Cell No. : Cell Name
RCB3555 : ATL-35T(-)
update : 2024/10/02
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Comment | BSL2. Currently not ready. We don't know whether virus particles are produced or not. Therefore, the cells must be handled under BSL2. |
Comment from the depositor | Non-leukemic cell line (IL-2 independent). |
Terms and conditions | |
Remarks | |
Order Form |
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Regarding MTA between user institutions and RIKEN BRC, there are two kinds of MTA, not-for-profit academic purpose (C-XXXX) and for-profit research purpose (C-XXXXp) , depending on the sort of user institutions and the purposes of use. Please use an appropriate MTA(to see). In relation to commercial use and use for patent filing, first of all Please contact RIKEN BRC (cellbank.brc@riken.jp).
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Basic information
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Expected time |
Upon a request we will start preparation. Contact us: cellkitaku.brc@riken.jp
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BSL |
BSL2
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Cellosaurus(Expasy) |
CVCL_8339
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Reference information |
Reference |
4
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User's Publication |
0
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Reference |
3175
Michiyuki Maeda, Junko Tanabe-Shibuya, Paola Miyazato, Hiroshi Masutani, Jun-Ichirou Yasunaga, Kazumasa Usami, Akira Shimizu, Masao Matsuoka
IL-2/IL-2 Receptor Pathway Plays a Crucial Role in the Growth and Malignant Transformation of HTLV-1-Infected T Cells to Develop Adult T-Cell Leukemia
Front Microbiol
2020
11:356
PubMed ID: 32210945
DOI: 10.3389/fmicb.2020.00356
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2505
Ahsan MK, Masutani H, Yamaguchi Y, Kim YC, Nosaka K, Matsuoka M, Nishinaka Y, Maeda M, Yodoi J.
Loss of interleukin-2-dependency in HTLV-I-infected T cells on gene silencing of thioredoxin-binding protein-2
Oncogene
2006
25(15):2181-91
PubMed ID: 16314839
DOI: 10.1038/sj.onc.1209256
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2761
K Nosaka, M Maeda, S Tamiya, T Sakai, H Mitsuya, M Matsuoka
Increasing methylation of the CDKN2A gene is associated with the progression of adult T-cell leukemia
Cancer Res
2000
60(4):1043-8
PubMed ID: 10706122
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2510
Maeda M, Noma T, Hama K, Honjo T.
Application of a human T cell line derived from a Sézary syndrome patient for human interleukin 4 assay
Immunol Lett
1988
18(4):247-53
PubMed ID: 3263317
DOI: 10.1016/0165-2478(88)90170-8
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