CL-0109
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Product Introduction
| Cell Name | HK-2 |
| Synonyms | Hk-2;HK2;Human Kidney-2 |
| Cellosaurus Accession | CVCL_0302 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Epithelial-like |
| Tissue | Kidney; cortex; proximal tubule |
| Age | Adult |
| Sex | Male |
| 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. |
| Complete Medium | MEM, with NEAA [PM150410]+10% Nutrient+1% Supplement |
| Incubation Atmosphere | Air, 95%; CO₂, 5% |
| Temperature | 37℃ |
| Subcultivation Ratio | 1:2-1:4 |
| Medium Renewal | 2 to 3 times per week |
| Dissociation Duration | 2-3 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 | General Freezing Medium [PB180436] |
| 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. |
| Background | HK-2 cells are derived from normal human renal proximal tubule cells immortalized by transduction with the HPV‑16 E6/E7 genes. The recombinant retroviral vector pLXSN 16 E6/E7 was transfected into the ecotropic packaging cell line Psi‑2; virus produced by Psi‑2 cells was then used to infect the amphotropic packaging cell line PA317. Finally, viral particles generated by PA317 cells were used to transduce normal renal cortical proximal tubule cells. Although pLXSN 16 E6/E7 contains a neomycin resistance gene, G418 selection was not used to isolate transduced clones. Southern blot and FISH analyses demonstrated that HK-2 cells are derived from a single clone, and PCR analysis confirmed the presence of the E6/E7 genes in the HK-2 genome. |
| Receptor Expression | epidermal growth factor (EGF), expressed |
| Gene Expression | alkaline phosphatase; gamma glutamyltranspeptidase; leucine aminopeptidase; acid phosphatase; cytokeratin; alpha 3, beta 1 integrin; fibronectin |
| Biosafety Level | BSL-2 |
Documents
Publications
Journal: CELL BIOLOGY INTERNATIONAL (2024) IF: 3.3
DOI: 10.1002/cbin.12258
Product Cited: MEM, with NEAA Medium, HK-2 Cells Line
Journal: Frontiers in Bioscience-Landmark (2024) IF: 3.3
Product Cited: HK-2 Cells Line, RPMI-1640 Medium, Caki-1 Cells Line, Penicillin-Streptomycin Solution, 100 ×, 786-O [786-0] Cells Line, MEM, with NEAA Medium, McCoy's 5A Medium, A-498 Cells Line, Fetal Bovine Serum
Journal: TOXICOLOGY AND APPLIED PHARMACOLOGY (2024) IF: 3.3
DOI: 10.1016/j.taap.2024.117181
Product Cited: 769-P Cells Line, HK-2 Cells Line, Caki-2 Cells Line, 786-O [786-0] Cells Line, Caki-1 Cells Line
Journal: EXPERIMENTAL CELL RESEARCH (2024) IF: 3.3
DOI: 10.1016/j.yexcr.2024.114341
Product Cited: MEM Medium, MEM (Glucose free) Medium, HK-2 Cells Line
Journal: FREE RADICAL RESEARCH (2024) IF: 3.3
DOI: 10.1080/10715762.2024.2330413
Product Cited: HK-2 Cells Line
