【ATCC来源】C3H/10T1/2, Clone 8、C3
H/10T1/2, Clone 8、C3H/10T1/2, Clone 8细胞、C3H/10T1/2, Clone 8细胞、C3H/10T1/2, Clone 8C3H/10T1/2, Clone 8[小鼠胚胎成纤维细胞]- ￥1400
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- 详细信息
- 文献和实验
- 技术资料
- 英文名：
C3H/10T1/2, Clone 8
- 库存：
1x10^6/cell
- 供应商：
上海酶研
- 肿瘤类型：
无
- 细胞类型：
C3H/10T1/2, Clone 8
- ATCC Number：
详询
- 品系：
C3H/10T1/2, Clone 8
- 组织来源：
C3H/10T1/2, Clone 8[小鼠胚胎成纤维细胞]
- 相关疾病：
//
- 物种来源：
小鼠
- 免疫类型：
1
- 细胞形态：
正常
- 是否是肿瘤细胞：
否
- 器官来源：
C3H/10T1/2, Clone 8[小鼠胚胎成纤维细胞]
- 运输方式：
自取或顺丰快递发货
- 年限：
永久
- 生长状态：
活力好，代次低
- 规格：
瓶
【ATCC来源】C3H/10T1/2, Clone 8、C3H/10T1/2, Clone 8、C3H/10T1/2, Clone 8细胞、C3H/10T1/2, Clone 8细胞、C3H/10T1/2, Clone 8C3H/10T1/2, Clone 8[小鼠胚胎成纤维细胞]
Cell line name C3H/10T1/2 clone 8
Synonyms C3H/10T1/2-clone8; C3H/10T1/2 CL8; C3H10T1/2 clone8; C3H10T1/2CL8; 10T1/2(clone8); 10T1/2; C3H10T1-2; C3H10T1/2; C3H-10T1/2; C3H 10T1/2; C3H/10T1/2
Accession CVCL_0190
Resource Identification Initiative To cite this cell line use: C3H/10T1/2 clone 8 (RRID:CVCL_0190)
Comments Group: Space-flown cell line (cellonaut).
Part of: ENCODE project mouse cell lines.
Doubling time: 15.5 hours (Note=At 9th passage) (PubMed=4357355).
Omics: SNP array analysis.
Misspelling: C3HIOT 1/2; NCI-DTP=C3HIOT 1/2.
Misspelling: C3HT101/2; Note=Occasionally.
Derived from site: In situ; Whole embryo; UBERON=UBERON_0000922.
Cell type: Fibroblast; CL=CL_0000057.
Species of origin Mus musculus (Mouse) (NCBI Taxonomy: 10090)
Breed/subspecies: C3H.
Hierarchy Children:
CVCL_0117 (30A-5) CVCL_HA77 (7SA) CVCL_C4L8 (C3H10T1/2 MRF4-#7)
CVCL_C4L9 (C3H10T1/2 MyoD1-#8) CVCL_C4LA (C3H10T1/2 myogenin-#1) CVCL_5I32 (C3H/10T1/2-mRuby clone 2)
CVCL_4720 (C3H/MCA clone 15) CVCL_4721 (C3H/MCA clone 16) CVCL_Y467 (C3H/MCA-58)
CVCL_C5IW (C3RL4)
Sex of cell Sex unspecified
Age at sampling Embryo
Category Spontaneously immortalized cell line
Publications
PubMed=4357355
Reznikoff C.A., Brankow D.W., Heidelberger C.
Establishment and characterization of a cloned line of C3H mouse embryo cells sensitive to postconfluence inhibition of division.
Cancer Res. 33:3231-3238(1973)
PubMed=4796800
Reznikoff C.A., Bertram J.S., Brankow D.W., Heidelberger C.
Quantitative and qualitative studies of chemical transformation of cloned C3H mouse embryo cells sensitive to postconfluence inhibition of cell division.
Cancer Res. 33:3239-3249(1973)
PubMed=3152871; DOI=10.1007/BF01128016
Christie N.T., Sen P., Costa M.
Chromosomal alterations in cell lines derived from mouse rhabdomyosarcomas induced by crystalline nickel sulfide.
Biol. Met. 1:43-50(1988)
PubMed=25277546; DOI=10.1186/1471-2164-15-847; PMCID=PMC4198738
Didion J.P., Buus R.J., Naghashfar Z., Threadgill D.W., Morse H.C. 3rd, Pardo-Manuel de Villena F.
SNP array profiling of mouse cell lines identifies their strains of origin and reveals cross-contamination and widespread aneuploidy.
BMC Genomics 15:847.1-847.11(2014)
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文献和实验*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.
a look from the following website just by clicking "Tyrosine Phosphorylation and Dimerization" http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WSN-43F85YV-2&_user=1111158&_coverDate=06%2F29%2F2001&_rdoc=1&_fmt=full&_orig=search
扫描仪中，都采用机械式的二维X，Y线性扫描技术实现，即X，Y方向都采用直线驱动器和直线导轨实现往复运动。此类装置，由于驱动系统的频率限制，驱动器的扫描惯性大，使得扫描效率低，分析时间相当长；并且往复行程长，对直线导轨的精度要求相当高。二、光机结合的二维扫描系统为同样实现生物芯片的二维扫描，我们的实验装置设计如图2，采用了振镜和大数值孔径的远心f-è物镜相结合实现X方向扫描，Y方向的运动仍采用直线驱动器和直线导轨实现。 系统中，对于f-è物镜，满足x＝2fè（è为振镜的摆动角度，f为物镜焦距）的线性
Analysis of RB Action in DNA Damage Checkpoint Response
checkpoint response: (1) transcriptional repression of E2F-regulated genes (cyclin A reporter assay); (2) induction of cell cycle arrest (Brd-U incorporation assay); and (3) inhibition of DNA double-strand break accumulation (phosphorylated-histone H2A.X
技术资料