搜索





Classic Series Genetic Analyzer

Classic 116/ 108

Superyears Gene Technology company provides Classic series genetic analyzer based on Sanger Sequencing Principle. Superyears has made a breakthrough with the state-of-the-art Eight-color Fluorescence technology and optional 8-,16-,24-,96- (under research) channel analyzer, which can be applied in gene sequencing and fragment analysis. Therefore, it is suitable for basic Molecular Genetic Research, Clinical Medicine, Food Safety, Agricultural Science and other scenarios. Classic 108 and Classic 116 have been approved by NMPA and can be used for in vitro diagnosis.

Superyears Gene Technology company provides Classic series genetic analyzer based on Sanger Sequencing Principle. Superyears has made a breakthrough with the state-of-the-art Eight-color Fluorescence technology and 8,16,24,96 (under research) channel selections instead of using the pervious 6-color technology. It can be utilized in gene sequencing and fragment analysis. Therefore, it is suitable for basic Molecular Genetic Research, Clinical Medicine, Food Safety, Agricultural Science and in some other application scenarios. Classic108 and Classic116 have been approved by NMPA and can be used for in vitro diagnosis.

NMPA:Certification

CE Certification

Classic Series Genetic Analyzer

Product description

Basic Parameters

Performance Parameters

Operating Environment

Gene Sequencing Flux and Performance Index

Fragment Analysis of Flux and Performance Index

Size (L x W x H)	Doors Closed:610 x 532 x 812 mm Doors Opened: 1225 x 532 x 812 mm
Weight	95KG (approx.)
Channel	8, 16, 24, 96 (under research)
Fluorescence Dye	6、8
Capillary Length	36 cm、50 cm
Sampling Method	Auto-Sampling, Compatible with 96-well plate(x2) and 8-strip tubes.
Polymer-Injection Method	Auto-Polymer Injection
Laser	Solid-state semiconductor
Laser wave length	505 nm
Fluorescence Dye wave length	> 520 nm

Size (L x W x H)	Doors Closed:610 x 532 x 812 mm Doors Opened: 1225 x 532 x 812 mm
Weight	95KG (approx.)
Channel	8, 16, 24, 96 (under research)
Fluorescence Dye	6、8
Capillary Length	36 cm、50 cm
Sampling Method	Auto-Sampling, Compatible with 96-well plate(x2) and 8-strip tubes.
Polymer-Injection Method	Auto-Polymer Injection
Laser	Solid-state semiconductor
Laser wave length	505 nm
Fluorescence Dye wave length	> 520 nm

Temp. Accuracy	ΔT≤0.2℃
Resolution Ratio	0.15 bp
Detection Capability	Above 850 bp
Fluorescence Dye wavelength	> 520 nm

Power	220±10% VAC，50±1 Hz; Single Phase: 10 A，2200 VA
Ambient Temperature	15℃~30℃, Temperature Uniformity ±2℃
Relative Humidity	20%~80%
Atmospheric Pressure	86 kPa~106 kPa

Operational Mode	Average running time (min)	Max.Flux (Sample/Day)	Capillary Length(cm)	Polymer type	Continuous Reading Length (CRL)（CRL）
Sequence36_SY07	35	656	36	SY07	500 bp
Sequence50_SY07	120	192	50	SY07	850 bp
Fastseq50_SY07	60	384	50	SY07	700 bp

Operational Mode	Average running time (min)	Max.Flux (Sample/Day)	Capillary Length(cm)	Polymer type	Continuous	Reading	Length (CRL) 50-400 401-640 640-1200
GeneScan36_SY04	50	448	36	SY04	40-640 bp	640 bp	<0.15	<0.3	N/A
GeneScan36_SY07	35	656	36	SY07	40-640 bp	640 bp	<0.15	<0.3	N/A
GeneScan50_SY07	45	512	50	SY07	40-640 bp	640 bp	<0.15	<0.3	N/A
GeneScan50_SY07Long	125	176	50	SY07	40-1200 bp	1200 bp	<0.15	<0.3	<0.35

None

Accuracy

“Gold Standard” sequencing, accuracy rate 99.99%

High efficiency

6-color,8-color Fluorescence, and max. of 70 STR loci can be detected in a single test

Economic

Cost-effective product and consumables, Free software update

Compatibility

Open platform, compatible with mainstream reagent kits and consumables

Customizable

Customized interface, easy to interact, handy to operate

Accuracy

“Gold Standard” sequencing, accuracy rate 99.99%

High efficiency

6-color,8-color Fluorescence, and max. of 70 STR loci can be detected in a single test

Economic

Cost-effective product and consumables, Free software update

Compatibility

Open platform, compatible with mainstream reagent kits and consumables

Customizable

Customized interface, easy to interact, handy to operate

Technical Parameter

Classic Series Genetic Analyzer

Superyears Gene Technology company provides Classic series genetic analyzer based on Sanger Sequencing Principle. Superyears has made a breakthrough with the state-of-the-art Eight-color Fluorescence technology and 8,16,24,96 (under research) channel selections instead of using the pervious 6-color technology. It can be utilized in gene sequencing and fragment analysis. Therefore, it is suitable for basic Molecular Genetic Research, Clinical Medicine, Food Safety, Agricultural Science and in some other application scenarios. Classic108 and Classic116 have been approved by NMPA and can be used for in vitro diagnosis.

产品描述

[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[产品参数, 参数]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]

Basic Parameters

Performance Parameters

Operating Environment

Gene Sequencing Flux and Performance Index

Fragment Analysis of Flux and Performance Index

Size (L x W x H)	Doors Closed:610 x 532 x 812 mm Doors Opened: 1225 x 532 x 812 mm
Weight	95KG (approx.)
Channel	8, 16, 24, 96 (under research)
Fluorescence Dye	6、8
Capillary Length	36 cm、50 cm
Sampling Method	Auto-Sampling, Compatible with 96-well plate(x2) and 8-strip tubes.
Polymer-Injection Method	Auto-Polymer Injection
Laser	Solid-state semiconductor
Laser wave length	505 nm
Fluorescence Dye wave length	> 520 nm

扫二维码用手机看

上一个

[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[无, 无]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]], [[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[[无, 无]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]]

下一个

Consumable Reagent

Consumable Reagent	Specification Model	Unit	Code
16-Channel Capillary tube	36 cm	set	SY01C001
16-Channel Capillary Capillary Array	50 cm	set	SY01C002
10x buffer	500 ml	Bottle	SY01C010
HD formamide	25 ml	Bottle	SY01C008
SY04 Polymer	3.5 ml	Bottle	SY01C005
SY07 Polymer	28 ml	Bottle	SY01C006

Product Application

Cardiovascular

Infectious Disease

Oncology Department

Reproductive Genetics

Endocrinology Department

Hematology Department

Urology Department

Diseases/Drugs	Detection Items	Clinical Significance
Clopidogrel	CYP2C19	Guarantee the safety and effectiveness of Clopidogrel
Aspirin	COX1、GP1BA、LTC4S	Evaluation of the resistance risk of Aspirin
Warfarin	CYP2C9、VKORC1	Guidance of the usage measurement of Warfarin
Five types of Antihypertensive	ADRB1、CYP2D6、NPPA、CYP3A5、CYP3A4、ACE、CYP2C9	Rational use of antihypertensive drugs
Statins	SLCO1B1、ApoE	Individualized treatment in accordance with the genetype
Nitroglycerin	ALDH2	The instruction of using Nitroglycerin
Homocyste ine	MTHFR	High homocysteine levels are associated with a higher risk of cardiovascular disease

Diseases/Drugs	Detection Items	Clinical Significance
Hepatitis C	Genotyping of hepatitis C virus	Determine the illness,Assist in determining treatment options
Hepatitis B	Hepatitis B virus drug resistance gene	Guidance of using medicine for Hepatitis B
Tuberculosis (TB)	Isoniazid resistance gene of Mycobacterium tuberculosis	Guidance of using Medicine for clinic
Tuberculosis (TB)	Mycobacterium tuberculosis is resistant to rifampicin	Guidance of using Medicine for clinic
Human papillomavirus infection	HPV genotyping	Early detection of HPV infection
Multiple respiratory infections	Common a variety of respiratory tract infection, respiratory tract bacteria, virus detection	Auxiliary diagnosis and differential diagnosis of respiratory tract infection
HIV/AIDS	Detection of drug resistance genotypes of human immunodeficiency virus type 1 (HIV-1)	Guidance for medicine using resistance

Diseases/Drugs	Detection Items	Clinical Significance
Glioma	IDH1, IDH2, TERT gene	Classification and prognosis of glioma
Non-brainstem glioma/giant cell tumor of bone	H3F3A, H3F3B genes	Assist in the diagnosis of non-brainstem glioma and giant cell tumor of bone
Gastrointestinal stromal tumor	KIT gene, PDGFRa gene	Efficacy of tyrosine kinase inhibitors. Prognostic assessment of disease
Breast cance	HER2, PIK3CA, CYP2D6, BRCA1/2 genes	Prediction of disease risk, prognosis and effective treatment plan
Non-small cell lung cancer	EGFR, K-RAS, B-Raf genes	Predicting the efficacy of targeted drugs; Prognostic evaluation of disease
Colorectal cance	K-ras, B-Raf, n-Ras genes	Prognosis evaluation and medication guidance
Targeted drugs/sorafenib, sunitinib, pazopani, bevacizumab, erlotinib, etc	PDGFRβ, VEGFR1, VEGFR2, EGFR, K-ras, B-Raf, PIK3CA, TTF-1, KIT, etc	Guidance for using targeted medicine
Chemotherapy drugs/platinum, taxus, fluorine, gemcitabine, purine, etoposide, teniposide, etc	ERCC1, ABCC2, XRCC1, GSTM1, XPD, GSTT1, GSTP1, BRCA1, etc.	Predict drug efficacy and reduce toxic and side effects
Irinotecan	UGT1A1 gene	Predict drug efficacy and reduce toxic and side effects

Diseases/Drugs	Detection Items	Clinical Significance
Trisomy 21 syndrome, Klinefelter syndrome, superfemale syndrome	Chromosome (13/18/21/X/Y) multiple STR genotyping	Prenatal and prenatal auxiliary diagnosis
Duchenne muscular dystrophy	DMD gene exon deletion, and repeat mutation detection	Differential diagnosis, prenatal screening
Brittle syndrome	Fragile X syndrome high-risk gene screening	Diagnosis and establishment of diagnosis, prenatal screening
Spinal muscular atrophy	Mutation detection of SMN1 and SMN2 genes	Prenatal genetic screening
Phenylketonuria	Detection of phenylketonuria gene mutation	Confirming diagnosis and directing treatment; eugenics
Deafness	Genetic testing for hereditary deafness	Genetic screening for neonatal deafness
Anemia	Detection of missing type α/β thalassemia (MLPA)	The differential diagnosis
Wilson's disease	ATP7B gene	Etiological diagnosis and early treatment; eugenics

Diseases/Drugs	Detection Items	Clinical Significance
Adolescent onset of adult type diabetes	GCK, HNF1A, HNF4A, HNF1B, PDX1, NEUROD1 genes	Differential diagnosis of diabetes type and guidance of using medicine
Susceptibility to type 1 diabetes	MHC, CTLA4, TSHR genes	The great significant to evaluate the risk of GD
Papillary thyroid carcinoma, medullary thyroid carcinoma	RET gene	RET gene mutation is the molecular pathological basis of MTC
Multiple endocrine neoplasm	MEN1, RET gene	Prenatal diagnosis and provide the risk evaluation
Abnormal lipid metabolism	LDLR, APOB, LPL, ApoC ⅱ, ABCA1, ApoC ⅰ, ApoC ⅲ, ApoC ⅳ, ApoC ⅴ genes	Effective screening of carriers, auxiliary diagnosis, early treatment
Diabetes	OCT2、CYP2C9、PPARγ、SLCO1B1	Personalized guidance of using medication
Congenital adrenal hyperplasia	CYP21A2 gene	Auxiliary diagnosis
Hyperuricemia, gout	HLA-B 5801	NCCN guidelines recommend hLA-B 5801 gene testing before allopurinol

Diseases/Drugs	Detection Items	Clinical Significance
Primary test for acute myeloid leukemia (AML)	FLT3, KIT, TP53, RUNX1, CEBPA, ASXL1, NPM1, IDH1, IDH2 genes	Assist in diagnosis, medication guidance and prognosis assessment
Primary test for acute myeloid leukemia (AML)	DNMT3A, SF3B1, U2AF1, SRSF2, EZH2, WT1 genes	Assist in diagnosis, prediction of disease progression and prognosis assessment
Acute lymphoblastic leukemia (ALL)	BCR/ABL1, CRLF2, IKZF1, PRPS1, SH2B3, IL7R genes	Assist in diagnosis, prediction of disease progression and prognosis assessment
Primary myelofibrosis (PMF)	JAK2, MPL, ASXL1, EZH2, IDH1, IDH2, SRSF2, U2AF1, TP53 genes	Assist in diagnosis and condition evaluation
Polycythemia vera (PV)	JAK2, ASXL1, IDH1, IDH2, SRSF2 genes	Assist in diagnosis and prognosis
Primary thrombocytopenia (ET)	CALR、MPL、ASXL1、EZH2、SRSF2、U2AF1、TP53、SF3B1 genes	Assist in diagnosis, prognosis and progression
Myelodysplastic syndrome (MDS)	DNMT3A, ASXL1, EZH2, SF3B1, SRSF2, U2AF1, TP53, NRAS genes	Assist in diagnosis, prognosis and progression
Lymphocytic lymphoma/Fahrenheit macroglobulinemia (LPL/WM)	MYD88, CXCR4 gene	Auxiliary diagnostic LPL/WM
Chronic neutrophil leukemia (CNL)	CSF3R gene	Deterministic molecular abnormalities of CNL and atypical CML

Diseases/Drugs	Detection Items	Clinical Significance
Parkinson's disease.	11 Parkinson's disease genes including SNCA	Genetic screening and early diagnosis of Parkinson's disease
Depression	CYP2D6 and four other genes	Guidance on antidepressant medication
Epilepsy	POLG and four other genes	Guidance of antiepileptic drugs
Mania	Two loci on GSK3B and NTRK2 genes associated with antimanic drugs	Guidance of using medicine for mania
Meningitis/encephalitis	Simultaneous detection of multiple encephalitis and meningitis pathogens	Etiological diagnosis of encephalitis and meningitis
Mental illness	SLC6A2 and 6 other genes	Guidance of using medicine for antipsychotic medication

Nanjing Superyears Gene Technology Co., Ltd.

Hotline：

（0086）400-677-8378

Address：

Room 1501, Chengxian Building, No.50 Chengxian Street, Xuanwu District, Nanjing, Jiangsu Province.

Room 1105/F11, Block 3-2B, 88 Pubin Avenue, Jiangpu Street, Pukou District, Nanjing

Please Submit Online Request
Our staff will contact you within 24 hours (working days). If you need other services, please call the service hotline: 400-677-8378

* Message contents：

Name：

Mobile phone：

E-mail：

Address：

Postal code：

全部评论

已有0条评论

There is currently no content to display