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首頁>細(xì)胞CELL>biobw自建細(xì)胞系>人骨髓瘤細(xì)胞MM1.S
人骨髓瘤細(xì)胞MM1.S
    人骨髓瘤細(xì)胞MM1.S
  • 平臺編號:bio-129535
  • 細(xì)胞信息: MM1S
  • 規(guī)格:1×10?cells/T25培養(yǎng)瓶
  • 用途:細(xì)胞系
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  • 注意事項(xiàng):僅用于科學(xué)研究或者工業(yè)應(yīng)用等非醫(yī)療目的不可用于人類或動物的臨床診斷或治療,非藥用,非食用(產(chǎn)品信息以出庫為準(zhǔn))

  細(xì)胞名稱:人骨髓瘤細(xì)胞MM1.S

  產(chǎn)品規(guī)格:T25培養(yǎng)瓶x1;1.5ml凍存管x2

  細(xì)胞數(shù)量:1x10^6;1x10^6

  保存溫度:37℃;-198℃

  運(yùn)輸方式:常溫保溫運(yùn)輸;干冰運(yùn)輸

  安全等級:1

  用途限制:僅供科研2類

  培養(yǎng)體系:DMEM高糖+10%FBS+1%三抗

  培養(yǎng)溫度:37℃

  二氧化碳濃度:5%

  簡介:人骨髓瘤細(xì)胞MM1.S取自45歲女性供體外周血。該細(xì)胞源于ATCC

  注釋:Part of:Cancer Cell Line Encyclopedia(CCLE)project.

  Part of:COSMIC cell lines project.

  Part of:MD Anderson Cell Lines Project.

  Characteristics:Produces IgA lambda.

  Characteristics:Sensitive to dexamethasone.

  Doubling time:80 hours(PubMed=25984343).

  Microsatellite instability:Instable(MSI-low)(Sanger).

  Omics:Array-based CGH.

  Omics:Deep exome analysis.

  Omics:Deep RNAseq analysis.

  Omics:DNA methylation analysis.

  Omics:Protein expression by reverse-phase protein arrays.

  Omics:shRNA library screening.

  Omics:SNP array analysis.

  Omics:Transcriptome analysis.

  Derived from sampling site:Peripheral blood.

  基因突變:Heterozygous for KRAS p.Gly12Ala(c.35G>C)(PubMed=21173094;CCLE;Cosmic-CLP).

  Homozygous for TRAF3 p.Val536_Asn545delValPheValAlaGlnThrValLeuGluAsninsAsp(c.1604-1630delTCTTTGTGGCCCAAACTGTTCTAGAAA)(PubMed=17692805).

  HLA信息:/

  STR信息

  Amelogenin X

  CSF1PO 9,14

  D3S1358 16,17

  D5S818 8,12

  D7S820 10,11

  D8S1179 14

  D13S317 13

  D16S539 12

  D18S51 11,16

  D21S11 29,30

  FGA 20,24

  Penta D 2.2,9

  Penta E 13,15

  TH01 7,8

  TPOX 8

  vWA 15,17

  參考文獻(xiàn)

  PubMed=30285677;DOI=10.1186/s12885-018-4840-5

  Tan K.-T.,Ding L.-W.,Sun Q.-Y.,Lao Z.-T.,Chien W.,Ren X.,Xiao J.-F.,Loh X.-Y.,Xu L.,Lill M.,Mayakonda A.,Lin D.-C.,Yang H.,Koeffler H.P.

  Profiling the B/T cell receptor repertoire of lymphocyte derived cell lines.

  BMC Cancer 18:940-940(2018)

  PubMed=30545397;DOI=10.1186/s13045-018-0679-0

  Tessoulin B.,Moreau-Aubry A.,Descamps G.,Gomez-Bougie P.,Maiga S.,Gaignard A.,Chiron D.,Menoret E.,Le Gouill S.,Moreau P.,Amiot M.,Pellat-Deceunynck C.

  Whole-exon sequencing of human myeloma cell lines shows mutations related to myeloma patients at relapse with major hits in the DNA regulation and repair pathways.

  J.Hematol.Oncol.11:137-137(2018)

  PubMed=30894373;DOI=10.1158/0008-5472.CAN-18-2747

  Dutil J.,Chen Z.,Monteiro A.N.,Teer J.K.,Eschrich S.A.

  An interactive resource to probe genetic diversity and estimated ancestry in cancer cell lines.

  Cancer Res.79:1263-1273(2019)

  PubMed=31068700;DOI=10.1038/s41586-019-1186-3

  Ghandi M.,Huang F.W.,Jane-Valbuena J.,Kryukov G.V.,Lo C.C.,McDonald E.R.III,Barretina J.,Gelfand E.T.,Bielski C.M.,Li H.,Hu K.,Andreev-Drakhlin A.Y.,Kim J.,Hess J.M.,Haas B.J.,Aguet F.,Weir B.A.,Rothberg M.V.,Paolella B.R.,Lawrence M.S.,Akbani R.,Lu Y.,Tiv H.L.,Gokhale P.C.,de Weck A.,Mansour A.A.,Oh C.,Shih J.,Hadi K.,Rosen Y.,Bistline J.,Venkatesan K.,Reddy A.,Sonkin D.,Liu M.,Lehar J.,Korn J.M.,Porter D.A.,Jones M.D.,Golji J.,Caponigro G.,Taylor J.E.,Dunning C.M.,Creech A.L.,Warren A.C.,McFarland J.M.,Zamanighomi M.,Kauffmann A.,Stransky N.,Imielinski M.,Maruvka Y.E.,Cherniack A.D.,Tsherniak A.,Vazquez F.,Jaffe J.D.,Lane A.A.,Weinstock D.M.,Johannessen C.M.,Morrissey M.P.,Stegmeier F.,Schlegel R.,Hahn W.C.,Getz G.,Mills G.B.,Boehm J.S.,Golub T.R.,Garraway L.A.,Sellers W.R.

  Next-generation characterization of the Cancer Cell Line Encyclopedia.

  Nature 569:503-508(2019)

  細(xì)胞操作說明書下載:細(xì)胞操作說明書

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