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 > As4.1
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
As4.1
As4.1
規(guī)格:
貨期:
編號:B163959
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 As4.1
商品貨號 B163959
Organism Mus musculus, mouse
Tissue kidney
Product Format frozen
Morphology epithelial
Culture Properties adherent
Biosafety Level 2  [Cells contain papovavirus]

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.

Gender female
Applications
transfection host
Storage Conditions liquid nitrogen vapor phase
Derivation
As4.1 was established from the ascites fluid of a six month old transgenic mouse harboring an intraparenchymal kidney tumor induced by transgene targeted tumorigenesis.
These transgenic mice were constructed with the renin T antigen fusion gene, pR2d4.6TAG which contains a transcriptional fusion between Ren-2d 5' flanking sequences and the structural gene for SV40 T antigen.
Clinical Data
female
Genes Expressed
renin
Cellular Products
renin
Comments The cell line was cloned by picking a small cluster from a dish seeded at low density.
The As4.1 cells express high levels of correctly processed renin mRNA from the endogenous Ren-1c locus.
They constitutively secrete prorenin and appear to store a proteolytically cleaved form of active renin intracellularly in storage granules/vesicles.
It has been reported that each As4.1 cell contains 1000 to 2000 copies of renin mRNA.
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 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-0.53mM EDTA solution to remove all traces of serum which 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.

Subcultivation Ratio: 1:6 to 1:12
Medium Renewal: Every 2 to 3 days

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

Complete growth medium described above supplemented with 5% (v/v) DMSO.  Cell culture tested DMSO is available as ATCC Catalog No. 4-X.

Culture Conditions
Temperature: 37°C
Atmosphere: Air, 95%; Carbon dioxide (CO2), 5%
Name of Depositor KW Gross
Deposited As Mus musculus
References

Jones CA, et al. Expression of murine renin genes during fetal development. Mol. Endocrinol. 4: 375-383, 1990. PubMed: 2188116

Sigmund CD, et al. Tissue and cell specific expression of a renin promoter-reporter gene construct in transgenic mice. Biochem. Biophys. Res. Commun. 170: 344-350, 1990. PubMed: 1695507

Sigmund CD, et al. Isolation and characterization of renin-expressing cell lines from transgenic mice containing a renin-promoter viral oncogene fusion construct. J. Biol. Chem. 265: 19916-19922, 1990. PubMed: 2174057

Petrovic N, et al. Role of proximal promoter elements in regulation of renin gene transcription. J. Biol. Chem. 271: 22499-22505, 1996. PubMed: 8798416

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.

Biosafety in Microbiological and Biomedical Laboratories, 5th ed. HHS. U.S. Department of Health and Human Services, Centers for Disease Control and Prevention. Washington DC: U.S. Government Printing Office; 2007. The entire text is available online.

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: 日99久9在线 | 免费| 日韩新无码精品毛片| 亚洲婷婷开心色四房播播| 伊人色综合一区二区三区影院视频| 国产精品久久国产精品99 | 狠狠做五月深爱婷婷| 国产一精品一av一免费| 熟妇人妻无码中文字幕老熟妇| 国产精品国产三级国产an| 亚洲精品成人网站在线| 久久久久黑人强伦姧人妻| 男女啪啪做爰高潮免费网站| 日韩国产网曝欧美第一页| 国产黑色丝袜在线看片不卡顿| 国产精品夜色一区二区三区| 美女裸体无遮挡免费视频网站 | 久久中文精品无码中文字幕| 亚洲日韩精品无码专区加勒比海| 日韩精品人成在线播放| 人人妻人人妻人人片av| 国产在线拍揄自揄视频网试看| 亚洲精品一区二区三区影院| 乱色精品无码一区二区国产盗| 亚洲一二三四2021不卡| 在线看片免费人成视频在线影院| 亚洲综合色88综合天堂| 俺去俺来也在线www色官网| 久久久久人妻一区二区三区vr| 日本护士xxxxhd少妇| 国产精品久久久久久久久久红粉 | 秋霞午夜久久午夜精品| 精品国产乱码久久久软件下载| 无码毛片aaa在线| 99久久久无码国产精品秋霞网| 自拍偷亚洲产在线观看| 欧美情侣性视频| 欧美xxxx黑人又粗又长精品| 天天躁夜夜躁狠狠躁2020| 亚洲欧美成人精品香蕉网| 欧美成人看片黄a免费看| 中文字幕丰满伦子无码|