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        1. 上海復(fù)祥生物科技有限公司

          人卵巢癌細(xì)胞

          參   考   價(jià): ¥ 1

          訂  貨  量: ≥1 件

          具體成交價(jià)以合同協(xié)議為準(zhǔn)

          產(chǎn)品型號(hào):SK-OV-3

          品       牌:其他品牌

          廠商性質(zhì):生產(chǎn)商

          所  在  地:上海市

          更新時(shí)間:2024-11-12 21:02:08瀏覽次數(shù):2028

          聯(lián)系我時(shí),請(qǐng)告知來(lái)自 化工儀器網(wǎng)
          供貨周期 一周 規(guī)格 T25
          貨號(hào) SK-OV-3 應(yīng)用領(lǐng)域 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥
          主要用途 普通細(xì)胞株 - 科研實(shí)驗(yàn)
          HTB-77 SK-OV-3 人卵巢癌細(xì)胞,
          ATCC 細(xì)胞|細(xì)胞系|細(xì)胞株|腫瘤細(xì)胞|細(xì)胞,細(xì)胞庫(kù)管理規(guī)范,
          提供的細(xì)胞株背景清楚,提供參考文獻(xiàn)和培養(yǎng)條件

          HTB-77 SK-OV-3 人卵巢癌細(xì)胞

          ATCC® Number: HTB-77™ Price: $272.00

          Designations: SK-OV-3 [SKOV-3]

          Depositors: G Trempe, LJ Old

          Biosafety Level: 1

          Shipped: frozen

          Medium & Serum: See Propagation

          Growth Properties: adherent

          Organism: Homo sapiens (human)

          Morphology: epithelial

          HTB-77 SK-OV-3 人卵巢癌細(xì)胞

          Source: Organ: ovary

          Disease: adenocarcinoma

          Derived from metastatic site: ascites

          Permits/Forms: In addition to the MTA mentioned above, other ATCC and/or regulatory permits may be required for the transfer of this ATCC material. Anyone purchasing ATCC material is ultimay responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.


          Restrictions: The cells are distributed for research purposes only. The Memorial Sloan-Kettering Cancer Center releases the line subject to the following: 1.) The cells or their products must not be distributed to third parties. Commercial interests are the exclusive property of Memorial Sloan-Kettering Cancer Center. 2.) Any proposed commercial use of these cells must first be negotiated with The Director, Office of Industrial Affairs, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021; phone (212) 639-6181; (212) 717-3439.

          Isolation: Isolation date: 1973

          Applications: transfection host (Nucleofection technology from Lonza

          Roche FuGENE® Transfection Reagents)

          Tumorigenic: Yes

          Antigen Expression: Blood Type B; Rh+

          DNA Profile (STR): Amelogenin: X

          CSF1PO: 11

          D13S317: 8,11

          D16S539: 12

          D5S818: 11

          D7S820: 13,14

          THO1: 9,9.3

          TPOX: 8,11

          vWA: 17,18

          Cytogenetic Analysis: This is a hypodiploid human cell line. The modal chromosome number was 43, occurring in 63.3% of cells. The range was 42 to 45. The rate of higher ploidies was 32%. The del(1)(q21), der(13)t(1;?;13) (q11;?;q34), der(11)t(11;?) (q12), del(10)(q22) and 3 other marker chromosomes were common to most cells, and 3 others were found only in some cells. One N11 had the HSR segment from p11 to the distal end. The normal N10, N12, N15, N17 and N19 were absent. Others were either single or paired. There were from 1 to 6 rearranged and unassignable chromosomes. The X chromosome was either single or paired.

          Isoenzymes: AK-1, 1

          ES-D, 1

          G6PD, B

          GLO-I, 1-2

          Me-2, 1

          PGM1, 1-2

          PGM3, 1

          Age: 64 years

          Gender: female

          Ethnicity: Caucasian

          Comments: SK-OV-3 cells are resistant to tumor necrosis factor and to several cytotoxic drugs including diphtheria toxin, cis-platinum and adriamycin.

          Propagation: ATCC 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%.

          Atmosphere: air, 95%; carbon dioxide (CO2), 5%

          Temperature: 37.0°C

          Subculturing: Protocol:

          1.Remove and discard culture medium.

          2.Briefly rinse the cell layer with 0.25% (w/v) Trypsin- 0.53 mM EDTA solution to remove all traces of serum that contains trypsin inhibitor.

          3.Add 2.0 to 3.0 ml of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).

          Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37°C to facilitate dispersal.

          4.Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting.

          5.Add appropriate aliquots of the cell suspension to new culture vessels.

          6.Incubate cultures at 37°C.

          Subc*tion Ratio: A subc*tion ratio of 1:2 to 1:6 is recommended

          Medium Renewal: 2 to 3 times per week

          Preservation: Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO

          Storage temperature: liquid nitrogen vapor phase

          Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2007

          recommended serum:ATCC 30-2020

          References: 21869: . Human tumor cells in vitro. New York: Plenum Press; 1975.

          22536: Fogh J, et al. Absence of HeLa cell contamination in 169 cell lines derived from human tumors. J. Natl. Cancer Inst. 58: 209-214, 1977. PubMed: 833871

          22539: Fogh J, et al. One hundred and twenty-seven cultured human tumor cell lines producing tumors in nude mice. J. Natl. Cancer Inst. 59: 221-226, 1977. PubMed: 327080

          23103: Morimoto H, et al. Overcoming tumor necrosis factor and drug resistance of human tumor cell lines by combination treatment with anti-Fas antibody and drugs or toxins. Cancer Res. 53: 2591-2596, 1993. PubMed: 7684321

          23478: Morimoto H, et al. Synergistic effect of tumor necrosis factor-alpha- and diphtheria toxin- mediated cytotoxicity in sensitive and resistant human ovarian tumor cell lines. J. Immunol. 147: 2609-2616, 1991. PubMed: 1918981

          32281: Zhang X, et al. Microfilament depletion and circumvention of multiple drug resistance by sphinxolides. Cancer Res. 57: 3751-3758, 1997. PubMed: 9288783

          32456: Clinton GM, et al. Estrogens increase the expression of fibulin-1, an extracellular matrix protein secreted by human ovarian cancer cells. Proc. Natl. Acad. Sci. USA 93: 316-320, 1996. PubMed: 8552629

          32530: Zhang X, Smith CD. Microtubule effects of welwistatin, a cyanobacterial indolinone that circumvents multiple drug resistance. Mol. Pharmacol. 49: 288-294, 1996. PubMed: 8632761

          90272: Wiechen K, et al. Suppression of the c-erbB-2 gene product decreases transformation abilities but not the proliferation and secretion of proteases of SK-OV-3 ovarian cancer cells. Br. J. Cancer 81: 790-795, 1999. PubMed: 10555747

          90273: Yu D, et al. Enhanced c-erbB-2/neu expression in human ovarian cancer cells correlates with more severe malignancy that can be suppressed by E1A. Cancer Res. 53: 891-898, 1993. PubMed: 8094034

          90274: Karlan BY, et al. Glucocorticoids stabilize HER-2/neu messenger RNA in human epithelial ovarian carcinoma cells. Gyn. Onc. 53: 70-77, 1994. PubMed: 7909787



          HTB-77 SK-OV-3




















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