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- 规格:
T25
SK-CO-1细胞SK-CO-1细胞系SK-CO-1人结直肠腺癌细胞
Cell line name SK-CO-1
Synonyms SKCO-1; SKCO 1; SKCO1; SKCol1; SK-Col-1; SK Col 1
Accession CVCL_0626
Resource Identification Initiative To cite this cell line use: SK-CO-1 (RRID:CVCL_0626)
Comments Part of: AstraZeneca Colorectal cell line (AZCL) panel.
Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE).
Part of: COSMIC cell lines project.
Part of: KuDOS 95 cell line panel.
Part of: NCI RAS program mutant KRAS cell line panel.
From: Memorial Sloan Kettering Cancer Center; New York; USA.
Registration: Memorial Sloan Kettering Cancer Center Office of Technology Development; SK2010-072.
Population: Caucasian.
Doubling time: 46.56 hours (PubMed=25944804); 46 hours (PubMed=25984343).
Microsatellite instability: Stable (MSS) (PubMed=24755471; PubMed=25926053; Sanger).
Omics: Deep exome analysis.
Omics: Deep proteome analysis.
Omics: Deep quantitative phosphoproteome analysis.
Omics: Deep quantitative proteome analysis.
Omics: DNA methylation analysis.
Omics: shRNA library screening.
Omics: SNP array analysis.
Omics: Transcriptome analysis by microarray.
Omics: Transcriptome analysis by RNAseq.
Derived from site: Metastatic; Ascites; UBERON=UBERON_0007795.
Sequence variations
Mutation; HGNC; HGNC:583; APC; Simple; p.Phe1089fs*37 (c.3266delT); Zygosity=Heterozygous (ATCC=HTB-39; Cosmic-CLP=909718; DepMap=ACH-000400).
Mutation; HGNC; HGNC:583; APC; Simple; p.Pro1443fs*30 (c.4328delC); Zygosity=Heterozygous (ATCC=HTB-39; Cosmic-CLP=909718; DepMap=ACH-000400).
Mutation; HGNC; HGNC:4392; GNAS; Simple; p.Arg201Cys (c.601C>T); ClinVar=VCV000015933; Zygosity=Heterozygous (Cosmic-CLP=909718; DepMap=ACH-000400).
Mutation; HGNC; HGNC:6407; KRAS; Simple; p.Gly12Val (c.35G>T); ClinVar=VCV000012583; Zygosity=Heterozygous (PubMed=12068308; PubMed=20570890; Cosmic-CLP=909718; DepMap=ACH-000400).
Mutation; HGNC; HGNC:11998; TP53; None_reported; -; Zygosity=- (PubMed=16418264).
HLA typing Source: PubMed=26589293
Class I
HLA-A A*01:01,02:01
HLA-B B*35:08,58:05
HLA-C C*05:01,07:01
Genome ancestry Source: PubMed=30894373
Origin % genome
African 0.04
Native American 0.56
East Asian, North 2.24
East Asian, South 0
South Asian 0
European, North 68.7
European, South 28.45
Disease Colon adenocarcinoma (NCIt: C4349)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 65Y
Category Cancer cell line
STR profile Source(s): ATCC=HTB-39; Cosmic-CLP=909718; PubMed=25877200; PubMed=25926053; Technion Genomics Center
Markers:
Amelogenin X (PubMed=25877200)
X,Y (ATCC=HTB-39; Cosmic-CLP=909718; PubMed=25926053; Technion Genomics Center)
CSF1PO 13
D1S1656 13,18.3
D2S441 10,15
D2S1338 17,21
D3S1358 17,18
D5S818 9,11
D7S820 8,10
D8S1179 12,14
D10S1248 13,14
D12S391 18
D13S317 14
D16S539 13
D18S51 19
D19S433 12,13
D21S11 28,30
D22S1045 15
FGA 20,25
Penta D 11
Penta E 13,16
TH01 8,9
TPOX 8,11
vWA 18,19
Run an STR similarity search on this cell line
Web pages
Publications
DOI=10.1007/978-1-4757-1647-4_5
Fogh J., Trempe G.L.
New human tumor cell lines.
(In book chapter) Human tumor cells in vitro; Fogh J. (eds.); pp.115-159; Springer; New York; USA (1975)
PubMed=833871; DOI=10.1093/jnci/58.2.209
Fogh J., Wright W.C., Loveless J.D.
Absence of HeLa cell contamination in 169 cell lines derived from human tumors.
J. Natl. Cancer Inst. 58:209-214(1977)
PubMed=7017212; DOI=10.1093/jnci/66.6.1003
Pollack M.S., Heagney S.D., Livingston P.O., Fogh J.
HLA-A, B, C and DR alloantigen expression on forty-six cultured human tumor cell lines.
J. Natl. Cancer Inst. 66:1003-1012(1981)
PubMed=6220172
Dracopoli N.C., Fogh J.
Polymorphic enzyme analysis of cultured human tumor cell lines.
J. Natl. Cancer Inst. 70:469-476(1983)
PubMed=6582512; DOI=10.1073/pnas.81.2.568; PMCID=PMC344720
Mattes M.J., Cordon-Cardo C., Lewis J.L. Jr., Old L.J., Lloyd K.O.
Cell surface antigens of human ovarian and endometrial carcinoma defined by mouse monoclonal antibodies.
Proc. Natl. Acad. Sci. U.S.A. 81:568-572(1984)
PubMed=3518877; DOI=10.3109/07357908609038260
Fogh J.
Human tumor lines for cancer research.
Cancer Invest. 4:157-184(1986)
PubMed=9294210; DOI=10.1073/pnas.94.19.10330; PMCID=PMC23362
Ilyas M., Tomlinson I.P.M., Rowan A.J., Pignatelli M., Bodmer W.F.
Beta-catenin mutations in cell lines established from human colorectal cancers.
Proc. Natl. Acad. Sci. U.S.A. 94:10330-10334(1997)
PubMed=10737795; DOI=10.1073/pnas.97.7.3352; PMCID=PMC16243
Rowan A.J., Lamlum H., Ilyas M., Wheeler J.M.D., Straub J., Papadopoulou A., Bicknell D.C., Bodmer W.F., Tomlinson I.P.M.
APC mutations in sporadic colorectal tumors: a mutational 'hotspot' and interdependence of the 'two hits'.
Proc. Natl. Acad. Sci. U.S.A. 97:3352-3357(2000)
PubMed=12068308; DOI=10.1038/nature00766
Davies H.R., Bignell G.R., Cox C., Stephens P.J., Edkins S., Clegg S., Teague J.W., Woffendin H., Garnett M.J., Bottomley W., Davis N., Dicks E., Ewing R., Floyd Y., Gray K., Hall S., Hawes R., Hughes J., Kosmidou V., Menzies A., Mould C., Parker A., Stevens C., Watt S., Hooper S., Wilson R., Jayatilake H., Gusterson B.A., Cooper C.S., Shipley J.M., Hargrave D., Pritchard-Jones K., Maitland N.J., Chenevix-Trench G., Riggins G.J., Bigner D.D., Palmieri G., Cossu A., Flanagan A.M., Nicholson A., Ho J.W.C., Leung S.Y., Yuen S.T., Weber B.L., Seigler H.F., Darrow T.L., Paterson H.F., Marais R., Marshall C.J., Wooster R., Stratton M.R., Futreal P.A.
Mutations of the BRAF gene in human cancer.
Nature 417:949-954(2002)
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文献和实验1. Inoculate the entire colony in 5 ml YPD culture O.N. or 12 hours 2. Dilute into YPA medium (1% yeast extract, 2% Bacto-peptone, 2%KOAC) to OD600~ 0.2, Vigorous shaking. 3. For ts mutants, ~15hours at 23C, others ~10 hours at 30C
适用标准:GB/T3536-91(克力夫兰开口杯法)GB/T267-88 产品说明: 本仪器采用当代先进技术,集机械、光学,电子及计算机技术于一体,结构紧凑。可自动完成石油产品开口闪点的测试,实验过程中的升温速率及扫描点火动作由微机控制自动进行,油气闪火时,检测系统自动捕捉并记录闪点温度。对闪点数据进行自动气压修正,并以规范的格式打印输出,还可根据需要重复打印数据。 本仪器可由计算机监控(无线/有线通讯方式,由用户选配)。 本仪器结构合理,性能稳定,操作简单,是理想的分析
刚开始养SK-BR-3时,细胞状态不是很好,贴壁也不均匀,于是开始想办法,考虑是不是吹打的不够,或是传得过多,或是其它的什么,后来发现的确如此,细胞的生长状态与传代的方法有很密切的联系。我的传代方法是:以50平方厘米培养瓶为例,待细胞长满瓶底70%-80%1 、吸除或倒掉瓶内旧培养基。2 、PBS 5ml加入培养瓶,轻轻晃动培养瓶,让PBS流遍细胞表面,倒掉。3 、PBS 5ml加入培养瓶重复洗一次,倒掉。4 、加入1ml胰蛋白酶消化液,轻轻摇动培养瓶,使消化液流遍所有细胞表面,然后置37度
技术资料





