宁波泰斯拓生物

www.testobio.com
  • 本公司产品仅供体外研究使用,不用于临床诊断
首页  /  产品中心  /  进口菌株

产品中心

试剂盒
菌株
质粒
试剂
联系我们  CONTACT US

0574-87917803

testobio@163.com

浙江省宁波市镇海区庄市街道兴庄路9号创e慧谷42号楼B幢401室
最新促销

货号: TS263591

名称: Candida metapsilosis


货号: TS263592

名称: Candida sake


货号: TS131909

名称: HFBCI28


货号: TS131910

名称: Septoria passiflorae Sydow, anamorph


货号: TS131911

名称: Graphium cuneiferum (Berkeley et Broome) Mason et Ellis


货号: TS131912

名称: Streptomyces scabiei (Thaxter) Lambert and Loria


货号: TSTOA0001

名称: Marisediminicola antarctica


货号: TS276951

名称: Real Time PCR EasyTM-Taqman


货号: TS276952

名称: Bacillus subtilis


货号: TS276954

名称: Bacillus subtilis

MeT-5A

货号 TS211477
中文名称 null
适应种属
检测范围
微信小陈 微信小章
在线留言
产品简介
购买须知
产品名称: MeT-5A
商品货号: TS211477
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.xa0

To make the complete growth medium, add the following components to the base medium:xa0

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:

  • H2SeO3xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0 0.3869 mg/Lxa0xa0xa0xa0 (Selenious acid)
  • MnCl2×4H20xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0 0.0198 mg/Lxa0xa0xa0xa0 (Manganese chloride)
  • Na2SiO3×9H20xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0 14.2100 mg/Lxa0 (Sodium silicate)
  • (NH4)6Mo7O24×4H20xa0xa0xa0xa0 0.1236 mg/Lxa0xa0xa0xa0 (Ammonium molybdate)
  • NH4VO3xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0 0.0585 mg/Lxa0xa0xa0xa0 (Ammonium vanadate)
  • NiSO4×6H20xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0 0.0131 mg/L xa0xa0 (Nickle sulfate)
  • SnCl2×2H20xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0xa0 0.0113 mg/L xa0xa0 (Tin Chloride)
See Methods in Cell Biology, Vol. 21B, pg. 200, 1980

xa0xa0xa0xa0xa0xa0xa0xa0xa0

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