CL-0118
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Product Introduction
| Cell Name | HT-29 |
| Synonyms | HT 29;HT29 |
| Cellosaurus Accession | CVCL_0320 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Epithelial-like |
| Disease | colorectal cancer cells |
| Tissue | Colon |
| Age | 44Y |
| Sex | Female |
| 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 | McCoy's 5A [PM150710]+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 | 3-5 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 | HT-29 cells were established in 1964 by J. Fogh from a primary tumor via explant culture in F12 medium supplemented with 15% fetal bovine serum (FBS). The cell line is currently maintained in McCoy's 5A medium with the same serum concentration. HT-29 cells are tumorigenic in both nude mice and steroid-treated hamsters, and synthesize IgA, CEA, TGF-β-binding proteins, and mucins. |
| Tumorigenic | Yes, in nude mice; forms well differentiated adenocarcinoma consistent with colonic primary (grade I); tumors also form in steroid treated hamsters. |
| Receptor Expression | human adrenergic alpha2A, urokinase receptor (u-PAR), vitamin D (moderate expression), urokinase receptor (u-PAR); vitamin D (moderate expression), human adrenergic alpha2A |
| Gene Expression | secretory component of IgA; carcinoembryonic antigen (CEA); transforming growth factor beta binding protein; mucin, myc+; ras+; myb+; fos+; sis+; p53+; abl -; ros -; src -, Blood Type A; Rh+; HLA A1, A3, B12, B17, Cw5, HT-29 cells are negative for CD4, but there is cell surface expression of galactose ceramide (a possible alternative receptor for HIV). |
| Biosafety Level | BSL-1 |
Documents
Publications
Journal: Cytometry Part A (2021) IF: 3.7
DOI: 10.1002/cyto.a.24475
Product Cited: HT-29 Cells Line
Journal: Journal Of Physiology And Biochemistry (2021) IF: 3.4
DOI: 10.1007/s13105-021-00796-y
Product Cited: HT-29 Cells Line
Journal: Oncology Letters (2021) IF: 2.9
Product Cited: HCT 116 Cells Line, HT-29 Cells Line, MET-5A Cells Complete Medium
Journal: Oncology Letters (2021) IF: 2.9
Product Cited: HT-29 Cells Line
Journal: Pathology Research And Practice (2021) IF: 2.8
DOI: 10.1016/j.prp.2021.153520
Product Cited: LoVo Cells Line, SW48 Cells Line, HT-29 Cells Line, DLD-1 Cells Line
