宁波泰斯拓生物

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TeloHAEC

货号 TS165714
中文名称 null
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产品简介
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产品名称: TeloHAEC
商品货号: TS165714
Organism: Homo sapiens, human
Tissue: aorta
Cell Type: endothelial
Product Format: frozen
Morphology: endothelial
Culture Properties: adherent
Biosafety Level: 2 xa0Cells containing SV40 viral 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.

Disease: normal
Age: 34 years old
Gender: female
Applications: TeloHAEC (TS165714) cells retain important endothelial cell characteristics such as xa0CD31/PECAM-1 marker expression and LDL functional uptake; the cells also show effective inflammatory response upon TNFα treatment and increase proliferation upon VEGF stimulation. xa0When co-cultured with fibroblasts, TeloHAEC cells can also form neoangiogenic tubular networks in vitro, which are responsive to VEGF stimulation and suramin inhibition.
Storage Conditions: liquid nitrogen vapor phase
Karyotype: This is a diploid cell line of female origin with a consistent normal kayrotype at low and high passages
Images: CRL-4052 Cell Micrograph TS165714 CD31 Expression Angiogensis Co-Culture with BJ
Derivation: TeloHAEC is a clonal cell line immortalized by stably expressing human telomerase catalytic subunit hTERT
Clinical Data: femalexa0

34

Antigen Expression: Positive for CD31/PECAM-1 expression xa0and capable of uptaking Low Density Lipoprotein (LDL).
Complete Growth Medium: The base medium for this cell line is Vascular Cell Basal Medium (ATCC PCS-100-030), supplemented with Vascular Endothelial Cell Growth Kit-VEGF (ATCC PCS-100-041). xa0 Optional: Add 0.3ug/mL Puromycin(Santa Cruz Biotech: sc-108071A). Note: Do not filter complete medium.
Subculturing: Volumes used in this protocol are for 75 cm2xa0flasks; proportionally reduce or increase amount of dissociation solutions for culture vessels of other sizes.

Subculture when the culture is about 90% confluent.
  1. Remove and discard spent medium.
  2. Briefly rinse the cells with Dulbeccos Phosphate Buffered Saline (DPBS, ATCC 30-2200) and discard rinse solution.
  3. Add 2.0 to 3.0 mL room temperature Trypsin-EDTA for Primary Cells (ATCC PCS-999-003) to the flask. Incubate at 37°C for 5 min (until cells have detached).
  4. Neutralize trypsin by adding an equal volume of room temperature 2% FBS in DPBS.
  5. Centrifuge cells at 250 x g for 5 min at room temperature.
  6. Remove supernatant. Resuspend pellet in 6.0 to 8.0 mL Complete Growth Medium.
  7. Count cells, and seed 5.0 x 103xa0to 8.0 x 103xa0viable cells/cm2xa0to new culture vessels.
Medium Renewal:xa0Every 2-3 days.
Cryopreservation: 90% FBS, 10% DMSO
Culture Conditions: Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Temperature: 37°C
STR Profile:

D5S818: xa012 xa0 xa0 xa0 xa0
D13S317: 9, 12
D7S820: 10, 11 xa0 xa0 xa0 xa0
D16S539: 12, 13
vWA: 15, 16 xa0 xa0 xa0 xa0 xa0 xa0xa0
Amelogenin: xa0X
TPOX: 8
CSF1PO: 11, 12
TH01: 6, 8
Population Doubling Level (PDL): As part of our quality control, we have tested this cell line for its ability to grow for a minimum of 15 population doublings after recovery from cryopreservation. We have also compared its karyotype, telomerase expression level, growth rate, morphology and tissue-specific markers when first recovered from cryopreservation with that of cells at 10+ population doublings to ensure that there is no change in these parameters and that the cells are capable of extended proliferation.
Name of Depositor: ATCC