Human MTHFR Gene Detection Kit (Fluorescent PCR Method)
This product is suitable for qualitative detection of MTHFR C677T gene polymorphism in human whole blood samples in vitro.
Successfully obtained in the EU CE access certification.
DESCRIPTION
Main clinical applications:
1. Prevention of birth defects
Screening for high-risk groups prone to folic acid deficiency, personalized folic acid supplementation program to prevent birth defects.
2.Eugenics
Individualized folic acid supplementation for pregnant women and fertile women/men to reduce the risk of infertility and adverse pregnancy outcomes.
3.H-type hypertension and cardiovascular disease risk
MTHFR 677TT genotype is a risk factor for coronary heart disease and stroke. MTHFR genotype testing for hypertensive patients can help to stratify the risk and avoid the occurrence of serious cardiovascular and cerebrovascular events.
4.Tumor drug guidance
To help clinics formulate individualized treatment plans, predict and reduce the adverse effects of tumor drugs such as 5-fluorouracil and methotrexate.
Applicable Instruments：
HONGSHI SLAN-96, ABI 7500, and other four-channel fluorescence PCR instruments.
SPECIFICATION
1.High sensitivity
Unique nucleic acid invasion signal amplification technology, the lowest detection limit of 0.2 ng/µL.
2.Wide detection range
0.2 ng/µL - 100 ng/µL.
3.Lyophilized reagent
Good stability, no need for cold chain transportation, cost saving;
4.Convenient operation
The whole premixed dispensing, ready to use, no need to dispense liquid.
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