MTHFR gene mutation caused by the corresponding reduction of enzyme activity can inhibit the conversion of homocysteine to methionine, leading to hypofolatemia and hyperhomocysteinemia.
Through genetic testing technology, the detection of human MTHFR gene can find out the absorption and utilization level of folic acid of different individuals as early as possible, so as to screen out the high-risk groups that are prone to folic acid deficiency, and realize the personalized supplement of folic acid.
Human MTHFR Genotyping Kit (PCR-Fluorescent Probe)
Sample type: whole blood
• No conventional nucleic acid extraction process is required.
• Reagent component integration, simple and quick operation.
• The test can be done with just a small liter of blood sample.
• High specificity and sensitivity.
• Hypertensive patients with elevated homocysteine
• People who need folic acid supplements
This Human MTHFR Genotyping Kit is suitable for Cayudi Biotech Mini8 Plus, ABI 7500, Roche LightCycler 480 real-time quantitative PCR instrument.
