Customization: | Available |
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Type: | IVD Reagent |
Intended Use: | Leukemia Gene Jak2 V617 Mutation |
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INTENDED USE
The JAK family is a class of non-receptor tyrosine protein kinases, including 4 types of JAK, JAK1, JAK2, JAK3 and TYK2. Some growth factors and most cytokines can activate signal transducers and activators of transcription (STAT) through JAK, thereby affecting gene transcription regulation. JAK-STAT signal transduction pathway is involved in many important biological processes such as cell proliferation, differentiation, apoptosis and immune regulation. Some mutations in JAK2 gene continue to activate the JAK-STAT pathway, which is the cause of tumorigenesis.
Myeloproliferative diseases (MPD) mainly include polycythemia vera (PV), essential thrombocythemia (ET) and primary myelofibrosis (IMF). It has been confirmed that about 90% of PV and 50% of ET and IMF patients have JAK2 gene V617F point mutation, JAK2 gene mutation detection can be used for the diagnosis of MPD. At present, the World Health Organization (WHO) has included it in the diagnostic criteria of MPD.
TEST PRINCIPLE
The kit adopts ARMS-qPCR method to detect JAK2 V617 codon hot spot mutations.
Design primers and specific probes based on the basic principles of fluorescent PCR to detect the target in a targeted manner, and determine the number (concentration) difference between the analytes in the original sample by analyzing the results after amplification.