產(chǎn)品名稱 |
SVG p12 |
商品貨號 |
B165770 |
Organism |
Homo sapiens, human |
Tissue |
brain |
Cell Type |
astroglia; SV40 transformed |
Product Format |
frozen |
Morphology |
fibroblast |
Culture Properties |
adherent |
Biosafety Level |
2 [Cells contain polyomavirus DNA sequences]
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 |
fetus, first trimester |
Applications |
The are susceptible to infection by JC virus, and may be useful in, detecting and cultivating other human neurotropic viruses.
|
Storage Conditions |
liquid nirogen vapor phase |
Disclosure |
This material is cited in a US or other Patent and may not be used to
infringe the claims. Depending on the wishes of the Depositor, ATCC may be
required to inform the Patent Depositor of the party to which the material was
furnished. This material may not have been produced or characterized by ATCC. |
Derivation |
The SVG p12 cell line was established by transfecting cultured human fetal glial cells from brain material dissected from 8 to 12 week old embryos with DNA from an ori - mutant of SV40. |
Genes Expressed |
SV40 T protein; glial fibrillary acidic protein (GFAP) |
Cellular Products |
SV40 T protein; glial fibrillary acidic protein (GFAP) |
Virus Susceptibility |
JC polyomavirus
|
Comments |
The cells express SV40 T antigen.
These cells were recently found to contain infectious BK polyomavirus (BKPyV) of UT strain and a spectrum of defective mutants of this virus.
RefHenriksen, S et al. The human fetal glial cell line SVG p12 contains infectious BK polyomavirus (BKPyV). J. Virol. 2014 Apr 23. [Epub ahead of print] PubMed: 24760884 |
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 |
- 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. Seed new flasks (75 cm2) with 5 X 105 cells.
- Incubate cultures at 37°C.
Medium Renewal: 2 to 3 times per week |
Cryopreservation |
Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO Storage temperature: liquid nirogen vapor phase |
Culture Conditions |
Temperature: 37°C |
STR Profile |
Amelogenin: X,Y
CSF1PO: 10,11,12
D13S217: 8,13,14
D16S5396: 10,11,12
D5S818: 11,12,14
D7S820: 10,12,13
TH01: 6,7,9.3
TPOX: 8,10,11
vWA: 15,16,18,19 |
Name of Depositor |
The United States of America |
U.S. Patent Number |
|
References |
Major EO. Immortal line of human fetal glial cells. US Patent 4,707,448 dated Nov 17 1987
Henriksen, S et al. The human fetal glial cell line SVG p12 contains infectious BK polyomavirus (BKPyV). J. Virol. 2014 Apr 23. [Epub ahead of print] PubMed: 24760884
|