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FAT 7
FAT 7
規格:
價格:
編號:B164437
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
FAT 7
商品貨號
B164437
Organism
Rattus norvegicus, rat
Tissue
nasal
培養基
Product Format
frozen
Morphology
epithelial
Culture Properties
adherent
Biosafety Level
1

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
squamous cell carcinoma
Age
adult
Gender
male
Applications
The FAT 7 line was established from a nasal squamous cell carcinoma induced by formaldehyde inhalation in an adult male rat.
The cells contain a point mutation in the conserved V region of the p53 gene at codon 271 (CGT --> CAT transversion).
Storage Conditions
liquid nitrogen vapor phase
Derivation
The FAT 7 line was established from a nasal squamous cell carcinoma induced by formaldehyde inhalation in an adult male rat.
Clinical Data
The FAT 7 line was established from a nasal squamous cell carcinoma induced by formaldehyde inhalation in an adult male rat.
male
Receptor Expression
epidermal growth factor (EGF)
Genes Expressed
transforming growth factor alpha (TGF alpha)
Cellular Products
transforming growth factor alpha (TGF alpha)
Tumorigenic
Yes
Effects
Yes, in female CD-1 nude mice
Comments
The FAT 7 line was established from a nasal squamous cell carcinoma induced by formaldehyde inhalation in an adult male rat.
The cells contain a point mutation in the conserved V region of the p53 gene at codon 271 (CGT --> CAT transversion).
Complete Growth Medium
Ham's F12K medium with 0.01 mg/ml insulin, 250 ng/ml hydrocortisone and 0.0025 mg/ml transferrin, 90%; 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: 1:5 to 1:10
Medium Renewal: Every 2 to 3 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%
Population Doubling Time
24 hrs
Name of Depositor
E Bermudez
Deposited As
Rattus sp.
References

Bermudez E, et al. Characterization of cell lines derived from formaldehyde-induced nasal tumors in rats. Mol. Carcinog. 9: 193-199, 1994. PubMed: 8148052

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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