Tumor dissociation of highly viable cell suspensions for single-cell omic analyses in mouse models of breast cancer.

Tumor dissociation of highly viable cell suspensions for single-cell omic analyses in mouse models of breast cancer.
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DOI:
10.1016/j.xpro.2021.100841
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发表时间:
2021-12-17
期刊:
影响因子:
--
通讯作者:
Valdes-Mora F
Valdes-Mora F
中科院分区:
其他
文献类型:
--
作者:
Rodriguez de la Fuente L;Law AMK;Gallego-Ortega D;Valdes-Mora F

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Cell preparation with a high rate of viable cells is required to obtain reliable single-cell transcriptomic and epigenomic data. This protocol describes a technique for digestion and single-cell isolation from mouse mammary tumors to achieve ∼90% of viable cells, which can be subsequently processed in a diverse array of high-throughput single-cell “omic platforms,” both in an unbiased manner or after selection of a specific cell population. For complete details on the use and execution of this protocol, please refer to. Protocol yields cell suspensions with 90% of live cells from mouse mammary tumors Necrosis and lymph nodes can bias the cell composition in breast tumors Single-cell multiomic workflows require highly viable cell suspensions Antibody-based cell selection (MACS or FACS) are compatible methods for cell selection Cell preparation with a high rate of viable cells is required to obtain reliable single-cell transcriptomic and epigenomic data. This protocol describes a technique for digestion and single-cell isolation from mouse mammary tumors to achieve ∼90% of viable cells, which can be subsequently processed in a diverse array of high-throughput single-cell “omic platforms,” both in an unbiased manner or after selection of a specific cell population.
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