Small Technologies
Watch all the Genome Generation 2020 talks co-hosted with Arima Genomics now. Learn how you can generate amazing reference genomes using long-read sequencing and HiC.
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The Nanobind UL Library Prep Kit is available for pre-order. Reads Up to 4 Mb in length! See Poster #30 at ONT NCM or the product page for full details!
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Have a Tough Animal to Sequence? The Nanobind Tissue Big DNA Kit is Here! Use Short Read Eliminator to Deplete Small DNA.
Big Advances
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Our Technologies
We use micro-, nano-, and single molecule technologies to streamline every step in the genomics workflow from sample preparation to assays and detection instruments.
Nanobind magnetic disks are covered with nanoscale wrinkles and folds that protect DNA from shearing to generate longer reads across a broader range of sample types than any other technology.
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Extract high molecular weight (HMW = 50 kb - 300+ kb) and ultra high molecular weight (UHMW = 50 kb - 1+ Mb) DNA using a rapid bind, wash, and elute protocol. Compatible with manual or fully automated processing.
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From simple samples such as cells, bacteria, and blood to challenging samples such as animal tissues, insects, fish, fungi, and plants, nearly all have been sequenced using Nanobind. Thoroughly validated on Oxford Nanopore, PacBio, and Bionano Genomics.
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Nanobind Big DNA Kits are available now in the Store.
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Generate ultra long, megabase reads on MinION, GridION, and PromethION.
Micro and Nanoscale Silica
Each non-porous Nanobind disk is covered with a high density of micro- and nanostructured silica that can bind vast amounts of DNA and protect it from shearing. A single disk is used per extraction and can be processed either manually or automated using standard robotic instruments.Rapid Bind, Wash, and Elute
HMW DNA extraction can be performed using a simple bind, wash, and elute protocol that is automation compatible.HMW DNA (50 - 300+kb)
Nanobind Big DNA Kits can be used to obtain HMW DNA (50 - 300+ kb) from nearly all sample types. All samples have been validated by long-read sequencing on PacBio and ONT.UHMW DNA (50 kb - 1+ Mb)
Nanobind's High Molecular Weight (HMW) process provides DNA from 50 kb - 300 kb while the Ultra High Molecular Weight (UHMW) process provides DNA from 50 kb - 5.7 Mb+.Ultra Long Reads on ONT (4+ Mb)
Nanobind UHMW DNA Extraction and Nanobind UL Library Prep were used to generate the longest sequencing read ever, a 4.1 Mb length read from human cells. Ultra long reads (1 - 2+ Mb) can also be generated from blood, bacteria, animal tissues and plants.Cells, Bacteria, and Blood
The Nanobind CBB Big DNA Kit can be used to extract HMW and UHMW DNA from cultured cells, cultured bacteria, and whole blood.Plants
The Nanobind CBB Big DNA Kit can be used to extract HMW and UHMW DNA from cultured cells, cultured bacteria, and whole blood.Tissues
The Nanbind Tissue Big DNA Kit can be used to extract HMW DNA from human, mouse, monkey, pig, fish, crab, snail, slug, bird, and select insect samples.ONT Sequencing
Nanobind Big DNA Kits generate consistent nanopore data across a variety of sample types including cells, blood, bacteria, plants, and tissues.PacBio Sequencing
Nanobind Big DNA Kits have been used to sequence a comprehensive variety of sample types on PacBio Sequel.Show More
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Enhance long-read sequencing read lengths by depleting short DNA.
Short Read Eliminator Kits use a simple, 1 hour, size selective precipitation method. Three versions are available for DNA of all quality from amplicons to high quality HMW DNA.
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Protocols available for Oxford Nanopore MinION / GridION / PromethION. Protocols coming soon for PacBio Sequel I/II.
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Short Read Eliminator Kits are available now in the Store.
3 Depletion Cutoffs
Choose your SRE kit based on the quality of your input DNA from fragmented DNA or PCR amplicons to high quality HMW DNA.SRE XS Kit - Up to 10 kb
Short DNA depletion begins at 10 kb and increases in effectiveness as the DNA gets shorter.SRE Kit - Up to 25 kb
Short DNA depletion begins at 25 kb and increases in effectiveness as the DNA gets shorter.SRE XL Kit - Up to 40 kb
Short DNA depletion begins at 40 kb and increases in effectiveness as the DNA gets shorter.Simple Precipitation Process
Process up to 20 samples in 1 hour with just a centrifuge.Enhance Read Lengths
The read length enhancement scales with more aggressive depletion of short DNA.SRE XL on Nanobind Extracted Blood DNA
SRE XL begins depleting short DNA at 40 kb, leading to a 14 kb enhancement in read length N50.SRE on Puregene Extracted Cell DNA
SRE is compatible with DNA extracted using any technology.Show More
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Use single molecule analysis to better characterize your samples before costly sequencing or critical studies.
PicoSep Single Molecule System
Each PicoSep system consists of a single molecule detection module (shown), electronics module, and flow control module. The entire system is USB-controlled by laptop.PicoSep Separation Capillary
Separation is performed by injecting a sample plug into a buffer-filled microcapillary and driving with pressure. Single molecule sensitivity enables analysis to be performed using only 5 pL of sample and <20 DNA molecules.PicoSep Single Molecule DNA Sizing
DNA molecules are individually detected (bottom) and counted to form chromatograms (top). Each vertical spike is a single DNA molecule. Larger molecules elute first.PicoSep RNA Integrity Analysis
Single molecule sensitivity enables detection of minute amounts of RNA degradation and more accurate quantification of RNA integrity by direct counting of degraded molecules.PicoSep High MW DNA Sizing
PicoSep can accurately size and quantify high molecular weight DNA (100 kb+) in <2 hours. No electrophoresis method offers this speed, sizing resolution, or quantification capability.PicoSep Single Molecule Conformation
Individual single molecule spikes can be analyzed to determine molecular information such as size, packing density, and conformation. This trace shows a large DNA molecule randomly folded at the leading front and stretched out at the rear.Show More
Our Mission
We don't offer discounts. We don't offer samples.
However, once you are a customer, we will bend over backwards to help you get the sequencing data you need.
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We extract thousands of samples a year and sequence hundreds of them. We'll support you from the pre-analytical steps through extraction, library prep, and sequencing. You'll get support directly from the scientists who develop the products and who've likely already tested a sample similar to yours.
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If you run into trouble, you can send us your DNA to QC or your samples to extract. If you need an extra buffer, we usually include it for free. No matter what help you need, just ask.
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Ultimately, we're a bunch of scientists looking to do cool science. We just happen to sell kits, too.
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Careers
We’re always looking for smart, dedicated, and creative people to join our team. As in any startup environment, candidates who are flexible enough to fill many roles can be expected to grow quickly within the company and play a large part in shaping its future. Today, you may be working at the lab bench while tomorrow, you may be writing a patent, and the day after, you may be meeting with customers.
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Research Associate
Contact Us
Circulomics is a biotechnology company located in Baltimore, MD. To date, Circulomics has received $11M in funding from NIH and Maryland TEDCO to develop innovative platforms for nucleic acid sample preparation, long-read sequencing, nucleic acid assays, and single molecule analysis that will drive the research and clinical translation of genomics technologies from sequencing to expression profiling and biomarker analysis.
Circulomics Inc
701 E Pratt St, Baltimore, MD 21202
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