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NK92/NK92/NK92/人恶性非霍奇金淋巴瘤患者的自然

杀伤细胞
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  • 2025年07月25日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 英文名

      NK92

    • 库存

      1x10^6/瓶/支

    • 供应商

      上海酶研

    • 肿瘤类型

      详询

    • 细胞类型

      人恶性非霍奇金淋巴瘤患者的自然杀伤细胞

    • ATCC Number

      详询

    • 品系

      NK92

    • 组织来源

      人恶性非霍奇金淋巴瘤患者的自然杀伤细胞

    • 相关疾病

      NK92

    • 物种来源

      哺乳动物

    • 免疫类型

      详询

    • 细胞形态

      贴壁/悬浮

    • 是否是肿瘤细胞

      详询

    • 器官来源

      人恶性非霍奇金淋巴瘤患者的自然杀伤细胞

    • 运输方式

      顺丰快递

    • 年限

      5年

    • 生长状态

      生长良好

    NK92/NK92细胞系/NK92细胞株/NK92人恶性非霍奇金淋巴瘤患者的自然杀伤细胞

    Cell line name NK-92

    Synonyms NK92; Natural Killer-92; NK-92.05; Neukoplast; aNK

    Accession CVCL_2142

    Resource Identification Initiative To cite this cell line use: NK-92 (RRID:CVCL_2142)

    Comments Group: Patented cell line.

    Part of: LL-100 blood cancer cell line panel.

    Registration: International Depositary Authority, American Type Culture Collection (ATCC); PTA-6670.

    Population: Caucasian.

    Characteristics: Laboratory use as a standard cell line for antibody-dependent cell-mediated cytotoxicity (ADCC) testing. Also being developed for cellular adoptive immunotherapy for cancers and viral infections.

    Characteristics: IL2 dependent.

    Characteristics: Does not express FCGR3A/CD16.

    Doubling time: 35.6 +- 6.1 hours (PubMed=31126350); ~40-50 hours (DSMZ=ACC-488).

    Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).

    Omics: Deep exome analysis.

    Omics: Transcriptome analysis by microarray.

    Omics: Transcriptome analysis by RNAseq.

    Miscellaneous: Neukoplast is used as a trademark to refer to NK-92 cells that are available for non-human research applications while aNK is used as a trademark to refer to cells from the cGMP-grade NK-92 cell-line that is in use for therapeutic human testing.

    Caution: This cell line is exclusively owned and controlled by NantKwest, Inc. NantKwest and its affiliate, Brink Biologics, Inc. are the sole authorized distributors for both commercial and non-commercial research requestors. There are no other authorized commercial and noncommercial suppliers of NK-92 cells. Contact NantKwest and Brink Biologics for information concerning current inventory and cell line use and support.

    Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.

    Cell type: Natural killer cell; CL=CL_0000623.

    DOI=10.1016/B978-0-12-221970-2.50457-5

    Drexler H.G.

    The leukemia-lymphoma cell line factsbook.

    (In book) ISBN 9780122219702; pp.1-733; Academic Press; London; United Kingdom (2001)

     

    PubMed=11454312; DOI=10.1089/152581601750288975

    Maki G., Klingemann H.-G., Martinson J.A., Tam Y.K.

    Factors regulating the cytotoxic activity of the human natural killer cell line, NK-92.

    J. Hematother. Stem Cell Res. 10:369-383(2001)

     

    PubMed=12850795; DOI=10.1080/14653240310001523

    Tam Y.K., Martinson J.A., Doligosa K., Klingemann H.-G.

    Ex vivo expansion of the highly cytotoxic human natural killer-92 cell-line under current good manufacturing practice conditions for clinical adoptive cellular immunotherapy.

    Cytotherapy 5:259-272(2003)

     

    PubMed=16827800; DOI=10.1111/j.1349-7006.2006.00226.x; PMCID=PMC11159954

    Liu A., Takakuwa T., Luo W.-J., Fujita S., Aozasa K.

    Alterations in ATR in nasal NK/T-cell lymphoma and chronic active Epstein-Barr virus infection.

    Cancer Sci. 97:605-610(2006)

     

    PubMed=18424763; DOI=10.4049/jimmunol.180.9.6392; PMCID=PMC2810560

    Binyamin L., Alpaugh R.K., Hughes T.L., Lutz C.T., Campbell K.S., Weiner L.M.

    Blocking NK cell inhibitory self-recognition promotes antibody-dependent cellular cytotoxicity in a model of anti-lymphoma therapy.

    J. Immunol. 180:6392-6401(2008)

     

    PubMed=19194464; DOI=10.1038/leu.2009.3

    Iqbal J., Kucuk C., Deleeuw R.J., Srivastava G., Tam W., Geng H., Klinkebiel D.L., Christman J.K., Patel K., Cao K., Shen L., Dybkaer K., Tsui I.F.L., Ali H.H., Shimizu N., Au W.Y., Lam W.L., Chan W.-C.

    Genomic analyses reveal global functional alterations that promote tumor growth and novel tumor suppressor genes in natural killer-cell malignancies.

    Leukemia 23:1139-1151(2009)

     

    PubMed=20454443; DOI=10.1155/2010/904767; PMCID=PMC2861168

    Uphoff C.C., Denkmann S.A., Steube K.G., Drexler H.G.

    Detection of EBV, HBV, HCV, HIV-1, HTLV-I and -II, and SMRV in human and other primate cell lines.

    J. Biomed. Biotechnol. 2010:904767.1-904767.23(2010)

     

    PubMed=21052088; DOI=10.1038/leu.2010.255

    Iqbal J., Weisenburger D.D., Chowdhury A., Tsai M.-Y., Srivastava G., Greiner T.C., Kucuk C., Deffenbacher K.E., Vose J.M., Smith L., Au W.Y., Nakamura S., Seto M., Delabie J., Berger F., Loong F., Ko Y.-H., Sng I., Liu X., Loughran T.P. Jr., Armitage J.O., Chan W.-C.

    International Peripheral T-cell Lymphoma Project

    Natural killer cell lymphoma shares strikingly similar molecular features with a group of non-hepatosplenic gammadelta T-cell lymphoma and is highly sensitive to a novel aurora kinase A inhibitor in vitro.

    Leukemia 25:348-358(2011)

     

    PubMed=21570725; DOI=10.1016/j.molimm.2011.04.010

    Schnueriger A., Grau R., Sondermann P., Schreitmueller T., Marti S., Zocher M.

    Development of a quantitative, cell-line based assay to measure ADCC activity mediated by therapeutic antibodies.

    Mol. Immunol. 48:1512-1517(2011)

     

    PubMed=25586472; DOI=10.1038/ncomms7025; PMCID=PMC7743911

    Kucuk C., Jiang B., Hu X.-Z., Zhang W.-Y., Chan J.K.C., Xiao W.-M., Lack N., Alkan C., Williams J.C., Avery K.N., Kavak P., Scuto A., Sen E., Gaulard P., Staudt L.M., Iqbal J., Zhang W.-W., Cornish A., Gong Q., Yang Q.-P., Sun H., d'Amore F.A., Leppa S., Liu W.-P., Fu K., de Leval L., McKeithan T.W., Chan W.-C.

    Activating mutations of STAT5B and STAT3 in lymphomas derived from gammadelta-T or NK cells.

    Nat. Commun. 6:6025.1-6025.12(2015)

     

    PubMed=26559813; DOI=10.1007/s00262-015-1761-x; PMCID=PMC11029582

    Suck G., Odendahl M., Nowakowska P., Seidl C., Wels W.S., Klingemann H.-G., Tonn T.

    NK-92: an 'off-the-shelf therapeutic' for adoptive natural killer cell-based cancer immunotherapy.

    Cancer Immunol. Immunother. 65:485-492(2016)

     

    PubMed=30054012; DOI=10.1016/j.molimm.2018.07.015; PMCID=PMC6345623

    Gunesch J.T., Angelo L.S., Mahapatra S., Deering R.P., Kowalko J.E., Sleiman P., Tobias J.W., Monaco-Shawver L., Orange J.S., Mace E.M.

    Genome-wide analyses and functional profiling of human NK cell lines.

    Mol. Immunol. 115:64-75(2019)

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    *发表【中文论文】请标注:由上海酶研生物科技有限公司提供;

    *发表【英文论文】请标注:From Shanghai EK-Bioscience Biotechnology Co., Ltd.

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      GNHu20  人  恶性非霍奇金淋巴瘤患者自然杀伤细胞,   1000元 NK-92MI  GNHu22  人  恶性非霍奇金淋巴瘤患者自然杀伤细胞,  1000元NRK  GNR 2  大鼠  肾细胞  400元 OK  GNO20  负鼠  负鼠肾细胞  1000元 OS-RC-2  TCHu 40  人  肾癌细胞  450元 P19  TCM27  小鼠  睾丸畸胎瘤细胞  1000元 P3/NSI/1-Ag4-1 [NS-1]  TCM25  小鼠  骨髓瘤细胞  400元 P

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