亚洲精品无码成人片久久不卡,亚洲自偷自偷在线传媒,亚洲精品在线,久久无码精品九号,欧洲av人人爽爽,亚洲精品蜜桃久久久久久,亚洲精品久久午夜无码专区电影,辽宁少妇高潮45分钟,少妇高清性色生活片,无码八少妇久久

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 > MeT-5A
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
MeT-5A
MeT-5A
規(guī)格:
貨期:
編號:B165147
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 MeT-5A
商品貨號 B165147
Organism Homo sapiens, human
Tissue mesothelium
Cell Type epithelial virus transformed
Product Format frozen
Morphology epithelial
Culture Properties adherent
Biosafety Level 2 [Cells contain polyomavirus 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.

Disease pleural fluids obtained from non-cancerous individuals.
Applications
The cells can be used to screen chemical and biological agents for activity as growth factor, carcinogens, mutagens, etc.
Storage Conditions liquid nitrogen vapor phase
Disclosure This material is cited in a US or other Patent and may not be used to infringe the claims. Depending on the wishes of the Depositor, ATCC may be required to inform the Patent Depositor of the party to which the material was furnished. This material may not have been produced or characterized by ATCC.
Images Cell micrograph
Derivation

The cells were transfected with the pRSV-T plasmid (an SV40 ori- construct containing the SV40 early region and the Rous sarcoma virus long terminal repeat) and cloned.

Mesothelial cells were isolated from pleural fluids obtained from non-cancerous individuals.

Tumorigenic No
Effects
No, The cells were not tumorigenic in immunosuppressed mice, but did form colonies in semisolid medium.
Comments

The cells stain positively for vimentin, keratins and SV40 T antigen.

Complete Growth Medium The base medium for this cell line is Medium 199 containing 1.5 g/L sodium bicarbonate. 

To make the complete growth medium, add the following components to the base medium: 

10% fetal bovine serum (final conc.)

3.3 nM epidermal growth factor (EGF) (final conc.) (do not filter).
400 nM hydrocortisone (final conc.)
870 nM zinc-free bovine insulin (final conc.)
20 mM HEPES (final conc.)

The trace elements at the following final concentrations:

  • H2SeO3                0.3869 mg/L     (Selenious acid)
  • MnCl2×4H20                     0.0198 mg/L     (Manganese chloride)
  • Na2SiO3×9H20                  14.2100 mg/L  (Sodium silicate)
  • (NH4)6Mo7O24×4H20     0.1236 mg/L     (Ammonium molybdate)
  • NH4VO3                             0.0585 mg/L     (Ammonium vanadate)
  • NiSO4×6H20                     0.0131 mg/L    (Nickle sulfate)
  • SnCl2×2H20                       0.0113 mg/L    (Tin Chloride)
See Methods in Cell Biology, Vol. 21B, pg. 200, 1980

         

This medium is formulated for use with a 5% CO2 in air atmosphere.

ATCC tested fetal bovine serum is available as ATCC Catalog No. 30-2020 (500ml) and ATCC Catalog No. 30-2021 (100ml).

Subculturing Volumes are given for a 75 cm2 flask. Increase or decrease the amount of dissociation medium needed proportionally 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. To remove trypsin-EDTA solution, transfer cell suspension to centrifuge tube and spin at approximately 125 x g for 5 to 10 minutes. Discard supernatant and resuspend cells in fresh growth medium. Add appropriate aliquots of cell suspension to new culture vessels.
  6. Incubate cultures at 37°C.
Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended
Medium Renewal: Every 2 to 3 days
Cryopreservation
Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
Storage temperature: liquid nitrogen vapor phase
Culture Conditions
Temperature: 37°C
STR Profile
Amelogenin: X,Y
CSF1PO: 10,12
D13S317: 11,13
D16S539: 12
D5S818: 12
D7S820: 10
THO1: 6,9.3
TPOX: 8
vWA: 15,18
Name of Depositor The United States of America
References

Reddel RR, et al. Immortalized human bronchial epitherial mesothelial cell lines. US Patent 4,885,238 dated Dec 5 1989

Lechner JF, et al. Asbestos-associated chromosomal changes in human mesothelial cells. Proc. Natl. Acad. Sci. USA 82: 3884-3888, 1985. PubMed: 2987952

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
登封市| 通化县| 陇南市| 璧山县| 成都市| 博湖县| 玉树县| 西乌珠穆沁旗| 北辰区| 眉山市| 东丽区| 诏安县| 光山县| 自贡市| 肇东市| 琼结县| 冀州市| 根河市| 鄂尔多斯市| 名山县| 太仆寺旗| 深泽县| 宁化县| 丽江市| 留坝县| 海原县| 金湖县| 永和县| 乐亭县| 呼玛县| 和平县| 会泽县| 蓬安县| 闸北区| 明溪县| 荣成市| 阳泉市| 新营市| 新乡县| 吉首市| 河源市|