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IA-XsSBR
IA-XsSBR
規(guī)格:
貨期:
編號:B164821
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 IA-XsSBR
商品貨號 B164821
Organism Rattus norvegicus, rat
Tissue small intestine
Cell Type Epithelial,Epithelial-like
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 adenocarcinoma; radiation (X-ray) induced
Age adult
Gender male
Strain outbred Holtzman
Applications
The IA-XsSBR epithelial-like cell line is a radiation (X-ray) induced small intestine adenocarcinoma derived from an adult male Holtzman rat.
The cells are sensitive to lysis by peripheral blood lymphoid cells from Fischer F344 rats having colon and pancreatic tumors induced by 1,2-dimethylhydrazine or 7,12-dimethylbenz(a)anthracene.
Storage Conditions liquid nitrogen vapor phase
Derivation
The IA-XsSBR epithelial-like cell line is a radiation (X-ray) induced small intestine adenocarcinoma derived from an adult male Holtzman rat. The cells are sensitive to lysis by peripheral blood lymphoid cells from Fischer F344 rats having colon and pancreatic tumors induced by 1,2-dimethylhydrazine or 7,12-dimethylbenz(a)anthracene.
Clinical Data
The IA-XsSBR epithelial-like cell line is a radiation (X-ray) induced small intestine adenocarcinoma derived from an adult male Holtzman rat.
male
Comments
The IA-XsSBR epithelial-like cell line is a radiation (X-ray) induced small intestine adenocarcinoma derived from an adult male Holtzman rat. The cells are sensitive to lysis by peripheral blood lymphoid cells from Fischer F344 rats having colon and pancreatic tumors induced by 1,2-dimethylhydrazine or 7,12-dimethylbenz(a)anthracene.
Complete Growth Medium The base medium for this cell line is ATCC-formulated F-12K Medium, Catalog No. 30-2004. 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 Ca++/Mg++ free Dulbecco's phosphate-buffered saline (D-PBS) or 0.25% (w/v) Trypsin-0.53 mM ) 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: 1:4 to 1:8
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 RH Stevens
Deposited As Rattus sp.
References

Stevens RH, et al. Lymphocyte cytotoxicity in X-irradiation-induced adenocarcinoma of the rat small bowel. I. Measurement of target cell destruction by release of radioiodinated membrane proteins: brief communication. J. Natl. Cancer Inst. 59: 1315-1319, 1977. PubMed: 904002

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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