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TGP55
TGP55
規(guī)格:
貨期:
編號(hào):B165857
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 TGP55
商品貨號(hào) B165857
Organism Mus musculus, transgenic, mouse, transgenic
Tissue pancreas
Cell Type Epithelial,Epithelial-like
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.

Disease pancreatic tumor
Age 7.5 months
Gender female
Strain Tg(E1a-1-SV40E)Bri18
Applications
TGP55 is an epithelial-like cell line derived from a pancreatic tumor with small cell anaplastic morphology that arose in an adult female transgenic mouse.
The mouse carried the pseudogene construct composed of elastase-1 promoter linked to the coding region for the SV40 T antigen.
Storage Conditions liquid nitrogen vapor phase
Derivation
TGP55 is an epithelial-like cell line derived from a pancreatic tumor with small cell anaplastic morphology that arose in an adult female transgenic mouse.
Clinical Data
TGP55 is an epithelial-like cell line derived from a pancreatic tumor with small cell anaplastic morphology that arose in an adult female transgenic mouse.
female
Genes Expressed
insulin; somatostatin
Cellular Products
insulin; somatostatin
Comments
TGP55 is an epithelial-like cell line derived from a pancreatic tumor with small cell anaplastic morphology that arose in an adult female transgenic mouse.
The mouse carried the pseudogene construct composed of elastase-1 promoter linked to the coding region for the SV40 T antigen.
The cells do not become confluent.
They grow very slowly as islands, and should be subcultured when the islands begin to form domes.
Complete Growth Medium A 1:1 mixture of Dulbecco's modified Eagle's medium and Ham's F12 medium, 90%; heat-inactivated fetal bovine serum, 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: 1:3 to 1:4
Medium Renewal: Every 4 to 7 days

Note: For more information on enzymatic dissociation and subculturing of cell lines consult Chapter 13 in Culture of Animal Cells, a Manual of Basic Technique by R. Ian Freshney, 5th edition, published by Wiley-Liss, N.Y., 2005.

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 OS Pettengill, D Longnecker
Deposited As mouse, transgenic
References

Pettengill OS, et al. Cell lines derived from pancreatic tumors of Tg(Ela-1-SV40E)Bri18 transgenic mice express somatostatin and T antigen. Carcinogenesis 15: 61-65, 1994. PubMed: 7904904

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.

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