Department of Life Science and Medical Bioscience, Waseda University, Shinjuku-ku, Japan.
Leuk Res. 2011 Dec;35(12):1632-6. doi: 10.1016/j.leukres.2011.06.016. Epub 2011 Jul 12.
We developed a simple, cost-effective, and accurate JAK2 allele burden quantification method named alternately binding probe competitive PCR (ABC-PCR). ABC-PCR can be performed to quantify target JAK2 allele burdens in a single reaction. The throughput and running cost of ABC-PCR are markedly improved compared with those of allele-specific quantitative PCR (AS-qPCR). The quantification of samples with known JAK2 allele burdens revealed that ABC-PCR had a small assay-to-assay variation. The JAK2 allele burdens in the patients with myeloproliferative neoplasms measured by ABC-PCR and AS-qPCR showed a good fitting. ABC-PCR would be a powerful tool for quantifying target JAK2 allele burdens.
我们开发了一种简单、经济、准确的 JAK2 等位基因负担定量方法,命名为交替结合探针竞争 PCR(ABC-PCR)。ABC-PCR 可以在单个反应中定量目标 JAK2 等位基因负担。与等位基因特异性定量 PCR(AS-qPCR)相比,ABC-PCR 的通量和运行成本显著提高。对具有已知 JAK2 等位基因负担的样本进行定量分析表明,ABC-PCR 的测定值具有较小的批间差异。通过 ABC-PCR 和 AS-qPCR 测量的骨髓增殖性肿瘤患者的 JAK2 等位基因负担显示出良好的拟合度。ABC-PCR 将成为定量目标 JAK2 等位基因负担的有力工具。