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CLM Polymerase
Market-leading performance with minimized PCR bias

The most comprehensive whole exome panel that covers the target regions of all major WES panels in the market. With our proprietary technologies, we provide industry-leading performance and efficiency with complete BI solution.
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Hybridization-based target enrichment panel with our intrinsic probe design, rebalancing, and molecular barcode technologies to efficiently analyze not only hard-to-capture areas but also challenging samples, such as damaged DNA or RNA.
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End-to-end customized target enrichment panel with assay optimization, validation and even complete BI support. Over 1,000 custom panels developed world-wide. White-labeled customized product for business expansion also available.
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Revolutionary Bioinformatics solution providing fast and
accurate, client-specific analysis services.
Trust CAS with your BI analysis !

Celemics offers easy-to-use kit with all components needed from RNA fragmentation to double-stranded cDNA synthesis suitable for NGS.
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Celemics exclusive enzymes and buffers for enhanced hybridization to ensure improved coverage and uniformity.
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Proven market-leading purification and size selection efficiency supported by Celemics’ unique magnetic bead-based chemistry. Compatible with all Celemics’ panels as well as other NGS providers
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High-quality streptavidin bead that selectively isolates biotinylated ligands bound to hybridization probes; minimizing DNA loss during the target enrichment process.
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CeleNM™ Bead streamlines library quantification and normalization in Next-Generation Sequencing (NGS). Say goodbye to traditional QC processes, saving time and costs while ensuring robust results. Experience uniform sequencing data distribution and comparable on-target ratios with CeleNM™ Bead.
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Celemics’ highly optimized polymerase ensures market-leading amplification efficiency and accuracy with minimized PCR bias and error rate.
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Highly optimized library preparation kit to be used with all Celemics ready-to-use or customized panels. Experience the incomparable efficiency and performance for NGS library preparation
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The most comprehensive whole exome panel that covers the target regions of all major WES panels in the market. With our proprietary technologies, we provide industry-leading performance and efficiency with complete BI solution.
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Celemics’ comprehensive NGS panel for somatic cancer allows highly accurate and comprehensive analysis for identifying significant mutations and variants for solid tumors.

Celemics’ comprehensive NGS panel for somatic cancer allows highly accurate and comprehensive analysis for identifying significant mutations and variants for solid tumors.

Celemics has developed NGS ctDNA-based kits for colon, breast, and lung cancer assays. We have integrated our market-leading proprietary technologies and thoroughly validated and optimized as ready-to-use panels for clinical diagnostics.

Celemics offers end-to-end NGS-based detection and discovery solutions for Biopharma, CRO, and Drug discovery research fields.

In order to overcome the limitations of analyzing clinical diseases with conventional whole exome sequencing, Celemics introduces NGS-based clinical diagnostic solution for efficient detection of disease-causing variants for inherited diseases.

Celemics offers flexible choice of assessing extensive target regions associated with Pharmacogenomics for client-specific drug prescription and drug metabolism.

Celemics’ virus panels are designed to detect and identify disease-causing viruses. With our exclusive technologies, we provide efficient and accurate detection of targeted virus trains as well as procurement of credible data for whole viral genome sequencing.

To fulfill the expectations and growing needs for sequencing animals and plants, Celemics offers range of ready-to-use applicable to agrigenomics field as well as an option for developing customized NGS panel to specifically fit individual research purposes.

With Celemics’ proprietary technologies for assay development and optimization, we offer complete and robust NGS solutions for transcriptome, fusion, and isoform analyses for various sample types and conditions.

Celemics provides comprehensive solution for DNA methylation sequencing with proprietary probes specifically designed for methyl-seq, enabling accurate detection of methylation sites.

Complete solution with flexible panel design for characterization and differentiation of a myriad of microbial species.

Accurate and efficient analysis of IGH population that can detect MRD as low as 10-6 with optimized primers that can minimize sequencing loss and PCR duplications.

Celemics introduces revolutionary BI solution aiming to provide client-specific service. We provide fast, accurate, and sophisticated analyses of your NGS data accompanied by our proprietary bioinformatics pipeline.

The most comprehensive whole exome panel that covers the target regions of all major WES panels in the market. With our proprietary technologies, we provide industry-leading performance and efficiency with complete BI solution.
View Detail >
End-to-end customized target enrichment panel with assay optimization, validation and even complete BI support. Over 1,000 custom panels developed world-wide. White-labeled customized product for business expansion also available.
View Detail >
Utilizing NGS-based target enrichment methods for higher genotyping efficiency and accuracy. Providing cost-effective and optimized experiment compared to conventional methods, such as GBS, PCR and microarray in plant and animal research
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Revolutionary Bioinformatics solution providing fast and
accurate, client-specific analysis services.
Trust CAS with your BI analysis

Providing NGS-based diagnostics solutions for biopharma companies. Celemics can develop and deliver a flexible customization and commercialization services while maintaining the market-leading performance for our clients interested in clinical and companion diagnostics.
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Tailored-fit customized assay development from designing to validation run; including not only the custom panel design but also species-specific or sequencer-specific blockers, followed by reagent conditioning to optimize the individual experiment and sequencer.
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The most comprehensive whole exome panel that covers the target regions of all major WES panels in the market. With our proprietary technologies, we provide industry-leading performance and efficiency with complete BI solution.
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Find useful information, insights and tools for your Celemics’ products and services
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Sharing interesting stories about the world of NGS and how Celemics delivers the innovative NGS solutions to the world of science.
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Find useful information, insights and tools for your Celemics’ products and services
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In-silico designed and wet-lab validated exclusive probes to ensure state-of-the-art capture performance
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View Detail >Market-leading performance with minimized PCR bias
NGS 라이브러리 준비 과정에서 Polymerase의 선택은 균일한 커버리지와 안정적인 수율을 확보하는 데 중요한 요소입니다. CLM Polymerase는 PCR bias를 최소화하고, 까다로운 샘플에서도 높은 정확도의 증폭을 가능하게 하도록 설계되었습니다. 또한 모든 PCR 반응에 필요한 구성 요소가 포함되어 있어 연구자가 손쉽게 정확하고 재현성 있는 결과를 얻을 수 있습니다.

CLM Polymerase는 high-GC와 low-GC 영역 모두에서 균일하게 증폭하며, 극단적인 GC 함량을 가진 유전체에서도 coverage bias를 최소화합니다. 90% 이상의 GC 영역(연두색 점선 원)에서 경쟁사 제품은 sequencing depth가 급격히 감소하지만, 셀레믹스의 CLM Polymerase는 고도화된 효소 기술을 기반으로 안정적인 sequencing depth를 유지합니다. 이를 통해 난이도 높은 유전체 영역에서도 신뢰할 수 있는 증폭 성능과 일관된 데이터 품질을 제공합니다.
The amplification capacity was tested using bacterial samples with known GC contents. The results show that CLM Polymerase allows steady and uniform amplification without PCR bias for both high-GC and low-GC regions.
* For GC-ratio analysis, the genomic DNA sequence was partitioned into contiguous 200 bp fragments. The GC content of each fragment was computed, and the resulting values were aggregated into a histogram with 2% interval bins. The green, red, and purple lines represent the normalized sequencing depth across different GC-ratio regions.
최적화된 반응 조건을 통해 CLM Polymerase는 치환(Substitution)과 삽입·결실(Indel)을 포함한 총 오류율을 0.109%로 낮게 유지합니다. 이를 통해 경쟁 제품 대비 더 높은 신뢰성을 제공하며, 후속 분석(Downstream analyses) 과정에서도 안정적인 데이터 품질을 보장합니다.
CLM Polymerase shows the lowest overall PCR error rate (0.109%)
compared to competitor enzymes, minimizing substitutions and indels.
| Polymerase | Sub_ratio | Indel_ratio | Err_ratio |
|---|---|---|---|
| Celemics | 0.068% | 0.041% | 0.109% |
| Company K | 0.068% | 0.048% | 0.116% |
| Taq | 0.112% | 0.040% | 0.153% |
CLM Polymerase는 1 ng에서 100 ng까지 다양한 DNA 양(DNA amount)에서 안정적인 증폭을 제공합니다. 경쟁 효소 대비 일관되게 더 높은 수율(Yield)을 확보하여, 제한된 샘플(Available sample) 조건에서도 유연하게 실험을 진행할 수 있습니다.
A. With 1 ng of DNA, CLM Polymerase achieved an average yield of 1,997 ng after 14 PCR cycles, the highest among competitor enzymes.
B. At 100 ng of DNA, CLM Polymerase maintained the highest average yield of 1,918 ng, demonstrating robust amplification efficiency.
NGS Library Preparation 키트로 셀레믹스의 Target Enrichment 패널에 최적화된 키트

NGS Library Preparation 키트로 셀레믹스의 Target Enrichment 패널에 최적화된 키트

최고 품질의 마그네틱 비드로 사용하기 편리하며 높은 재현성을 보여 NGS 실험에 최적화된 비드

타겟 영역에 결합한 프로브를 Biotin-streptavidin 결합력을 이용하여 농축하기 위해 사용되는 비드

고객의 목적에 맞게 유전자 영역을 자유롭게 구성한 NGS 패널로 시약부터 프로토콜까지 최적화된 패널 제공
Technical Resources
[Product Sheet] Celemics CLM Polymerase
Celemics Target Enrichment Panel Overview
Celemics Products & Services
Safety Data Sheets
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MSDS_CLM Polymerase