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MH1C1
MH1C1
規(guī)格:
貨期:
編號(hào):B165151
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 MH1C1
商品貨號(hào) B165151
Organism Rattus norvegicus, rat
Tissue liver
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 hepatoma
Storage Conditions liquid nitrogen vapor phase
Genes Expressed
rat serum albumin; complement components (especially C9)
Cellular Products
rat serum albumin; complement components (especially C9)
Virus Resistance
poliovirus 1
Comments
Cells conjugate and metabolize testosterone and bilirubin.
Complete Growth Medium Hams's F12K medium with 2.0 mM L-glutamine adjusted to contain 1.5 g/L sodium bicarbonate, 82.5%; horse serum, 15%; fetal bovine serum, 2.5%
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- 0.53 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 10 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: A subcultivation ratio of 1:2 to 1:4 is recommended
Medium Renewal: 2 to 3 times per week

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

Name of Depositor AH Tashjian, U Richardson
Deposited As Rattus sp.
References

Richardson UI, et al. Establishment of a clonal strain of hepatoma cells which secrete albumin. J. Cell Biol. 40: 236-247, 1969. PubMed: 4177659

Rommel FA, et al. Synthesis of the ninth component of complement by a clonal strain of rat hepatoma cells. J. Immunol. 105: 396-403, 1970. PubMed: 4194308

Tashjian AH Jr., et al. Multiple differentiated functions in an unusual clonal strain of hepatoma cells. In Vitro 6: 32-45, 1970. PubMed: 4399803

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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