宁波泰斯拓生物

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SVEC4-10EE2

货号 TS210851
中文名称 null
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产品名称: SVEC4-10EE2
商品货号: TS210851
Organism: Mus musculus, mouse
Tissue: axillary lymph node; vascular epithelium
Cell Type: endothelial, SV40 transformed
Product Format: frozen
Morphology: cobblestone
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: adult
Gender: male
Strain: C3H/HeJ
Applications:
SVEC4-10EE2 is an endothelial cell line derived from the same solid tumor as SVEC4-10EHR1 (see CRL-2161) in a nude mouse injected with SVEC4-10 (see ATCC CRL-2181).
The cells were cloned in 1989 by limiting dilution, and are distinguished by their inability to differentiate on a synthetic basement-like membrane.
The cells exhibit a stable cobblestone morphology in contrast to its sibling from the same tumor (SVEC4-10EHR1).
Storage Conditions: liquid nitrogen vapor phase
Derivation:
SVEC4-10EE2 is an endothelial cell line derived from the same solid tumor as SVEC4-10EHR1 (see CRL-2161) in a nude mouse injected with SVEC4-10 (see ATCC CRL-2181).
Clinical Data:
male
Antigen Expression:
H-2 K; Factor VIII related antigen; VCAM
Receptor Expression:
high affinity receptors for low density lipoprotein (LDL)
Genes Expressed:
H-2 K; Factor VIII related antigen; VCAM
Tumorigenic: Yes
Effects:
Yes, the cells induce spindle tumors with some of the histopathologic characteristics of human Kaposi Sarcoma after a latency period of approximately 14 weeks
Comments:
SVEC4-10EE2 is an endothelial cell line derived from the same solid tumor as SVEC4-10EHR1 (see CRL-2161) in a nude mouse injected with SVEC4-10 (see ATCC CRL-2181).
The cells were cloned in 1989 by limiting dilution, and are distinguished by their inability to differentiate on a synthetic basement-like membrane.
They form tube-like structures in the presence of suramin, a drug which blocks growth factor receptors.
The cells exhibit a stable cobblestone morphology in contrast to its sibling from the same tumor (SVEC4-10EHR1).
The cells express the cell surface major histocompatibility complex class I antigen, H-2 k of the parental cell line, and express Factor VIII related antigen, high affinity receptors for low density lipoprotein and vascular cell adhesion molecule (VCAM).
The cells stain positively for SV40 T antigen.
Complete Growth Medium: Dulbeccos modified Eagles medium with 4 mM L-glutamine adjusted to contain 1.5 g/L sodium bicarbonate and 4.5 g/L glucose, 90%; heat-inactivated horse serum, 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.
  1. Remove and discard culture medium.
  2. Briefly rinse the cell layer with 0.25% (w/v) Trypsin-0.53mM EDTA solution to remove all traces of serum which 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.
  6. Incubate cultures at 37°C.

Subcultivation Ratio: 1:4 to 1:6
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:

Complete growth medium described above supplemented with 5% (v/v) DMSO.xa0 Cell culture tested DMSO is available as ATCC Catalog No. 4-X.

Culture Conditions:
Temperature: 37°C
Atmosphere: Air, 95%; Carbon dioxide (CO2), 5%
Name of Depositor: KA OConnell
Year of Origin: 1989
References:

OConnell KA, Edidin M. A mouse lymphoid endothelial cell line immortalized by simian virus 40 binds lymphocytes and retains functional characteristics of normal endothelial cells. J. Immunol. 144: 521-525, 1990. PubMed: 2153170

OConnell KA, Rudmann AA. Cloned spindle and epithelioid cells from murine Kaposis sarcoma-like tumors are of endothelial origin. J. Invest. Dermatol. 100: 742-745, 1993. PubMed: 8496612

OConnell K, et al. Endothelial cells transformed by SV40 T antigen cause Kaposis sarcomalike tumors in nude mice. Am. J. Pathol. 139: 743-749, 1991. PubMed: 1928299

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.

Biosafety in Microbiological and Biomedical Laboratories, 5th ed. HHS. U.S. Department of Health and Human Services, Centers for Disease Control and Prevention. Washington DC: U.S. Government Printing Office; 2007. The entire text is available online.