人妻少妇偷人精品无码丨色婷婷av久久久久久久丨欧美xxxx做受性欧美88丨欧洲女人牲交视频免费丨亚洲精品久久久av无码专区

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 > 127TAg
最近瀏覽歷史
聯系我們
  • 0574-87157013
  • mingzhoubio@163.com
  • 浙江省寧波市鎮海區莊市街道興莊路9號
  • 創e慧谷42號樓B幢401室
127TAg
127TAg
規格:
貨期:
編號:B162656
品牌:Mingzhoubio

標準菌株
定量菌液
DNA
RNA

規格:
凍干粉
斜面
甘油
平板


產品名稱 127TAg
商品貨號 B162656
Organism Mus musculus, mouse
Tissue embryo
Cell Type fibroblast immortalized with SV40 large T antigenSV40 large T antigen transfected
Product Format frozen
Morphology fibroblast
Culture Properties adherent
Biosafety Level 2 cells containing SV40 viral DNA sequences

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.

Age 14.5 days gestation embryo
Applications
DNA repair studies
Storage Conditions liquid nitrogen vapor phase
Images
Derivation
127TAg (Pms2 null [-/-]) is a mouse embryonic fibroblast (MEF) cell line derived from Pms-2 null embryos at day 14.5 of gestation. The Pms-2 deficient mice were constructed using ES-D3 [D3] embryonic stem cells [PubMed: 9096356]. The cell line was established by transfection with an expression vector for SV40 large T antigen [PubMed: 8538772]. The cells are transgenic for lambda LIZ (Lac I/cII).
Comments
127TAg (Pms2 null [-/-]) is a mouse embryonic fibroblast (MEF) cell line derived from Pms-2 null embryos at day 14.5 of gestation. The Pms-2 deficient mice were constructed using ES-D3 [D3] embryonic stem cells [PubMed: 9096356]. The cell line was established by transfection with an expression vector for SV40 large T antigen [PubMed: 8538772]. The cells are transgenic for lambda LIZ (Lac I/cII).
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
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.
    An inoculum of 3 X 10(3) to 1 X 10(4) viable cells/cm2 is recommended.
  6. Incubate cultures at 37°C.
Interval: Maintain cultures at a cell concentration between 3 X 10(3) and 1 X 10(4) cells/cm2.
Subcultivation Ratio: A subcultivation ratio of 1:6 to 1:8 is recommended
Medium Renewal: Every two to three days
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: 37.0°C
Population Doubling Time 17 hours
Name of Depositor RW Sobol
Year of Origin 2000
References

Sobol RW, et al. Requirement of mammalian DNA polymerase-beta in base-excision repair. Nature 379: 183-186, 1996. PubMed: 8538772

Sobol RW, et al. Base excision repair intermediates induce p53-independent cytotoxic and genotoxic responses. J. Biol. Chem. 278: 39951-39959, 2003. PubMed: 12882965

Narayanan L, et al. Elevated levels of mutation in multiple tissues of mice deficient in the DNA mismatch repair gene Pms2. Proc. Natl. Acad. Sci. USA 94: 122-127, 1997. PubMed: 9096356

Sobol RW, et al. Mutations associated with base excision repair deficiency and methylation-induced genotoxic stress. Proc. Natl. Acad. Sci. USA 99: 6860-6865, 2002. PubMed: 11983862

Sobol RW, et al. The lyase activity of the DNA repair protein beta-polymerase protects from DNA-damage-induced cytotoxicity. Nature 405: 807-810, 2000. PubMed: 10866204

梅經理 17280875617 1438578920
胡經理 13345964880 2438244627
周經理 17757487661 1296385441
于經理 18067160830 2088210172
沈經理 19548299266 2662369050
李經理 13626845108 972239479
主站蜘蛛池模板: 无码国产成人久久| 亚洲欧美日韩成人综合一区| 亚洲综合熟女久久久40p| 成人网站免费高清视频在线观看| 国产99爱在线视频免费观看| 男人j进入女人j内部免费网站| 非洲人与性动交ccoo| 337p西西人体大胆瓣开下部| 亚洲国产精品一区二区动图| 亚洲1卡二卡三新区2022| 狠狠躁18三区二区一区ai明星 | 98视频精品全部国产| 国产精品_九九99久久精品| 久久精品超碰av无码| 女人被强╳到高潮喷水在线观看| 国产免国产免费| 高清性欧美暴力猛交| 亚洲 小说 欧美 另类 社区| 精品卡一卡二卡3卡高清乱码| 国产l精品国产亚洲区久久| 动漫人妻h无码中文字幕| 宅宅午夜无码一区二区三区| 久久精品无码一区二区三区免费| 国产亚洲一区二区在线观看| 四虎国产精亚洲一区久久特色| 性色av一区二区三区人妻| 四虎成人精品无码| 最新中文字幕av无码专区| 99热国产这里只有精品9| 国产成人免费高清直播| 无码乱码av天堂一区二区| 红杏亚洲影院一区二区三区| 亚洲aⅴ永久无码一区二区三区| 最大胆裸体人体牲交免费| 国产二级一片内射视频插放 | 国产亚洲婷婷香蕉久久精品| 亚洲综合一区无码精品| 国产日产欧产精品精品app| 四虎成人国产精品永久在线| аⅴ资源中文在线天堂| 插鸡网站在线播放免费观看|