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TeloHAEC cells细胞株 BioVector NTCC质粒载体菌种细胞基因保藏中心

  • 价  格:¥49865
  • 货  号:TeloHAEC cells细胞株
  • 产  地:北京
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TeloHAEC cells细胞株

TeloHAEC cell line
Cat No.: NTCC-CRL4052

Organism Homo sapiens, human
Tissue aorta
Cell Type endothelial
Product Format frozen
Morphology endothelial
Culture Properties adherent
Biosafety Level 2  [Cells containing SV40 viral DNA sequences]
Disease normal
Age 34 years old
Gender female
Applications TeloHAEC (NTCC CRL-4052) cells retain important endothelial cell characteristics such as  CD31/PECAM-1 marker expression and LDL functional uptake; the cells also show effective inflammatory response upon TNFα treatment and increase proliferation upon VEGF stimulation.  When co-cultured with fibroblasts, TeloHAEC cells can also form neoangiogenic tubular networks in vitro, which are responsive to VEGF stimulation and suramin inhibition.
Karyotype This is a diploid cell line of female origin with a consistent normal kayrotype at low and high passages
Images

Derivation TeloHAEC is a clonal cell line immortalized by stably expressing human telomerase catalytic subunit hTERT
Clinical Data female 
34
Antigen Expression Positive for CD31/PECAM-1 expression  and capable of uptaking Low Density Lipoprotein (LDL).

Complete Growth Medium The base medium for this cell line is Vascular Cell Basal Medium (NTCC PCS-100-030), supplemented with Vascular Endothelial Cell Growth Kit-VEGF (NTCC PCS-100-041).   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 cm2 flasks; 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 Dulbecco's Phosphate Buffered Saline (DPBS, NTCC 30-2200) and discard rinse solution.
3.Add 2.0 to 3.0 mL room temperature Trypsin-EDTA for Primary Cells (NTCC 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 103 to 8.0 x 103 viable cells/cm2 to new culture vessels.
Medium Renewal: Every 2-3 days.
Cryopreservation 90% FBS, 10% DMSO
Culture Conditions Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Temperature: 37°C

STR Profile
D5S818:  12        
D13S317: 9, 12
D7S820: 10, 11        
D16S539: 12, 13
vWA: 15, 16             
Amelogenin:  X
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.

Supplier来源:BioVector NTCC Inc.
TEL电话:+86-010-53513060
Website网址: http://www.biovector.net

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