亚洲.无码.制服.日韩.中I人妻无码久久精品人妻成人I制片厂91I国产真实91东北熟妇HDXXXI五月AVI四虎精品性爱I国产亚州avI日产精品久久久久I人人爱夜夜操

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(dāng)前位置: 首頁 > ATCC代理 > SNU-449
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
SNU-449
SNU-449
規(guī)格:
貨期:
編號:B165739
品牌:Mingzhoubio

標(biāo)準(zhǔn)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 SNU-449
商品貨號 B165739
Organism Homo sapiens, human
Tissue liver
Product Format frozen
Morphology epithelial; diffusely spreading cells
Culture Properties adherent
Biosafety Level 2  [Cells contain Hepatitis B virus]

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 grade II-III/IV, hepatocellular carcinoma
Age 52 years
Gender male
Ethnicity Asian
Storage Conditions liquid nitrogen vapor phase
Karyotype aneuploid; modal number = 57
Images ATCC CRL-2234 Cell Micrograph
Derivation

SNU-449 was derived in 1990 by J.-G. Park and associates from a primary hepatocellular carcinoma taken from a Korean patient prior to cytotoxic therapy.

Tumor cells were initially cultured in ACL-4 medium supplemented with 5% heat inactivated fetal bovine serum. After establishment, cultures were maintained in RPMI 1640 supplemented with 10% heat-inactivated fetal bovine serum.
Clinical Data
52 years
Asian
male

Comments

Hepatitis B virus (HBV) DNA was detected by Southern blot hybridization. HBV genomic RNA was not expressed.

Grossly, the original tumor was single nodular with perinodular extensions. Histologically, it was predominantly compact and minor trabecular type.

The cultured cells contain a single or double nucleus.

ATCC confirmed this cell line is positive for the presence of Hepatitis B viral DNA sequences.


Complete Growth Medium The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, Catalog No. 30-2001. To make the complete growth medium, add the following components to the base medium: heat-inactivated fetal bovine serum to a final concentration of 10%.
Subculturing Volumes used in this protocol are for 75 cm2 flask; 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 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

Subculture Ratio: 1:5 to 1:10
Medium Renewal: 2 to 3 times a week.
Note: For more information on enzymatic dissociation and subculturing of cell lines consult Chapter 10 in Culture of Animal Cells, a manual of Basic Technique by R. Ian Freshney, 3rd edition, published by Alan R. Liss, N.Y., 1994.

Cryopreservation
Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
Storage temperature: liquid nitrogen vapor phase
Culture Conditions
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Temperature: 37°C
Population Doubling Time 36 hrs
Name of Depositor J Park
Deposited As Homo sapiens
Year of Origin 1990
References

Park JG, et al. Characterization of cell lines established from human hepatocellular carcinoma. Int. J. Cancer 62: 276-282, 1995. PubMed: 7543080

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: 一区二区三区www | 成人影片在线免费观看 | 69国产成人综合久久精品欧美 | 久久久免费少妇 | av片在线观看 | 国产黄色高清 | 天天爱综合 | 亚洲高清视频在线观看免费 | 亚洲涩涩网站 | 日韩理论在线视频 | 99性视频 | 97国产人人 | 丰满少妇一级片 | 久久视频99 | 成人网在线免费视频 | 96久久欧美麻豆网站 | 国产成人精品综合 | 欧美精品久久天天躁 | 国产精品久久久久毛片大屁完整版 | 成人黄色在线看 | av免费播放 | 2020天天干夜夜爽 | 国产成人高清在线 | 亚洲精品综合久久 | 天天射综合 | 国产日韩精品欧美 | 美女网站黄免费 | wwwww.国产 | 久久精品视频网站 | 色综合久久久久综合体 | 天天操天天操 | 国产韩国日本高清视频 | 国产成人一区二区在线观看 | 啪啪动态视频 | 久久精品91久久久久久再现 | 国产小视频免费在线网址 | 久草久草在线 | 成人高清在线观看 | 99热国内精品| 国产女人免费看a级丨片 | 成人av在线直播 | 午夜影院在线观看18 | 青草视频在线 | 久久久久亚洲精品 | 91麻豆产精品久久久久久 | 不卡的av片| 一区二区视频在线免费观看 | av中文电影 | 在线观看视频精品 | 99精品国产视频 | 91精品国产91热久久久做人人 | 悠悠av资源片 | 国产一级免费在线 | 91资源在线 | 精品一二三四五区 | 黄色特级毛片 | 奇米影视8888在线观看大全免费 | 国产精品99久久久久久久久 | 天天操天天爽天天干 | 91污污| 亚洲伊人第一页 | 99视频在线播放 | 五月婷婷.com | 久久手机视频 | 91在线视频导航 | 久草视频在| 91最新视频在线观看 | 日本三级久久 | 国产精品丝袜 | 玖玖在线精品 | 国产一区电影在线观看 | 国产激情电影综合在线看 | 91一区啪爱嗯打偷拍欧美 | 日韩丝袜| 天天操天天舔天天爽 | 97高清免费视频 | 天天色天天干天天 | 精品中文字幕视频 | 色狠狠干 | 蜜桃视频精品 | 狠狠色丁香婷综合久久 | 天堂网一区二区 | 天天插视频 | 91麻豆精品国产91久久久久久 | 日韩亚洲在线视频 | 91av看片 | 在线看黄色的网站 | 亚洲综合视频在线 | 视频二区在线 | 国产精品国产三级国产不产一地 | 色综合久久综合中文综合网 | 亚洲精品视频第一页 | 在线看中文字幕 | 一级α片免费看 | 少妇视频一区 | 麻豆94tv免费版 | 国产精品久久久久久a | 日韩av电影网站在线观看 | 五月天婷婷综合 |