Nanjing Superyears Gene Technology Co., Ltd.

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Home > Products > Molecular Biolab Equipment > Fragment Analysis Instrument > Capillary Fragment Analysis Genetic Analyzer

Capillary Fragment Analysis Genetic Analyzer

Payment Type:
T/T
Incoterm:
FOB,CIF,EXW,Express Delivery
Min. Order:
1 Pack/Packs
Transportation:
Ocean,Land,Air,Express
Port:
Shanghai
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  • Product Description
Overview
Product Attributes

Model No.Classic 116 Genetic Analyzer

BrandClassic Series

Types OfGenes &Amp; Life Science Equipments

Place Of OriginChina

Medical Device ClassificationClass Ii

Warranty Service2 Years

After-sales ServiceOnsite Training, Free Spare Parts, Online Technical Support, Onsite Installation, Return And Replacement

Supply Ability & Additional Information

PackagingWooden package

Productivity30 units per month

TransportationOcean,Land,Air,Express

Place of OriginCHINA

Supply Ability10 Packages

CertificateISO13485

HS Code902750020

PortShanghai

Payment TypeT/T

IncotermFOB,CIF,EXW,Express Delivery

Packaging & Delivery
Selling Units:
Pack/Packs
Package Type:
Wooden package
Picture Example:

Capillary Fragment Analysis Genetic Analyzer


DNA Analyzer Description

Superyears Classic Series are developed upon Sanger Method, which could support up to 6-color or 8-color fluorescence and be applied to gene sequencing and fragment analysis. Therefore, it could attend to basic research and clinical laboratory use needs. The Classic series gene analyzer comprises a capillary electrophoresis host, computer, matching consumables materials and reagents, and self-developed data acquisition and data analysis software. The data acquisition software provides a customizable operation interface, which can reflect the running status of the instrument, the usage status of consumables materials, and systematic maintenance in real-time; The data analysis software consists of sequencing analysis software and fragment analysis software. The sequencing analysis software can be used for base-calling, sequencing data quality evaluation, mutation spot search, automatic deletion of low-quality data, and other functions; The fragment analysis software can be used to analyze STR, SNP, AFLP, Fusion, Rearrangement, etc.


Forensic Testing Dna Sequencer Advantages

1.Based upon Sanger Method, Outstanding performance of the golden standard;
2.Support up to 8-color fluorescence, single detection for  more than 70 sites;
3.High resolution, High repeatability and Outstanding sequencing quality;
4.Completely open detection platform, compatible with commercial kits in the market;
5.Language interface customizable, free charge of software upgrading;
6.High-cost performance, saving 50%+ of cost in consumables materials and reagents;
7.Certificated by China National Medical Products Administration (NMPA)  and CE, ensuring 

Dna Fragment Analyzer Advantages

1.Based upon Sanger Method, Outstanding performance of the golden standard;
2.Support up to 8-color fluorescence, single detection for  more than 70 sites;
3.High resolution, High repeatability and Outstanding sequencing quality;
4.Completely open detection platform, compatible with commercial kits in the market;
5.Language interface customizable, free charge of software upgrading;
6.High-cost performance, saving 50%+ of cost in consumables materials and reagents;
7.Certificated by China National Medical Products Administration (NMPA)  and CE, ensuring in vitro diagnostic (IVD) applicable;
8.Perfect technical support and after-sale services, one year of free warranty;

Automatic Gene Analyzer Application

Disease Area

Clinical Testing Items

Reproductive health

˙ Trisomy 21 and sex chromosome poploidy

˙ Y chromosome microdeletion

˙ Folate metabolism

˙ Fragile X syndrome

˙ HPV genotyping … …

Infectious Disease

˙ Accurate use of infectious diseases (hepatitis B, hepatitis C, Tuberculosis, HIV)

˙ Respiratory tract infection

˙ Diarrhea … …

Tumor

˙ Tumor targeting Medicine (EGFR, KRAS, BRAF, C-KIT, ALK, ROS1, NRAS, PDGFRA, PIK3CA, P53, BRCA1/2, …)

˙ Chemotherapy MedicineUGT1A1, DPD, 5-Fu Medication, platinum Medication Guidance)

˙ Microsatellite instability MSI … …

Hereditary Disease

˙ Neonatal jaundice (UGT1A1)

˙ Hereditary genetic deafness

˙ Dravet syndrome (SCN1A)

˙ HLA typing … …

Blood Disease

˙ Classification, auxiliary diagnosis and treatment of blood diseases, treatment planning / reference, prognosis evaluation (AML, ALL, CLL, CML, MPN, MDS…) … …

Cardio Cerebrovascular

˙ Alcohol metabolism / nitroglycerin efficacy (ALDH2)

˙ Medication guidance (clopidogrel, warfarin) (CYP2C9 / VKORC1) … …


ALL INFORMATION UPATED ON 12/MAY/2022 BY MARKETING TEAM FROM SUPERYEARS CO. 

Product Categories : Molecular Biolab Equipment > Fragment Analysis Instrument

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Tel:0086-025-57561788

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