U-2 OS
(ATCC® HTB-96™)
Disease: osteosarcoma
Organism 微生物 Homo sapiens, human
Tissue bone
Product Format 提供形式 frozen
Morphology epithelial Culture Properties adherent
Biosafety Level 生物安全等级 1
Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.
Disease osteosarcoma Age 15 years Gender female Ethnicity Caucasian
Applications This cell line is a suitable transfection host.
Karyotype Cell line U-2 OS is chromosomally highly altered, with chromosome counts in the hypertriploid range.
We did not find the hypodiploid cell population described by J. Ponten, et al., Instead, most of the population has slightly higher counts than first described. Very few normal chromosomes are present, but a high number of stable marker chromosomes are identified., Different chromosomal rearrangements involving the same chromosomes (N1, N7, N9, and N11 particularly), are seen.
Twenty-two markers are found including: t(9qter--->9q21::1p36--->1p::?), 7p+, iso(17q), t(15q;?), 4q+, del(3)(q21), 5q(aberrant) and others. Ref
Images Derivation J. Ponten and E. Saksela derived this line (originally 2T) in 1964 from a moderately differentiated sarcoma of the tibia of a 15 year old girl.
Clinical Data 15 years Caucasian female J. Ponten and E.
Saksela derived this line (originally 2T) in 1964 from a moderately differentiated sarcoma of the tibia of a 15 year old girl.
Antigen Expression Antigen expression: Blood Type A; Rh+; HLA A2, Aw30, B12, Bw35, B40(+/-) Receptor Expression
Receptor expression: insulin-like growth factor I (IGF-I); insulin-like growth factor II (IGF II) Genes
Expressed osteosacoma derived growth factor (ODGF),Blood Type A; Rh+; HLA A2, Aw30, B12, Bw35, B40(+/-)
Comments 注释 Viruses were not detected during co-cultivation with WI-38 cells or in CF tests against SV40, RSV or adenoviruses.
Mycoplasma contamination was detected and eliminated in 1972.
Complete Growth Medium The base medium for this cell line is ATCC-formulated McCoy's 5a Medium Modified, Catalog No. 30-2007.
To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
Subculturing Remove medium, and rinse with 0.25% trypsin, 0.03% EDTA solution.
Remove the solution and add an additional 1 to 2 mL of trypsin-EDTA solution.
Allow the flask to sit at room temperature (or at 37℃) until the cells detach.
Add fresh culture medium, aspirate and dispense into new culture flasks.
Corning® T-75 flasks (catalog #430641) are recommended for subculturing this product.
Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:6 is recommended Medium Renewal: 2 to 3 times per week Cryopreservation Culture medium, 95%; DMSO, 5%
Culture Conditions 培养条件
Temperature 培养温度 : 37℃
STR Profile Amelogenin: X CSF1PO: 13 D13S317: 13 D16S539: 11,12 D5S818: 11 D7S820: 11,12 THO1: 6,9.3 TPOX: 11,12 vWA: 14,18 Isoenzymes AK-1, 1 ES-D, 1 G6PD, B GLO-I, 2 PGM1, 2 PGM3, 1
Name of Depositor Hellstrom Year of Origin 1964
References 参考文献 Heldin CH, et al. A human osteosarcoma cell line secretes a growth factor structurally related to a homodimer of PDGF A-chains. Nature 319: 511-514, 1986. PubMed: 3456080
Ponten J, Saksela E. Two established in vitro cell lines from human mesenchymal tumours. Int. J. Cancer 2: 434-447, 1967. PubMed: 6081590
Raile K, et al. Human osteosarcoma (U-2 OS) cells express both insulin-like growth factor-I (IGF-I) receptors and insulin-like growth factor-II/mannose-6- phosphate (IGF-II/M6P) receptors and synthesize IGF-II: autocrine growth stimulation by IGF-II via the IGF-I receptor. J. Cell. Physiol. 159 : 531-541 , 1994. PubMed: 8188767
Landers JE, et al. Translational enhancement of mdm2 oncogene expression in human tumor cells containing a stabilized wild-type p53 protein. Cancer Res. 57: 3562-3568, 1997. PubMed: 9270029
Moradpour D, et al. Characterization of cell lines allowing titghtly regulated expression of heapatitis C virus core protein. Virology 222: 51-63, 1996. PubMed: 8806487
Ponten J, Saksela E. Two established in vitro cell lines from human mesenchymal tumours. Int. J. Cancer 2: 434-447, 1967. PubMed: 6081590
微生物菌种资源
1、用户在微生物菌种查询网订购时请仔细确认订单后再下单,因菌株特殊性由用户选择而造成的退货需求,我单位不予受理(特殊情况除外)。
2、用户在收到菌株后请立即核验菌株包裹,若发现任何包装规格、数量、名称不符,外观破损,损毁等问题请在3个工作日内反馈给我单位业务人员并会及时处理上述问题。
3、用户收到快递包裹后,如果有漏发或发错货的情况,请在用户签收包裹之日起3个工作日内,将破损或发错的货品、加盖公章的换货申请表、邮运公司人员在场的开箱视频以及出库清单复印件一起寄给我们,可以顺丰到付。我们将在收到后,尽快核实并予以处理。
4、因微生物菌株属于活的生物制品如冻干常温运输4°C冰箱保存2-20年;如斜面培养物则用户收到后尽快实验。如西林瓶请置于-20°C可以保藏5-10年。如甘油管请置于-80°C并定期转接以确保其活性。
5、提交订单,一定要写菌株的编号,如不写,视为认可提供的该属种的任意菌株;提供的菌株,均只提供菌株打管说明或者菌株证明于网站下载;美国ATCC菌株绝大多数有COA;特声明告知,如再因以上情况引起异议与反悔,概不退菌。
6、已经确认退货的话用户需把运单号及时告知,且与我单位客服联系退款换货事宜。
细胞系原代细胞株
1、用户在中国微生物菌种查询网订购时请仔细确认订单后再下单,因细胞特殊性由用户选择而造成的退货需求,我单位不予受理(特殊情况除外)。
2、细胞运输途中遭遇的各种问题,细胞丢失、瓶身破损、培养液严重漏液等,重发;细胞污染问题,请在收到产品24小时内,给我们提出真实的实验结果,核实后重发等。
3、其他因细胞引起的需要重发补发可以参考单位网站《细胞售后服务告知书》栏目。
4、已经确认退货的话用户需把运单号及时告知,且与我单位客服联系退款或者换货事宜。
其他产品
1、用户在中国微生物菌种查询网订购时请仔细确认订单后再下单,因产品特殊性由用户选择而造成的退货需求,我单位不予受理(特殊情况除外)。
2、产品在运输途中遭遇的各种问题,产品丢失、瓶身破损、漏液等,均可申请退换货。
3、用户收到快递包裹后,如果有漏发或发错货的情况,请在用户签收包裹之日起3个工作日内,将破损或发错的货品、加盖公章的换货申请表、邮运公司人员在场的开箱视频以及出库清单复印件一起寄给我们,可以顺丰到付。我们将在收到后,尽快核实并予以处理。
4、已经确认退货的话用户需把运单号及时告知,且与我单位客服联系退款换货事宜。
固定电话:010-53515223
业务手机:18610886853,18610241664,18701099593,18971386853,18701098095
微信号码:vrmte521(18610886853企业微信);18610241664;biobw0905(18701098095)
企业公众号:800185668
官方邮箱:biobw11@sina.com(微生物菌种查询网)
投诉电话:biobw8888(18701099593)