波多野结衣毛片-乳色吐息在线观看-国产伦子伦对白视频-性做久久久-狠狠干2019-黄色裸体片-美女无遮挡免费网站-国产91熟女高潮一区二区-懂色av蜜臀av粉嫩av分享-小h片在线观看-台湾佬在线-日韩激情在线播放-欧日韩不卡在线视频-波多野结衣中文字幕一区-天天操夜夜草

熱門搜索:A549    293T 金黃色葡萄球菌 大腸桿菌 AKK菌
購物車 1 種商品 - 共0元
當前位置: 首頁 > ATCC代理 > NM2C5
最近瀏覽歷史
聯(lián)系我們
  • 0574-87157013
  • mingzhoubio@163.com
  • 浙江省寧波市鎮(zhèn)海區(qū)莊市街道興莊路9號
  • 創(chuàng)e慧谷42號樓B幢401室
NM2C5
NM2C5
規(guī)格:
貨期:
編號:B225120
品牌:Mingzhoubio

標準菌株
定量菌液
DNA
RNA

規(guī)格:
凍干粉
斜面
甘油
平板


產(chǎn)品名稱 NM2C5
商品貨號 B225120
Organism Homo sapiens, human
Cell Type melanocyte, Melanoma
Product Format frozen
Morphology epithelial
Culture Properties adherent
Biosafety Level 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 cancer
Age 31 years
Gender female
Ethnicity Caucasian
Applications These well characterized, tumorigenic human isogenic cell lines have dramatically opposite metastatic phenotypes and are ideal for metastatic studies.
Storage Conditions liquid nitrogen vapor phase
Images
Derivation

The parental cell lines ATCC CRL-2918 (NM2C5) and ATCC CRL-2914 ?(M4A4) were derived from the human breast cancer cell line, MDA-MB-435.

Note: Recent studies have generated questions about the origin of the parent cell line, MDA-MB-435. Additional studies have since corroborated a melanocyte origin of MDA-MB-435, to which ATCC has responded by pursuing its own investigation into the identity of this cell line.

The NM2C5 GFP (ATCC CRL-2919) cell line was developed by the transduction of the GFP gene into NM2C5 (ATCC CRL-2918) cell line.

Clinical Data
31 years
Caucasian
female
Antigen Expression
CD44; Homo sapiens, expressed
Receptor Expression
epidermal growth factor (EGF), expressed
Oncogene c-myc; Ras; p53
Comments
Note: Recent studies have generated questions about the origin of the parent cell line, MDA-MB-435. Additional studies have since corroborated a melanocyte origin of MDA-MB-435, to which ATCC has responded by pursuing its own investigation into the identity of this cell line.

M4A4 is highly metastatic in immuno-deprived mice, while NM2C5 is weakly or virtually non-metastatic.

Gene expression analysis of the cells produced microarrays in which MDA-MB-435 clustered with cell lines of melanoma origin instead of breast.

The cell line to which MDA-MB-435 is reported to have been cross-contaminated with is the M14 melanoma line RefRae JM, et al. Common origins of MDA-MB-435 cells from various sources with those shown to have melanoma properties. Clin. Exp. Metastasis 21: 543-552, 2004. PubMed: 15679052 RefRoss DT, et al. Systematic variation in gene expression patterns in human cancer cell lines. Nature Genetics 24: 227-235, 2000. PubMed: 10700174 RefEllison G, et al. Further evidence to support the melanocytic origin of MDA-MB-435. Mol. Pathol. 55: 294-299, 2002. PubMed: 12354931. RefSellappan S, et al. Lineage infidelity of MDA-MB-435 cells: expression of melanocyte proteins in a breast cancer cell line. Cancer Res. 64: 3479-3485, 2004. PubMed: 15150101. RefRae JM, et al., MDA-MB-435 cells are derived from M14 Melanoma cells - a loss for breast cancer, but a boon for melanoma research. Breast Cancer Res. Treat. 104:13-19, 2007. PubMed: 17004106.

Complete Growth Medium The base medium for this cell line is ATCC-formulated Dulbecco's Modified Eagle's Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
Subculturing
To avoid phenotypic drift it is recommended to make frozen aliquots of the cells and use each aliquot for only 10 passages.

Volumes used in this protocol are for 75 sq cm flasks; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes.
  1. Remove and discard culture medium.
  2. Briefly rinse the cell layer with Ca++/Mg++ free Dulbecco's phosphate-buffered saline (D-PBS) or 0.25% (w/v) Trypsin - 0.53 mM EDTA solution to remove all traces of serum which contains trypsin inhibitor.
  3. Add 1.0 to 2.0 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. Transfer cell suspension to a centrifuge tube and spin at approximately 125 x g for 5 to 10 minutes. Discard supernatant.
  6. Resuspend the cell pellet in fresh growth medium. Add appropriate aliquots of the cell suspension to new culture vessels. An inoculum of 4 x 103 to 7 x 103 viable cells/cm2 is recommended.
  7. Incubate cultures at 37°C. We recommend that you maintain cultures at a cell concentration between 9 x 104 and 1.5 x 105 cells/cm2.
Subcultivation Ratio: A subcultivation ratio of 1:8 to 1:12 is recommended
Medium Renewal: 2 to 3 times a week
Note: For more information on enzymatic dissociation and subculturing of cell lines consult Chapter 13 in Culture Of Animal Cells: A Manual Of Basic Technique by R. Ian Freshney, 5th edition, published by Wiley-Liss, N.Y., 2005.
Cryopreservation
Complete growth medium, 95%; DMSO, 5%. Cell culture tested DMSO is available as ATCC? Catalog No. 4-X.

Culture Conditions
Temperature: 37°C
Atmosphere: 5% CO2 in air recommended
STR Profile
Amelogenin: X
CSF1PO: 11
D13S317: 12
D16S539: 13
D5S818: 11,12
D7S820: 8,10
THO1: 6,7
TPOX: 8,11
vWA: 16,18
Population Doubling Time about 31 hours
Name of Depositor D Tarin
Year of Origin 1992
References

Ross DT, et al. Systematic variation in gene expression patterns in human cancer cell lines. Nature Genetics 24: 227-235, 2000. PubMed: 10700174

Bao L, et al. Correlation of VLA-4 integrin expression with metastatic potential in various human tumour cell lines. Differentiation 52: 239-246, 1993. PubMed: 7683291

Urquidi V, et al. Contrasting expression of thrombospondin-1 and osteopontin correlates with absence or presence of metastatic phenotype in an isogenic model of spontaneous human breast cancer metastasis. Clin. Cancer Res. 8: 61-74, 2003. PubMed: 11801541

Rae JM, et al. Common origins of MDA-MB-435 cells from various sources with those shown to have melanoma properties. Clin. Exp. Metastasis 21: 543-552, 2004. PubMed: 15679052

Goodison S, et al. Prolonged dormancy and site-specific growth potential of cancer cells spontaneously disseminated from nonmetastatic breast tumors as revealed by labeling with green fluorescent protein. Clin. Cancer Res. 9: 3808-3814, 2003. PubMed: 14506175

Montel V, et al. Expression profiling of primary tumors and matched lymphatic and lung metastases in a xenogeneic breast cancer model. Am. J. Pathol. 166: 1565-1579, 2005. PubMed: 15855655

Suzuki M, et al. Dormant cancer cells retrieved from metastasis-free organs regain tumorigenic and metastatic potency. Am. J. Pathol. 169: 673-681, 2006. PubMed: 16877365

Montel V, et al. Tumor-stromal interactions reciprocally modulate gene expression patterns during carcinogenesis and metastasis. Int. J. Cancer 119: 251-263, 2006. PubMed: 16482564

Goodison S, et al. Molecular cytogenetic analysis of a human breast metastasis model: identification of phenotype-specific chromosomal rearrangements. Cancer Genet. Cytogenet. 156: 37-48, 2005. PubMed: 15588854

Hayashi K, et al. Differential effects of retinoic acid on the growth of isogenic metastatic and non-metastatic breast cancer cell lines and their association with distinct expression of retinoic acid receptor beta isoforms 2 and 4. Int. J. Oncol. 22: 623-629, 2003. PubMed: 12579317

Tarin DTumor metastasisIn: Tarin DOxford Textbook of PathologyOxford, United KingdomOxford University Press607-663, 1992

Sellappan S, et al. Lineage infidelity of MDA-MB-435 cells: expression of melanocyte proteins in a breast cancer cell line. Cancer Res. 64: 3479-3485, 2004. PubMed: 15150101.

Ellison G, et al. Further evidence to support the melanocytic origin of MDA-MB-435. Mol. Pathol. 55: 294-299, 2002. PubMed: 12354931.

Rae JM, et al., MDA-MB-435 cells are derived from M14 Melanoma cells - a loss for breast cancer, but a boon for melanoma research. Breast Cancer Res. Treat. 104:13-19, 2007. PubMed: 17004106.

Hay, R. J., Caputo, J. L., and Macy, M. L., Eds. (1992), ATCC Quality Control Methods for Cell Lines. 2nd edition, Published by ATCC.

Caputo, J. L., Biosafety procedures in cell culture. J. Tissue Culture Methods 11:223-227, 1988.

Fleming, D.O., Richardson, J. H., Tulis, J.J. and Vesley, D., (1995) Laboratory Safety: Principles and Practice. Second edition, ASM press, Washington, DC.

梅經(jīng)理 17280875617 1438578920
胡經(jīng)理 13345964880 2438244627
周經(jīng)理 17757487661 1296385441
于經(jīng)理 18067160830 2088210172
沈經(jīng)理 19548299266 2662369050
李經(jīng)理 13626845108 972239479
主站蜘蛛池模板: 97xxx| 色婷婷麻豆 | 在线观看你懂得 | wwww欧美| 私人影院毛片 | 欧美xxxxxx片免费播放软件 | 成人有色视频 | 狗爬女子的视频 | 无码国产精品高潮久久99 | 欧美三级免费观看 | 爽妇网国产精品 | 亚洲第一自拍 | 久久久久久久久久av | 色av综合网 | 国产91在线看 | 97精品一区二区视频在线观看 | 99精品网站 | www.99爱| 超碰69| 福利国产片 | 成人免费网站在线观看 | 国产在线一级 | 欧美色图首页 | 在线观看成人免费 | 久久成人毛片 | 香蕉视频一区二区三区 | 亚洲 欧美 激情 小说 另类 | 97精品一区二区视频在线观看 | 日本不卡在线观看 | 色.www | 日韩欧美视频在线免费观看 | 色中文字幕在线观看 | 九九热精品视频 | 国产精品呻吟久久 | 精品黑人一区二区三区观看时间 | 久久尤物| 亚洲天堂精品视频 | 伊人精品一区二区三区 | 天堂av√| 国产精品不卡在线 | 久久性av| 中文字幕第一页在线播放 | 玉足脚交榨精h文 | 色综合久 | 伊人69 | 女人夜夜春 | 色吧视频 | 天天激情综合 | 中国黄色录像 | 黄色a级片在线观看 | 欧洲美一区二区三区亚洲 | 亚洲看片网站 | 男生和女生靠逼视频 | 超碰2020| 99国产精品一区二区三区 | 污视频网站在线看 | 成人av在线网站 | 欧美xxxx视频 | 国产免费看 | 福利视频一区 | 免费黄色大片 | 人妻熟女一区二区三区app下载 | 日韩三级一区二区三区 | 丰满人妻老熟妇伦人精品 | 中文字幕免费在线播放 | 日韩午夜毛片 | 日韩在线网 | 成人娱乐网 | 隣の若妻さん波多野结衣 | 国产经典一区二区 | 国产精品久久久久久久久久久久午夜片 | 激情小说图片视频 | 亚洲少妇网 | 国产精品视频久久久久久 | 国产日韩欧美在线播放 | 亚洲最大成人网站 | 国产午夜精品福利视频 | 午夜激情久久 | 男人的天堂影院 | 国产一区亚洲 | 国产一区二区麻豆 | 欧美日韩亚洲国产一区 | 亚洲精品国产成人av在线 | 欧美日韩国产三区 | 欧美第一页草草影院 | 久久久一级片 | 欧美国产一区二区 | 麻豆精品一区 | 2019亚洲天堂| 亚洲第八页 | 久久综合五月天 | 亚洲一区和二区 | 亚洲经典一区二区三区 | 性感少妇av | 日本久热 | 亚洲大片在线观看 | 热久久91 | 亚洲国产中文字幕 | 无码免费一区二区三区 |