NCI-H1395 Cells
Product number:
305118
General information
Description | This cell line was established in 1986 from a 55-year-old female smoker (15 pack years) with non-small cell lung carcinoma. Another cell line, NCI-BL1395 (BL1395), is a lymphoblastoid line from the same patient. |
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Organism | Human |
Tissue | Lung |
Disease | Lung adenocarcinoma |
Synonyms | NCI-H1395, H-1395, NCIH1395 |
Characteristics
Age | 55 years |
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Gender | Female |
Ethnicity | European |
Morphology | Lymphoblast |
Growth properties | Adherent |
Identifiers / Biosafety / Citation
Citation | NCI-H1395 (Cytion catalog number 305118) |
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Biosafety level | 1 |
Expression / Mutation
Handling
Culture Medium | RPMI 1640, w: 2.1 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a) |
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Medium supplements | Supplement the medium with 10% FBS |
Passaging solution | Accutase |
Subculturing | Remove the old medium from the adherent cells and wash them with PBS that lacks calcium and magnesium. For T25 flasks, use 3-5 ml of PBS, and for T75 flasks, use 5-10 ml. Then, cover the cells completely with Accutase, using 1-2 ml for T25 flasks and 2.5 ml for T75 flasks. Let the cells incubate at room temperature for 8-10 minutes to detach them. After incubation, gently mix the cells with 10 ml of medium to resuspend them, then centrifuge at 300xg for 3 minutes. Discard the supernatant, resuspend the cells in fresh medium, and transfer them into new flasks that already contain fresh medium. |
Split ratio | 1: 3 to 1: 4 |
Fluid renewal | 2 to 3 times per week |
Freeze medium | CM-1 (Cytion catalog number 800100) or CM-ACF (Cytion catalog number 806100) |
Handling of cryopreserved cultures | NCI-H1395 cells are shipped in a deep-frozen state on dry ice. Upon receipt, confirm that the vial remains frozen. For storage, place the cryovial immediately at temperatures below -150 degrees. If you plan to culture the cells immediately, swiftly thaw the vial by shaking it in a 37 degrees water bath with clean water and an antimicrobial agent for 40-60 seconds. Remove the vial once a small ice clump persists, ensuring it remains cold. Proceed with all subsequent steps under aseptic conditions. In a sterile flow hood, disinfect the cryovial with 70% ethanol. Then, gently open the vial and transfer the cell suspension into a 15 ml centrifuge tube pre-filled with 8 ml of room temperature culture medium. Gently mix the cells. For cell separation, centrifuge at 300 x g for 3 minutes and dispose of the supernatant. Skipping centrifugation is optional, although any residual freezing medium should be removed after 24 hours. Resuspend the pellet gently in 10 ml of fresh culture medium and divide between two T25 culture flasks. Follow the subculture protocol for subsequent steps. |
Quality control / Genetic profile / HLA
Sterility | Mycoplasma contamination is rigorously excluded using both PCR-based assays and luminescence-based mycoplasma detection methods. To ensure there is no bacterial, fungal, or yeast contamination, cell cultures are subjected to daily visual inspections. |
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STR profile |
Amelogenin: x,x
CSF1PO: 12
D13S317: 10,14
D16S539: 11,13
D5S818: 12
D7S820: 8
TH01: 6,9.3
TPOX: 8
vWA: 14,17
D3S1358: 15
D21S11: 29
D18S51: 12,14
Penta E: 7
Penta D: 12
D8S1179: 12,14
FGA: 18,23
D6S1043: 18,19
D2S1338: 17,24
D12S391: 20,22
D19S433: 13,16
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