Protocol for purification of cells in their native state using reversible aptamer-antidote pairs.

Protocol for purification of cells in their native state using reversible aptamer-antidote pairs.
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DOI:
10.1016/j.xpro.2023.102348
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发表时间:
2023-09-15
期刊:
影响因子:
--
通讯作者:
Sullenger, Bruce A.
Sullenger, Bruce A.
中科院分区:
其他
文献类型:
--
作者:
Requena, Martin D.;Gray, Bethany Powell;Sullenger, Bruce A.

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Cell isolation from complex mixtures is a key step in many clinical and research applications, but standard isolation methods may affect the cell’s biology and are difficult to reverse. Here, we present a method to isolate and restore cells to their native state using an aptamer that binds epidermal growth factor receptor (EGFR+)cells and a complementary antisense oligonucleotide to reverse binding. For complete details on the use and execution of this protocol, please refer to Gray et al. High-purity isolation of specific cell types and viable cells Cells are returned to their native state post-purification Adaptable for use with different aptamer-antidote pairs Adaptable for use with blood, homogenized tissue, or other complex cell mixtures Publisher’s note: Undertaking any experimental protocol requires adherence to local institutional guidelines for laboratory safety and ethics. Cell isolation from complex mixtures is a key step in many clinical and research applications, but standard isolation methods may affect the cell’s biology and are difficult to reverse. Here, we present a method to isolate and restore cells to their native state using an aptamer that binds epidermal growth factor receptor (EGFR+) cells and a complementary antisense oligonucleotide to reverse binding.
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