Product

NgeneBio – SOLIDaccuTest™

SOLIDaccuTest™ is an excellent tool for discovering variants associated with solid tumors using a comprehensive approach to next-generation sequencing (NGS). It reflects the latest research trends and is optimized for medical purposes by selecting essential genes of solid tumors including lung, colon, breast, skin brain, stomach and ovarian cancers, etc.

Solution: NgeneBio – SOLIDaccuTest™

SOLIDaccuTest™ is an excellent tool to explorer variants associated with solid tumors using a comprehensive method of next-generation sequencing (NGS). It reflects the latest research trends and is optimized for the medical purpose by selecting essential genes of solid tumors including lung, colon, breast, skin brain, gastric, ovarian cancers, etc.

 

BRCAaccuTest™ & BRCAaccuTest™PLUS

BRCAaccuTest™ PLUS with CE-IVD certificate for HBOC Breast/Ovarian Cancer Test

BRCAaccuTest™ & BRCAaccuTest™PLUS

BRCAaccuTest™ & BRCAaccuTest™PLUS is a regent for producing libraries for
analyzing the BRCA ½ genes using the NGS (next-generation sequencing) method,
which analyzes genomic DNA derived from blood or FFPE tissues.

Next Generation Sequencing System – NovaSeq 6000

Model: NovaSeq 6000
Manufacturer: Illumina/USA
– Scalable platform
Match data output, time to results, and price per sample to study needs
– Flexible performance
Configure sequencing method, flow cell type, and read length to support a broad range of applications
– Streamlined operation
Increase lab efficiency with a simplified workflow and reduced hands-on time

Next-Generation Sequencing System – NextSeq 2000

 The NextSeq 2000 Sequencing System uses patterned flow cells similar to those that power the NovaSeq™ 6000 System. The result is a highly flexible and scalable benchtop system that offers the highest cluster density flow cell of any on-market NGS system to date, driving down the cost per gigabase (Gb) of the sequencing run.

NextSeq 1000 sequencing system

Product Information

Model: NextSeq 1000

Manufacturer: Illumina

Origin: Singapore/United States

Launching year: 01/2020

PANARealTyperTM HPV Screening Kit

PANARealTyperTM HPV Screening Kit is an in vitro diagnostic kit for the determination of the presence or absence of HPV virus (Human papilloma virus) using a peptide nucleic acid (PNA) probe.

PANARealTyperTM HPV Kit

PANARealTyperTM  HPV Kit is an in vitro diagnostic kit for genotyping of the HPV virus (Human papilloma virus) using a peptide nucleic acid (PNA) probe. The kit is designed to amplify DNA for quantitative detection of a total of 40 HPV strains by Real-time PCR system. The kit provides genetic information of 20 high-risk strains and 2 low-risk strains by analyzing the melting temperature Tm. Moreover, the kit can also screen 18 other genotypes (no genotypes are named) in clinical samples.

DxFLEX

DxFLEX is a new clinical flow cytometry platform derived from the successful CytoFLEX. The advanced sensitivity and intuitive software DxFLEX makes flow cytometry routine for both novice and expert flow cytometry technicians and promotes standardization. Functionality in the autoloader facilitates accurate results and sample tracking.

 

CytoFLEX

Model: CytoFLEX
Manufacturer: Beckman Coulter Life Sciences/ USA

The CytoFLEX Flow Cytometer is the most innovative flow cytometer system of Beckman Coulter. With compact design and high efficiency in work, CytoFlex provides and easy to use system with the impressive performance you need. Our system allows the researchers just focus on the science with no worry about instrument. Its superior sensitivity and resolution throughout all configurations give it the edge over other cytometry systems four times its size.

– Up to 3 lasers Violet-Blue-Red (V-B-R) and fully activated with 13 colors

– Ability to measure 100 nm particles with violet laser

– Includes 13 band pass filters: 450/45, 525/40 (2), 585/42, 610/20 (2), 660/10 (2), 690/50, 712/25, 780/60 (3)

– For higher throughput applications an optional plate loader module is available

– Smart software in acquisition and analysis CytExpert

Next-Generation Sequencing System – NovaSeq 6000

Model: NovaSeq 6000
Manufacturer: Illumina/USA
– Scalable platform
Match data output, time to results, and price per sample to study needs
– Flexible performance
Configure sequencing method, flow cell type, and read length to support a broad range of applications
– Streamlined operation
Increase lab efficiency with a simplified workflow and reduced hands-on time

Next Generation Sequencing System – iSeq 100

Model: iSeq 100
Manufacturer: Illumina/USA
Illumina’s smallest next-generation DNA sequencing system, with small, fast and efficient sequencing throughput, suitable for all labs
– Fast data generation: Suitable for small projects, on a dedicated device, low throughput with fast turnaround times
– Convenient operation: Control the sequencing process from start to finish and ensure independent sequencing instead of outsourcing.

TruSight® Tumor 26

TruSight Tumor 26 Kit includes library preparation reagent set and uses next-generation sequencing (NGS) technology to provide a comprehensive assessment of 26 genes that are commonly related to mutations in solid tumors and somatic variants

TruSight Cancer Sequencing Panel

Developed with cancer genomics experts in collaboration, oligos ready-to-use, pre-engineered oligos allow researchers to sequence a wide range of genes and single nucleotide polymorphisms (SNPs) in advance. this is related to cancer predisposition

TruSight Tumor 26

TruSight Tumor 26 Kit include reagents to prepare for Library preparation samples, sequencing 26 genes relating to solid cancer, variant of  soma in NGS – Next Generation Sequencing of Illumina

Next Generation Sequencing System – NextSeq 550

Model: Nextseq 550
Manufacturer: Illumina/USA
– Is the only sequencing system capable of deploying applications running sequencing and reading microarray biochips
– New generation DNA sequencing system using synthetic sequencing technology: Sequencing by Synthesis – SBS
– The whole process of gene sequencing is conducted on the surface of flow cells, convenient to use and easy to manipulate.

Next Generation Sequencing System – MiSeq

Model: MiSeq
Manufacturer: Illumina/USA
– The MiSeq System combines cluster generation, amplification, sequencing and data analysis on a single system
– The system is most widely used, with next-generation sequencing technology –  Sequencing by Synthesis – SBS

Next Generation Sequencing System – MiniSeq

Model: MiniSeq
Manufacturer: Illumina/USA
– New generation DNA sequencing system using synthetic sequencing technology: Sequencing by Synthesis – SBS
– Next Generation Sequencing, allowing to run the entire DNA and RNA amplification process combined with sequencing analysis on a single system
– Maximum reading capacity: 7.5 Gb (equivalent to 7.5 billion bases) within 24 hours
– Data Quality (Quality Score) > Q30 (accuracy 99.9%)

EGFR gene – Mutation detection Kit

Code: PNAR-3001

Packing: 24 Pounds/set

Certificate: CE-IVD

PANAMutyper™ NRAS

Code: PNAR-2001

Packing: 24 Pounds/set

Certificate: CE-IVD

PANAMutyper™ KRAS

Code: PNAR-1001

Packing: 24 Pounds/set

Certificate: CE-IVD

PNAClamp™ EGFR (ver.2)

Code: PNAC-3002

Packing: 25 tests/set

Certificate: CE-IVD

PNAClamp™ EGFR Mutation Detection Kit (ver.2)

Code: PNAC-3002

Packing: 25 tests/set

Certificate: CE-IVD

PNAClamp™ KRAS (ver.4)

Code: PNAR-1006

Packing: 25 Pounds/set

Certificate: CE-IVD

PNAClamp™ NRAS Mutation Detection Kit

 

Code: PNAC-1101 (43 mutations)

Packing: 25 tests/set

Certificate: CE-IVD

PNAClamp™- PIK3CA Mutation detection Kit

The PNAClamp™ PIK3CA Mutation Kit utilizes PNA-mediated Real-time PCR clamping – an innovative PCR technology that uses optimally designed PNA probes that bind to the wild-type DNA template (DNA that does not contain mutation).