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McA-RH7777
McA-RH7777
規(guī)格:
價(jià)格:
編號(hào):B165104
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
McA-RH7777
商品貨號(hào)
B165104
Organism
Rattus norvegicus, rat
Tissue
liver
培養(yǎng)基
Product Format
frozen
Morphology
epithelial
Culture Properties
loosely 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; Morris hepatoma 7777
Gender
female
Strain
Buffalo
Applications

This cell line is a suitable transfection host.


Storage Conditions
liquid nitrogen vapor phase
Clinical Data
female
Receptor Expression
glucocorticoid
Genes Expressed
alpha-fetoprotein (AFP, alpha fetoprotein)
Cellular Products
alpha-fetoprotein (AFP, alpha fetoprotein)
Comments
Addition of glucocorticoids (dexamethasone) to the medium accelerates cell proliferation and reduces alpha fetoprotein production.
Complete Growth Medium
The base medium for this cell line is ATCC-formulated Dulbecco's Modified Eagle's Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
Subculturing

Heavy monolayer sloughs off; subculture before 70% confluency. 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 culture medium with floating cells to a centrifuge tube. 
  2. If any cells are attached, tap flask gently or if necessary add 2.0 to 3.0 mL of 0.25% Trypsin-0.53 mM EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed. 
  3. Add 2.0 to 3.0 mL of complete growth medium and aspirate cells by gently pipetting. 
  4. To remove trypsin-EDTA solution, transfer cell suspension to the centrifuge tube with the medium and cells from step #1 and spin at approximately 125 x g for 5 to 10 minutes. 
  5. Discard supernatant and resuspend cells in fresh growth medium. Add appropriate aliquots of cell suspension to new culture vessels.
  6. Place culture vessels in incubators at 37°C.
Subcultivation Ratio: A subcultivation ratio of 1:4 to 1:6 weekly is recommended
Medium Renewal: Add medium every 2 to 3 days, do not discard floating cells.
Cryopreservation
Freeze medium: Complete growth medium 95%; DMSO, 5%
Storage temperature: liquid nitrogen vapor phase
Culture Conditions
Temperature: 37°C
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Name of Depositor
JE Becker
Deposited As
Rattus sp.
References

Morris H, Meranze D. Induction and Some Characteristics of “Minimal Deviation” and Other Transplantable Rat Hepatomas. Recent Results Cancer Res. 44: 103-114, 1974.

Kulas DT, et al. The transmembrane protein-tyrosine phosphatase LAR modulates signaling by multiple receptor tyrosine kinases. J. Biol. Chem. 271: 748-754, 1996. PubMed: 8557682

Schock D, et al. An auxiliary factor containing a 240-kDa protein complex is involved in apolipoprotein B RNA editing. Proc. Natl. Acad. Sci. USA 93: 1097-1102, 1996. PubMed: 8577721

Becker JE, et al. Two new rat hepatoma cell lines for studying the unbalanced blocked ontogeny hypothesisIn: Becker JE, et al. Onco-developmental gene expression. New YorkAcademic Press, pp. 259-270, 1976

Cross References

Nucleotide (GenBank) : X56145 Rat mRNA for oncofetal protein (ORF-1A).

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