Hmoe > CDO > QPCR
QPCR
Molecular diagnosis refers to the application of molecular biological methods to detect changes in the structure or expression level of genetic material in patients. Molecular diagnosis is the main method of predictive diagnosis, which cannot only diagnose individual genetic diseases, but also prenatal diagnosis. Molecular diagnosis mainly refers to the detection of genes encoding various structural proteins, enzymes, antigens, antibodies and immune active molecules related to diseases.

The main methodologies of molecular diagnosis include QPCR/RT-QPCR, NGS, LAMP, FISH, etc. In particular, QPCR/RT-QPCR is the most important methodology used in molecular diagnosis . With the global spread and outbreak of COVID-19, COVID-19 nucleic acid detection has been widely recognized and accepted worldwide. QPCR/RT-QPCR technology used for detection still has considerable technical barriers and difficulties in the development of in vitro diagnostic reagents.

DxPartner has already owned all the process techniques from new product research and process optimization to large-scale production and manufacturing in its own facility, which can provide high-quality and stable materials and solutions for the specific needs of customers with effectiveness and cost-effectiveness. The following are the relevant biomarkers of QPCR/RT-QPCR platform that can be developed by DxPartner. For more information, pleasecontact us

QPCR/RT-QPCR

Infectious Disease

Group B streptococcal

Respiratory syncytial viruses A/ B

Dengue virus

Epstein-Barr virus

Novel coronavirus 2019-nCoV/influenza A(B) virus

Gonococcus/Chlamydia trachomatis/ureaplasma urealytica

Mycobacterium tuberculosis

Hepatitis C virus

HPV  (16/18/52/58/33 type)

Influenza A/B virus

Hepatitis B virus

Enterovirus generic / enterovirus 71 / Coxsackievirus A16

Mycoplasma pneumoniae/Chlamydia pneumoniae


Cancer

ALK gene/ROS1 gene

MGMT gene-methylation

SDC2 gene-methylation

Mutation of the BRAF gene V600E

miR-92a

Septin9 gene-methylation

EGFR/ALK/ROS1 gene-mutant type

MTHFR gene-mutant type

SHOX2/RASSF1A gene-methylation

EML4-ALK fusion gene

NRAS gene-mutant type

TERT gene promoter-mutant type

IDH1 gene-mutant type

PIK3CA gene-mutant type

UGT1A1 gene-polymorphism

JAK2-V617F gene-mutant type

RNF180/Septin9 gene- methylation

Leukemia-associated fusion genes

KRAS/NRAS/PIK3CA/BRAF gene-mutant type

ROS1 gene

MicroRNA

KRAS gene- 8 mutant types


New Born Screening

Herpes simplex virus  type I

Measles virus/rubella virus

Aminoglycosides are deafening susceptibility genes

Herpes simplex virus type II

Legionella pneumophila

α- Thalassemia gene-Non- deletion type

Types I and II herpes simplex virus

Methylenetetrahydrofolate reductase gene 677C/T

α- Thalassemia gene-deletion type

Rubella virus

PDS gene mutations

Drug-induced deafness gene-mutant type

Cytomegalovirus

Y chromosome microdeletions

Hereditary deafness gene


Cardiac Disease

CYP2C9 gene mutation

VKORC1 gene-mutant type


Cardiovascular

ALDH2 gene-polymorphism


Digestive disease

Helicobacter pylori


AD

Human APOE gene

Human SLCO1B1 gene


Hypertension

CYP2D6 gene- polymorphism

AGTR1 gene-polymorphism

ACE gene- polymorphism

CYP2C9 gene- polymorphism


Blood lipid

 ApoE and SLCO1B1 gene-Polymorphisms


Gynecological disease

Candida albicans


Clinial Microbiology

Salmonella/Shigella bacteria


Therapeutic drugs

HLA-B*15: 02 gene

Enquiry

Headquarter

Office: 341 Yanhe West Rd, Xiangzhou District, Zhuhai, Guangdong
Facility: No. 21, Shanbianhong East Rd, Haicang District, Xiamen, Fujian
Hot Line: 400-880-1039
Email: customerservice@dxpartner.cn

法律声明 | 合作模式 | 新闻中心

网站备案 / 许可证号:粤ICP备2022130380号-1 / Copyright © 2010-2023 DxPartner All rights reserved

Contact Us