Feature
1. Super-premixed Design for a Simpler and More Efficient Workflow
● Ready-to-use premixed hybrid reagent simplifies reaction setup to only three components, reducing manual pipetting errors;
● All components are stored at uniformly at 2 ~ 8°C, eliminating repeated freeze-thaw cycles and minimizing cumbersome preparation steps;
● Wash-free beads design further streamlines operation and shortens the regular hybrid capture workflow to as little as 145 min.
2. Enhanced Compatibility for More Flexible Automation
● Supports 0.5-12 μg pooled library input and flexible hybrid times from 0.25-16 hr, balancing sample throughput with cost efficiency;
● Compatible with mainstream NGS platforms such as NovaSeq and DNBSEQ, with different adapter options to support multi-platform deployment;
● Simplifies automated workflow configuration and script development, enabling rapid automation deployment while significantly reducing instrument implementation and method validation costs.
3. Broad Probe Compatibility for Comprehensive Applications● Conventional Probes: Deliver uniform and stable capture performance, supporting multiple variant analyses for routine targeted sequencing applications such as companion diagnostics and MRD monitoring;
● MSRE Probes: Enable simultaneous detection of DNA mutations and methylation, supporting dual-biomarker analysis for early cancer signal identification;
● Exhaustive Methylation Probes: Provide accurate quantification of methylation levels, supporting methylation biomarker discovery and validation as well as multi-cancer early screening product development.
Note: The hybrid capture of Conventional DNA Library is shown as an example. Regular refers to the μCaler Hybrid Capture Reagents v2, while HyperMix refers to the μCaler HyperMix Hybrid Capture Kit.
* Hybrid time is flexible from 0.25-16 hr. 1 hr is recommended for Conventional DNA Library and 2 hr for Methylated DNA Library.
** Set the appropriate elution temperature according to the library type for use: 60℃ for Conventional DNA Library and 61℃ for Methylated DNA Library.
Performance
Ultra-large Pooled Library Input Capacity
Fully Compatible with Mainstream Sequencing Platforms
Figure 2. Capture performance of two μCaler hybrid capture reagents across different sequencing platforms.Pre-libraries were prepared using the NadPrep DNA Library Preparation Module v2 coupled with either the NadPrep Universal Stubby Adapter (UDI) Module or the NadPrep Universal Adapter (MDI) Module (for MGI). 500 ng of each pre-library was performed to hybrid capture using the μCaler Hybrid Capture Reagents v2 (Regular) or the μCaler HyperMix Hybrid Capture Kit (for Illumina®/MGI) (HyperMix) with the M71. Sequencing was performed on the NovaSeq 6000 (PE150) and DNBSEQ-T7 (PE150) platforms. A. Mappability and On-target rate; B. Target covered; C. Fold 80 base penalty; D. Average sequencing depth after deduplication
Consistent Detection Across Multiple Variant Types
Figure 3. Consistency between observed variant allele frequencies (VAFs) and the expected VAFs in reference standards using two μCaler hybrid capture reagents. 500 ng of each pre-library was performed to hybrid capture using Regular or HyperMix with the μCaler Custom Panel. Variant analysis was conducted using VarDict.
Note: Samples were PancancerLight 800 gDNA Reference Standard (GeneWell, GW-OGTM800), with an initial input amount of 50 ng.
Accurate Detection for Reliable DNA Methylation Analysis
Figure 4. Capture performance of two μCaler hybrid capture reagents using simulated samples with varying methylation levels. Pre-libraries were prepared
from 50 ng simulated samples using the NadPrep Methyl Library Preparation Module v2 and NadPrep Methyl Stubby Adapter (UDI) Module v2 (with 10 nt index) after
bisulfite conversion. 500 ng of each pre-library was performed to hybrid capture using Regular or HyperMix (2-hr hybridization) with the μCaler EMS Panel v1.0. A. Average
coverage depth across all CpG sites. B. CpG methylation levels in target regions.
Note: The samples consist of 100% Methylated DNA (Zymo, D5014-2) as a positive control and 0% Methylated DNA (Zymo, D5014-1) as a negative control, mixed at different ratios to simulate methylation levels (0%, 10% and 50%).
μCaler HyperMix Hybrid Capture Kit (for Illumina®)
| Color of Tube Cap | Component |
Volume |
Volume |
|
|
μHybCap HyperMix (for Illumina®) | 890 μL |
3×1,770 µL |
|
|
μEnhancer | 1,300 μL | 8 mL |
|
|
Hyper Streptavidin Beads | 160 μL |
920 μL |
|
/ |
Wash Buffer A Pro | 5.8 mL |
2×17.5 mL |
|
/ |
Wash Buffer B | 2.9 mL |
20 mL |
μCaler HyperMix Hybrid Capture Kit (for MGI)
| Color of Tube Cap | Component |
Volume |
Volume |
|
|
μHybCap HyperMix (for MGI) | 890 μL |
3×1,770 µL |
|
|
Hyper Streptavidin Beads | 160 μL |
920 μL |
|
/ |
Wash Buffer A Pro | 5.8 mL |
2×17.5 mL |
|
/ |
Wash Buffer B | 2.9 mL |
20 mL |
For research use only. Not for use in diagnostic procedures.
| Product | Catalog# |
| μCaler HyperMix Hybrid Capture Kit (for Illumina®), 16 rxn | 1105302 |
| μCaler HyperMix Hybrid Capture Kit (for Illumina®), 96 rxn | 1105301 |
| μCaler HyperMix Hybrid Capture Kit (for MGI), 16 rxn | 1105402 |
| μCaler HyperMix Hybrid Capture Kit (for MGI), 96 rxn | 1105401 |
For research use only. Not for use in diagnostic procedures.
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