size select beads Search Results


beyomagtm magnetic bead pcr dna purification kit  (Beyotime)
99
Beyotime beyomagtm magnetic bead pcr dna purification kit
Beyomagtm Magnetic Bead Pcr Dna Purification Kit, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/size+select+beads/BeyoMag+DNA+Size+Selection+Magnetic+Beads/pm41239426-130-12-19
Average 99 stars, based on 1 article reviews
beyomagtm magnetic bead pcr dna purification kit - by Bioz Stars, 2026-10
99/100 stars
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sodium chloride  (Chem Impex International)
95
Chem Impex International sodium chloride
Sodium Chloride, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/size+select+beads/Sodium+chloride/10__3390_slash_molecules30112371-160-26-29
Average 95 stars, based on 1 article reviews
sodium chloride - by Bioz Stars, 2026-10
95/100 stars
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pronex size selection beads  (Promega)
90
Promega pronex size selection beads
Pronex Size Selection Beads, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/size+select+beads/pronex+size+selection+beads/pmc11189511-189-10-9
Average 90 stars, based on 1 article reviews
pronex size selection beads - by Bioz Stars, 2026-10
90/100 stars
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custom bead purification protocol spri size selection protocol for >1.5-2 kb dna fragments  (Oxford Nanopore)
90
Oxford Nanopore custom bead purification protocol spri size selection protocol for >1.5-2 kb dna fragments
Each line plot represents the read size distribution from each mock community species estimated from <t>the</t> <t>Nanopore</t> metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community <t>DNA</t> Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.
Custom Bead Purification Protocol Spri Size Selection Protocol For >1.5 2 Kb Dna Fragments, supplied by Oxford Nanopore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/size+select+beads/custom+bead+purification+protocol+spri+size+selection+protocol+for++1+5+2+kb+dna+fragments/bio_rxiv__645903-82-17-20
Average 90 stars, based on 1 article reviews
custom bead purification protocol spri size selection protocol for >1.5-2 kb dna fragments - by Bioz Stars, 2026-10
90/100 stars
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bead-based size selection aline pcrcleantm dx magnetic beads  (Aline Biosciences)
90
Aline Biosciences bead-based size selection aline pcrcleantm dx magnetic beads
Each line plot represents the read size distribution from each mock community species estimated from <t>the</t> <t>Nanopore</t> metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community <t>DNA</t> Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.
Bead Based Size Selection Aline Pcrcleantm Dx Magnetic Beads, supplied by Aline Biosciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/size+select+beads/bead+based+size+selection+aline+pcrcleantm+dx+magnetic+beads/pmc06871532-219-2-11
Average 90 stars, based on 1 article reviews
bead-based size selection aline pcrcleantm dx magnetic beads - by Bioz Stars, 2026-10
90/100 stars
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dna sizeselector-i magnetic beads  (Aline Biosciences)
90
Aline Biosciences dna sizeselector-i magnetic beads
Each line plot represents the read size distribution from each mock community species estimated from <t>the</t> <t>Nanopore</t> metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community <t>DNA</t> Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.
Dna Sizeselector I Magnetic Beads, supplied by Aline Biosciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/size+select+beads/dna+sizeselector+i+bead+based+size+selection+system/pm34384542-362-8-10
Average 90 stars, based on 1 article reviews
dna sizeselector-i magnetic beads - by Bioz Stars, 2026-10
90/100 stars
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size-selective beads  (Promega)
90
Promega size-selective beads
Each line plot represents the read size distribution from each mock community species estimated from <t>the</t> <t>Nanopore</t> metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community <t>DNA</t> Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.
Size Selective Beads, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/size+select+beads/size+selective+beads/pmc09017118__mmc3-301-46-44
Average 90 stars, based on 1 article reviews
size-selective beads - by Bioz Stars, 2026-10
90/100 stars
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tianseq size selection dna beads  (tiangen biotech co)
90
tiangen biotech co tianseq size selection dna beads
Each line plot represents the read size distribution from each mock community species estimated from <t>the</t> <t>Nanopore</t> metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community <t>DNA</t> Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.
Tianseq Size Selection Dna Beads, supplied by tiangen biotech co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/size+select+beads/TIANSeq+Size+Selection+DNA+Beads/pm36477655-132-18-24
Average 90 stars, based on 1 article reviews
tianseq size selection dna beads - by Bioz Stars, 2026-10
90/100 stars
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magicpure size selection dna beads  (tiangen biotech co)
92
tiangen biotech co magicpure size selection dna beads
Each line plot represents the read size distribution from each mock community species estimated from <t>the</t> <t>Nanopore</t> metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community <t>DNA</t> Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.
Magicpure Size Selection Dna Beads, supplied by tiangen biotech co, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/size+select+beads/TIANSeq+Size+Selection+DNA+Beads/pm38151562-50-0-9
Average 92 stars, based on 1 article reviews
magicpure size selection dna beads - by Bioz Stars, 2026-10
92/100 stars
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magnetic bead-based pcr purification system pronex size-selective purification system  (Promega)
90
Promega magnetic bead-based pcr purification system pronex size-selective purification system
Each line plot represents the read size distribution from each mock community species estimated from <t>the</t> <t>Nanopore</t> metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community <t>DNA</t> Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.
Magnetic Bead Based Pcr Purification System Pronex Size Selective Purification System, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/size+select+beads/magnetic+bead+based+pcr+purification+system+pronex+size+selective+purification+system/pm34997243-520-9-14
Average 90 stars, based on 1 article reviews
magnetic bead-based pcr purification system pronex size-selective purification system - by Bioz Stars, 2026-10
90/100 stars
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Image Search Results


Each line plot represents the read size distribution from each mock community species estimated from the Nanopore metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community DNA Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.

Journal: bioRxiv

Article Title: Enabling high-accuracy long-read amplicon sequences using unique molecular identifiers with Nanopore or PacBio sequencing

doi: 10.1101/645903

Figure Lengend Snippet: Each line plot represents the read size distribution from each mock community species estimated from the Nanopore metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community DNA Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.

Article Snippet: The PCR product was purified using a custom bead purification protocol “SPRI size selection protocol for >1.5-2 kb DNA fragments” (Oxford Nanopore, England) based on: dx.doi.org/10.17504/protocols.io.idmca46.

Techniques: Generated, High Molecular Weight, Extraction, Sequencing

Read coverage profiles of the ZymoBIOMICS Microbial Community DNA Standard based on shotgun Nanopore sequencing data. Each grey point is the average coverage value of a 10 kbp region within the genome. Colored points represents the position of the individual intragenomic rRNA operons. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [product D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is our data generated from a ZymoBIOMICS Microbial Community DNA Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell.

Journal: bioRxiv

Article Title: Enabling high-accuracy long-read amplicon sequences using unique molecular identifiers with Nanopore or PacBio sequencing

doi: 10.1101/645903

Figure Lengend Snippet: Read coverage profiles of the ZymoBIOMICS Microbial Community DNA Standard based on shotgun Nanopore sequencing data. Each grey point is the average coverage value of a 10 kbp region within the genome. Colored points represents the position of the individual intragenomic rRNA operons. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [product D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is our data generated from a ZymoBIOMICS Microbial Community DNA Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell.

Article Snippet: The PCR product was purified using a custom bead purification protocol “SPRI size selection protocol for >1.5-2 kb DNA fragments” (Oxford Nanopore, England) based on: dx.doi.org/10.17504/protocols.io.idmca46.

Techniques: Nanopore Sequencing, Generated