Is anyone using SPRI beads other than Beckman Coulter's Agencourt AMPure XP? Is anyone using MagBio's HighPrep PCR beads?
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We just follow the DIY SPRI bead protocol here https://openwetware.org/wiki/SPRI_bead_mix. We tested our home-brewed mixture with Ampure beads and didn't find much difference.
It is extremely cheap to make compared to the Ampure beads. You could make a liter of it for 400 bucks.
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PCR Clean DX
These are from Aline Biosciences.
In my last lab our robotic company tried to tell me our preps weren't working because we used Aline. They sent us Ampure beads and we did a side-by-side comparison. Aline performed better and at about 1/3 the cost.
To sum up: YES! Use them! They are great and a good company to work with as well.
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SPRI Beads for DNA, RNA, microRNA & Oligo Purification
SPRI Beads (DNA & RNA Purification)
Optimized to purify DNA fragments of 100 bp and larger, and RNA fragments of 200 bases and larger.
Features:
Purification of DNA and RNA• DNA fragments > 100 bp Applications:
• RNA fragments > 200 nt• NGS Library preparation
• PCR fragment purification
• DNA and RNA fragment purification
• Other applications requiring purified DNA and RNA
SPRI Beads (microRNA & Oligo Purification)
Overcomes the hurdle of the short DNA/RNA recovery problem. DNA/RNA fragments shorter than 100 base pairs can be effectively recovered.
Features:
Purification of short DNA and RNA• microRNA
• dsDNA fragments >20 bp
• ssDNA fragments >20 nt
• RNA fragments >20 nt
• DNA/RNA hybrid fragments >20 nt
• Oligo and chimeric oligo >20 nt
Learn More
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SPRI Beads (DNA & RNA Purification)
Optimized to purify DNA fragments of 100 bp and larger, and RNA fragments of 200 bases and larger.
Features:
Purification of DNA and RNA• DNA fragments > 100 bp Applications:
• RNA fragments > 200 nt• NGS Library preparation
• PCR fragment purification
• DNA and RNA fragment purification
• Other applications requiring purified DNA and RNA
SPRI Beads (microRNA & Oligo Purification)
Overcomes the hurdle of the short DNA/RNA recovery problem. DNA/RNA fragments shorter than 100 base pairs can be effectively recovered.
Features:
Purification of short DNA and RNA• microRNA
• dsDNA fragments >20 bp
• ssDNA fragments >20 nt
• RNA fragments >20 nt
• DNA/RNA hybrid fragments >20 nt
• Oligo and chimeric oligo >20 nt
Learn More
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Hello everyone,
MagBio Genomics offers HighPrep PCR clean-up kit, a direct replacement to AMPure XP beads that is over 50% cheaper. No change to protocol is needed. Please reach out to me at [email protected] to inquire more.
Thank you.
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DINOMAG cleanup and size selection SPRI magenetic beads (cat# DN9004-75ML) works great as a direct replacement to AMPure XP at a much lower price! https://labscoop.com/us/en/product/r...magnetic-beads (probably ~50-80% less than other commercially available magnetic bead-based reagents listed)Last edited by carlw; 01-23-2024, 06:18 PM.
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Latest Articles
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by GATTACATLove this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
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Channel: Articles
07-01-2026, 11:43 AM -
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by SEQadmin2
I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.
Here are nine questions we think about, in roughly the order they matter, before...-
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