CL-0675
$ 600.00
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1×10^6Cells/Vial×2Vials
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Product Introduction
General information
| Cell Name | PUMC-HUVEC-T1 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Endothelial-like |
| Tissue | Umbilical vein |
Handling information
| Instructions | 1. Check all containers for leakage or breakage. 2. Remove the frozen cells from the dry ice packaging and immediately transfer them to liquid nitrogen (liquid or vapor phase) for long-term cryopreservation. 3. This cell line has a finite lifespan; please control passage numbers carefully. 4. This cell line is relatively challenging to culture; dedicated culture medium is recommended. 5. During cell culture, a small number of floating cells and dark granules will be present. Dark granules will gradually increase with culture time; normal culture can be continued after medium exchange or subculture. |
| Complete Medium | Complete culture medium for PUMC-HUVEC-T1 |
| Incubation Atmosphere | Air, 95%; CO₂, 5% |
| Temperature | 37℃ |
| Subcultivation Ratio | 1:2-1:3 |
| Medium Renewal | 2 to 3 times per week |
| Dissociation Duration | 1-2 min |
| Subculturing Procedure | 1. Remove the culture medium from the T25 cell culture flask. 2. Add approximately 2 mL of PBS. Gently tilt the flask side to side until the PBS covers the entire bottom, then aspirate and discard the PBS. 3. Add 1 mL of 0.25% trypsin solution (containing EDTA). Gently tilt the flask side to side until the trypsin solution covers the entire bottom of the flask. 4. Incubate the cells at 37°C. Observe the cells under an inverted microscope and terminate digestion once the cells round up and detach. To avoid clumping, do not agitate the cells by tapping or shaking the flask during detachment. 5. Add 3 mL of complete culture medium to terminate digestion and disperse into a single cell suspension. 6. Collect the cell suspension and centrifuge at 1200 rpm (approximately 250 ×g) for 3 minutes. Carefully aspirate and discard the supernatant. 7. Add fresh complete culture medium, pipette gently several times to resuspend the cells, and seed them at the appropriate ratio into a new culture flask. Loosen the cap or use a vented cap for incubation. |
| Freeze Medium | 90% FBS+10% DMSO |
| Storage Conditions | For long-term cryopreservation, cryovials should be stored in liquid nitrogen at −150°C to −196°C. Storage at −80°C is restricted to short-term interim use only. |
Documents
Publications
Suppression of angiogenesis and tumor growth by recombinant T4 phages displaying extracellular domain of vascular endothelial growth factor receptor 2
Journal: Archives of Virology (2018) IF: 2.7
DOI: 10.1007/s00705-018-4026-0
Product Cited: MS1 Cells Line, PUMC-HUVEC-T1 Cells Line
Hollow Au–Cu Nanocomposite for Real-Time Tracing Photothermal/Antiangiogenic Therapy
Journal: Advanced Healthcare Materials (2017) IF: 10
Product Cited: 4T1 Cells Line, PUMC-HUVEC-T1 Cells Line
Weighted Gene Co-expression Network Analysis Identifies FKBP11 as a Key Regulator in Acute Aortic Dissection through a NF-kB Dependent Pathway
Journal: Frontiers in Physiology (2017) IF: 4
Product Cited: PUMC-HUVEC-T1 Cells Line
Rapamycin/DiR loaded lipid-polyaniline nanoparticles for dual-modal imaging guided enhanced photothermal and antiangiogenic combination therapy
Journal: Journal Of Controlled Release (2016) IF: 10.8
DOI: 10.1016/j.jconrel.2016.07.005
Product Cited: PUMC-HUVEC-T1 Cells Line
