宁波泰斯拓生物

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SVG p12

货号 TS210838
中文名称 null
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产品简介
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产品名称: SVG p12
商品货号: TS210838
Organism: Homo sapiens, human
Tissue: brain
Cell Type: astroglia; SV40 transformed
Product Format: frozen
Morphology: fibroblast
Culture Properties: adherent
Biosafety Level: 2 xa0Cells 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.xa0

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 Eagles 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:
  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 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. Seed new flasks (75 cm2) with 5 X 105 cells.
  6. 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