| 產(chǎn)品名稱 |
MA-104 Clone 1 |
| 商品貨號 |
B165058 |
| Organism |
Cercopithecus aethiops |
| Tissue |
kidney |
| Cell Type |
epithelial |
| 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. |
| Age |
embryo |
| Applications |
This cell line is a suitable transfection host. |
| Storage Conditions |
liquid nitrogen vapor phase |
| Derivation |
An African green monkey pure cell population was isolated at the ATCC by cloning MA-104. MA-104 was developed by initial explant culture and subsequent passage by enzymatic dissociation at Microbiological Associates from embryonic Rhesus monkey kidney tissue. |
| Virus Susceptibility |
Simian rotavirus
|
| Comments |
This item is not available for international distribution. |
| Complete Growth Medium |
The base medium for this cell line is ATCC-formulated Eagle's Minimum Essential Medium, Catalog No. 30-2003. 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.
- Remove and discard culture medium.
- 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.
- 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.
- Add 6.0 to 8.0 mL of complete growth medium and aspirate cells by gently pipetting.
- Add appropriate aliquots of the cell suspension to new culture vessels.
An inoculum of 5 x 103 to 7 x 103 viable cells/cm2 is recommended.
- Incubate cultures at 37°C
Subculture Ratio: 1:3 to 1:10
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 |
Freeze medium: Complete growth medium, 95%; DMSO, 5% Storage temperature: liquid nitrogen vapor phase |
| Population Doubling Time |
27 hours |
| Name of Depositor |
MM Vincent |
| Year of Origin |
2001 |
| References |
Whitaker AM, Hayward CJ. The characterization of three monkey kidney cell lines. Dev. Biol. Stand. 60: 125-131, 1985. PubMed: 4043530
MA-104 was developed by initial explant culture and subsequent passage by enzymatic dissociation at Microbiological Associates from embryonic Rhesus monkey kidney tissue. Chromosome and isoenzyme analysis of the cells distributed by some sources showed that the species of origin was African green monkey (PubMed: 4043530). In May of 1994, M.M. Vincent deposited ampules of MA-104 at passage 3 at the ATCC. At passage 16 and higher, presence of both African green monkey and Rhesus monkey cells were detected by isoenzyme analysis. An African green monkey pure cell population was isolated at the ATCC by cloning MA-104. (ATCC CRL-2378). This line is available as MA-104 clone 1 (CRL-2378.1).
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