Primer and method for detecting CSF3R point mutation

The invention provides a primer and a method for detecting CSF3R point mutation by adopting RT-PCR and a sanger sequencing method. The primer and the detection method can be used for conveniently, economically and accurately diagnosing the mutation situation of CSF3R mutation site genes of a patient...

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Bibliographische Detailangaben
Hauptverfasser: ZOU YUAN, CHEN HONGMEI, DU CUI, ZHU LIANGJUN, XIA CHENGQING
Format: Patent
Sprache:eng
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Beschreibung
Zusammenfassung:The invention provides a primer and a method for detecting CSF3R point mutation by adopting RT-PCR and a sanger sequencing method. The primer and the detection method can be used for conveniently, economically and accurately diagnosing the mutation situation of CSF3R mutation site genes of a patient, have a great guidance signification for treatment and medication of clinical chronic granulocytic leukemia patients, and are helpful for evaluating other agnogenic diseases which take neutrophilic leukocytosis as a characteristic.