<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Gao M</submitter><funding>Technology Innovation Project of Chengdu New Industrial Technology Research Institute</funding><funding>National Natural Science Foundation of China</funding><funding>Department of Science and Technology of Sichuan Province</funding><pagination>23156-23169</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9280780</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(27)</volume><pubmed_abstract>One of the key steps of using CRISPR/Cas9 to obtain gene-edited cells used in generating gene-edited animals combined with somatic cell nuclear transplantation (SCNT) is to harvest monoclonal cells with genetic modifications. However, primary cells used as nuclear donors always grow slowly and fragile after a series of gene-editing operations. The extracellular matrix (ECM) formulated directly from different organs comprises complex proteins and growth factors that can improve and regulate the cellular functions of primary cells. Herein, sodium lauryl ether sulfate (SLES) detergent was first used to perfuse porcine kidney ECM, and the biological properties of the kidney ECM were optimized. Then, we used a porcine kidney ECM pregel to pattern the microarray and developed a novel strategy to</pubmed_abstract><journal>ACS omega</journal><pubmed_title>Kidney ECM Pregel Nanoarchitectonics for Microarrays to Accelerate Harvesting Gene-Edited Porcine Primary Monoclonal Spheres.</pubmed_title><pmcid>PMC9280780</pmcid><funding_grant_id>2019YFS0138</funding_grant_id><funding_grant_id>2018-CY02-00046-GX</funding_grant_id><funding_grant_id>82070640</funding_grant_id><funding_grant_id>81770618</funding_grant_id><pubmed_authors>Yang G</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Peng W</pubmed_authors><pubmed_authors>Gao M</pubmed_authors><pubmed_authors>He Y</pubmed_authors><pubmed_authors>Bu H</pubmed_authors><pubmed_authors>Bao J</pubmed_authors><pubmed_authors>Wu Q</pubmed_authors><pubmed_authors>Liao G</pubmed_authors><pubmed_authors>Zhu X</pubmed_authors><pubmed_authors>Zhou Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Kidney ECM Pregel Nanoarchitectonics for Microarrays to Accelerate Harvesting Gene-Edited Porcine Primary Monoclonal Spheres.</name><description>One of the key steps of using CRISPR/Cas9 to obtain gene-edited cells used in generating gene-edited animals combined with somatic cell nuclear transplantation (SCNT) is to harvest monoclonal cells with genetic modifications. However, primary cells used as nuclear donors always grow slowly and fragile after a series of gene-editing operations. The extracellular matrix (ECM) formulated directly from different organs comprises complex proteins and growth factors that can improve and regulate the cellular functions of primary cells. Herein, sodium lauryl ether sulfate (SLES) detergent was first used to perfuse porcine kidney ECM, and the biological properties of the kidney ECM were optimized. Then, we used a porcine kidney ECM pregel to pattern the microarray and developed a novel strategy to</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jul</publication><modification>2026-05-09T12:32:53.35Z</modification><creation>2026-04-08T01:00:07.207Z</creation></dates><accession>S-EPMC9280780</accession><cross_references><pubmed>35847249</pubmed><doi>10.1021/acsomega.2c01074</doi></cross_references></HashMap>