6.7 μl per library Universal Enhancing Oligonucleotides, 14 μl per library of Hybridization buffer, 6 μl per library Hybridization Component H and 4.5 μl per library diluted biotinylated oligonucleotides (2.9 nM per probe) and incubated at 95 ◦C for 5 min and at 47 ◦C for 72 h. Pulldown of the viewpoint-containing fragments was performed with 51 μl of M-270 streptavidin Dynabeads (Thermo Fisher Scientific, 65306) per library and using the |