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首頁>細(xì)胞CELL>biobw自建細(xì)胞系>人黑色素瘤細(xì)胞系M14
人黑色素瘤細(xì)胞系M14
    人黑色素瘤細(xì)胞系M14
  • 平臺編號:bio-73228
  • 細(xì)胞信息: M14
  • 規(guī)格:1×10?cells/T25培養(yǎng)瓶
  • 用途:/
  • 服務(wù)費用:
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  • 注意事項: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:人黑色素瘤細(xì)胞系M14

  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℃

  運輸方式:常溫保溫運輸;干冰運輸

  安全等級:1

  用途限制:僅供科研2類

  培養(yǎng)體系:90%DMEM+10%FBS+1%三抗

  培養(yǎng)溫度:37℃

  二氧化碳濃度:5%

  簡介:人黑色素瘤細(xì)胞系M14取自33歲男性供體。貼壁培養(yǎng)。

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

  Part of:COSMIC cell lines project.

  Part of:MD Anderson Cell Lines Project.

  Part of:NCI-60 cancer cell line panel.

  Doubling time:26.3 hours(NCI-DTP).

  Microsatellite instability:Stable(MSS)(Sanger).

  Omics:Array-based CGH.

  Omics:CNV analysis.

  Omics:Deep exome analysis.

  Omics:Deep proteome analysis.

  Omics:DNA methylation analysis.

  Omics:Fluorescence phenotype profiling.

  Omics:lncRNA expression profiling.

  Omics:Metabolome analysis.

  Omics:Protein expression by reverse-phase protein arrays.

  Omics:SNP array analysis.

  Omics:Transcriptome analysis.

  基因突變

  Heterozygous for BRAF p.Val600Glu(c.1799T>A)(ClinVar=VCV000013961)(PubMed=12068308;PubMed=17088437;PubMed=19799798;PubMed=29492214).

  Heterozygous for CDKN2A c.150+2T>C(IVS1+2T>C);splice donor mutation and c.455insCdel26(PubMed=19799798;PubMed=29492214).

  Heterozygous for TP53 p.Gly266Glu(c.797G>A)(ClinVar=VCV000161516)(PubMed=17088437;PubMed=18277095).

  HLA信息

  Class I

  HLA-A A*11:01:01,24:02:01

  HLA-B B*15,35

  HLA-C C*03:03:01,04

  Class II

  HLA-DP DPB1*13:01,19:01

  HLA-DQ DQB1*03:02,06:03

  HLA-DR DRB1*04:05:01,13:01:01

  STR信息

  Amelogenin X

  CSF1PO 11

  D1S1656 11,12

  D2S441 11,14

  D2S1338 19,24

  D3S1358 14,16

  D5S818 11,12

  D7S820 8,10

  D8S1179 13

  D10S1248 14

  D12S391 18,19

  D13S317 12

  D16S539 9,13

  D18S51 13,17

  D19S433 14,15

  D21S11 30

  D22S1045 15

  FGA 21

  SE33 15,22

  TH01 6,7

  TPOX 8,11

  vWA 16,18

  參考文獻

  PubMed=27807467;DOI=10.1186/s13100-016-0078-4

  Zampella J.G.,Rodic N.,Yang W.R.,Huang C.R.L.,Welch J.,Gnanakkan V.P.,Cornish T.C.,Boeke J.D.,Burns K.H.

  A map of mobile DNA insertions in the NCI-60 human cancer cell panel.

  Mob.DNA 7:20-20(2016)

  PubMed=28196595;DOI=10.1016/j.ccell.2017.01.005

  Li J.,Zhao W.,Akbani R.,Liu W.,Ju Z.,Ling S.,Vellano C.P.,Roebuck P.,Yu Q.,Eterovic A.K.,Byers L.A.,Davies M.A.,Deng W.,Gopal Y.N.V.,Chen G.,von Euw E.M.,Slamon D.J.,Conklin D.,Heymach J.V.,Gazdar A.F.,Minna J.D.,Myers J.N.,Lu Y.,Mills G.B.,Liang H.

  Characterization of human cancer cell lines by reverse-phase protein arrays.

  Cancer Cell 31:225-239(2017)

  PubMed=28940260;DOI=10.1002/ijc.31067

  Korch C.,Hall E.M.,Dirks W.G.,Ewing M.,Faries M.,Varella-Garcia M.,Robinson S.,Storts D.R.,Turner J.A.,Wang Y.,Burnett E.C.,Healy L.,Kniss D.,Neve R.M.,Nims R.W.,Reid Y.A.,Robinson W.A.,Capes-Davis A.

  Authentication of M14 melanoma cell line proves misidentification of MDA-MB-435 breast cancer cell line.

  Int.J.Cancer 142:561-572(2017)

  PubMed=29492214;DOI=10.18632/oncotarget.23989

  Sini M.C.,Doneddu V.,Paliogiannis P.,Casula M.,Colombino M.,Manca A.,Botti G.,Ascierto P.A.,Lissia A.,Cossu A.,Palmieri G.

  Genetic alterations in main candidate genes during melanoma progression.

  Oncotarget 9:8531-8541(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)


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