Elevate your PCR cleanup process with the CSR PCR purification kit, setting a new standard in efficiency and cost-effectiveness.
This kit delivers exceptional purification results, meeting or exceeding the performance of renowned market leaders. Say goodbye to tedious manual purification methods and embrace a streamlined workflow that saves you time and resources. Achieve unparalleled PCR product purity while maximizing your budget with CSR's PCR purification kit.
🍁 Researched, Developed and Manufactured in London, ON, Canada.
Features
Efficient PCR product purification
High-quality purification comparable to market leaders
Rapid and reliable removal of contaminants and inhibitors
User-friendly protocol for streamlined workflow
Outstanding cost-effectiveness without compromising quality
Applications
Purification of PCR amplicons
DNA sequencing cleanup
Genotyping and SNP analysis
Cloning and molecular cloning
Fragment analysis
Documentation
Protocol
SDS Sheets*
* Contact us for SDS sheets or COAs
Experience the gold standard in genomic DNA isolation and purification with the CSR Genomic DNA isolation and purification kit.
Designed to deliver exceptional purity and yield, this kit guarantees results that are on par with market leaders. Streamline your DNA extraction workflow and unlock the full potential of your samples without breaking the bank. With CSR's unparalleled cost savings to quality ratio, you can trust that your genomic DNA isolation needs are met with precision, reliability, and affordability.
🍁 Researched, Developed and Manufactured in London, ON, Canada.
Features
High-quality genomic DNA isolation and purification
Comparable purity and yield to market leaders
Efficient removal of contaminants and inhibitors
Streamlined protocol for fast and reliable results
Cost-effective solution without compromising quality
Applications
Genomic DNA extraction from cells or tissues
PCR amplification of target genes
Genotyping studies
Genetic screening and profiling
Next-generation sequencing (NGS) library preparation
Documentation
Protocol
SDS Sheets*
* Contact us for SDS sheets or COAs
CleanNGS magnetic bead cleanup kit
Fast, consistent DNA/RNA purification for sequencing workflows
CleanNGS is a magnetic bead-based cleanup system designed for NGS and Sanger sample and library prep. It supports both routine cleanup and size selection, helping you remove salts, primers, and small byproducts while keeping the fragments you actually want.
Why labs use it
High recovery, low carryover: clean eluates with minimal contaminants.Quick magnetic response: beads separate efficiently for shorter hands-on time.Stable, easy workflow: a simple, repeatable protocol that works manually or on a liquid handler.Cost-conscious alternative: built to drop into SPRI-style cleanup workflows without expensive consumables.
Reliable size selection, without the guessing game
Size selection with bead chemistry depends on the binding environment. CleanNGS includes pre-formulated solutions designed to deliver tight, reproducible selection for:
Left-side selection (remove small fragments)
Right-side selection (remove large fragments)
Double-sided selection (narrow fragment ranges)
That means fewer re-optimizations and more consistent libraries run-to-run.
One kit for DNA and RNA
CleanNGS is produced RNase-free, so the same kit can be used for DNA workflows and RNA applications where cleanliness matters.
Automation-ready
CleanNGS is well suited for high-throughput cleanup on common liquid handling platforms. It can be integrated into automated protocols to streamline repetitive NGS purification steps, while maintaining flexibility for day-to-day variation in sample types and volumes.
Documents:
User Manual
SDS
Brochure
Application Notes:
NGS Library Preparation
CleanNGS bead cleanup performs equal compared to the lllumina SPB or Ampure XP competitor kits
CleanNGS: Purification for Next Generation Sequencing Library Preparations
Customer Feedback:
“It looks to me like your CleanNGS beads work just as well as [competitor beads]. They are convenient as they are already prepared and can be ordered in smaller quantities.”Name and institution withheld upon request, 2023
“I plan to replace [competitor beads] with CleanNGS Beads for cleaning PCR products and NGS library.”Hung, UNL, 2023
“We have tested the [CleanNGS] beads and it worked great for us. I am going to place an order.”Yinan, MYU, 2022
The CSR Mammalian RNA Isolation Kit provides a rapid, robust method to purify high-quality total RNA from mammalian cell cultures and tissues using silica spin-column technology. In the presence of optimized chaotropic binding conditions, RNA binds to a silica membrane while contaminants are removed through sequential wash steps, producing RNA suitable for sensitive downstream workflows.
Each column supports a high binding capacity (up to 20 µg) for efficient recovery from a wide range of input amounts.
For applications that require minimal genomic DNA carryover, the kit can be used with an optional on-column DNase digestion using a dedicated DNase-on-column buffer, after which the DNase is removed during wash steps.
Purified RNA is eluted in DNase/Protease/RNase-free water (or low-salt RNase-free buffer), ready for immediate use or storage.
🍁 Researched, Developed and Manufactured in London, ON, Canada.
Features
High-purity total RNA isolation from mammalian cells and tissues
Silica spin columns with up to 20 µg binding capacity
Optional on-column DNase digestion to minimize genomic DNA contamination
Efficient removal of proteins, salts, and inhibitors via multi-step washing
Fast, streamlined workflow without phenol/chloroform extraction
Cost-effective performance without compromising yield or purity
Applications
Total RNA extraction from mammalian cell cultures
Total RNA extraction from mammalian tissues
RT-qPCR / RT-PCR and gene expression analysis
RNA-seq / NGS library preparation (after QC and DNase option as needed)
cDNA synthesis and downstream transcript profiling
General RNA workflows requiring low inhibitor carryover
Document
Protocol
SDS Sheets*
* Contact us for SDS sheets or COAs