MDS-L cell line is a blastic subline originated from MDS92 which was established from the bone marrow of a patient with MDS. MDS-L cells proliferate in the presence of IL-3 and have lost maturing capacity unlike the parental MDS92. MDS-L is a parental cell line of MDS-L-2007 and MDS-LGF.
1) TheRECIPIENT of BIOLOGICAL RESOURCE shall obtain a priorcon sent on use of it from the DEVELOPER and DEPOSITOR. The RECIPIENT shall conclude a MTA with the depositor. 2) In publishing the research results obtained by use of the BIOLOGICAL RESOURCE, a citation of the following literature (Leukemia 2018 32(8):1846-1850) designated by the DEPOSITOR is requested. 3) In publishing the research results to be obtained by use of the BIOLOGICAL RESOURCE, an acknowledgment to the DEPOSITOR is requested.
Kawasaki University of Medical Welfare Industry-Academia Collaboration and Intellectual Property Management Section 577 Matsushima, Kurashiki-city, Okayama 701-0192 JAPAN E-mail. s-renkei@med.kawasaki-m.ac.jp
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splice donor site mutation of TP53 (c.672+1G>A; homozygous; COSM6906) NRAS (G12A) mutation (heterozygous; COSM565) CEBPA (Q311stop) mutation (heterozygous; COSM29221) HIST1H3C (K27M) mutation (heterozygous; COSM1580151) in a part of the cells
細胞寿命
infinite
細胞形態
lymphocyte-like
分化機能特性
Whole cells retain immature blastic features and differentiation-induction is successful at present.
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