JCRB0177.0 KP-1N
Cell information
Important Notice(s)JCRB0177.0 KP-1N, JCRB0177.1 KP-1NL細胞の由来の問題について
Problem of identity in JCRB0177.0 KP-1N and JCRB0177.1 KP-1NL.
Cell type:general cells (View Pricing Information)
| JCRB No. | JCRB0177.0 | Cell Name | KP-1N |
|---|---|---|---|
| Profile | Stop providing for the issue of quality control. (Please contact us for more information) Human pancreatic cancer cell line established in nude mice. | Other Name | |
| Animal | human | Strain | |
| Genus | Homo | Species | sapiens |
| Sex | M | Age | 69 |
| Identity | available | Tissue for Primary Cancer | pancreas |
| Case history | Pancreatic tumor | Metastasis | Yes |
| Tissue Metastasized | liver metastasis | Genetics | |
| Life Span | infinite | Crisis PDL | |
| Morphology | epithelial-like | Character | Human pancreatic cancer cell line established in nude mice. |
| Classify | tumor | Established by | Kono,A. et. al. |
| Registered by | Iguchi,H. | Regulation for Distribution | |
| Comment | The STR-PCR pattern was identical with the KP-1NL(JCRB0177.0). | Year | 2001 |
| Medium | RPMI1640 medium with 10% fetal bovine serum | Methods for Passages | Cells are harvested after treatment with 0.02% EDTA and 0.1% trypsin. Subculture when cells reached to subconfluent. |
| Cell Number on Passage | 1-2 x 10^5 cells/T25 frask | Race | Japanese |
| CO2 Conc. | Tissue Sampling | pancreatic tumor | |
| Tissue Type |
| Detection of virus genome fragment by Real-time PCR | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Detected DNA Virus | tested | Detected RNA Virus | not tested | ||||||
| CMV | - | parvoB19 | - |
-/negative. +/positive. nt/not tested. (positive (+) does not immediately mean the production of infectious viral particles.) |
|||||
| EBV | - | HBV | - | ||||||
| HHV6 | - | HTLV-1 | - | ||||||
| HHV7 | - | HTLV-2 | - | ||||||
| BKV | - | HIV-1 | - | ||||||
| JCV | - | HIV-2 | - | ||||||
| ADV | - | HPV18 | - | ||||||
| Notes | |||||||||
| Reference | |
|---|---|
| Pubmed id:9735394 | Alteration of the CDKN2A gene in pancreatic cancers: Is it a late event in the progression of pancreatic cancer? Sugimoto Y,Morita R,Hikiji K,Imura G,Ogata Y,Yasuda D,Kono A,Iguchi H Int J Oncol. 1998 Oct;13(4):669-76 |
| Pubmed id:21607521 | Alterations of the p53 tumor-suppressor gene and ki-ras oncogene in human pancreatic cancer-derived cell-lines with different metastatic potential. Iguchi H,Morita R,Yasuda D,Takayanagi R,Ikeda Y,Takada Y,Shimazoe T,Nawata H,Kono A Oncol Rep. 1994 Nov;1(6):1223-7 |
| Pubmed id:2172194 | Establishment and characterization of human pancreatic cancer cell lines in tissue culture and in nude mice. Ikeda Y,Ezaki M,Hayashi I,Yasuda D,Nakayama K,Kono A Jpn J Cancer Res. 1990 Oct;81(10):987-93 |
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LOT Information
Viability/Growth rate/Cell number are represented as actual values measured at lot presentation in JCRB, but are not guaranteed values. Additionally, the doubling time is a rough value measured during passages.| Cell No. | JCRB0177.0 | Cell Name | |
|---|---|---|---|
| LOT No. | 05222006 | Lot Specification | distribution |
| Medium | RPMI1640 medium with 10% fetal bovine serum (FBS lot; GIBCO 4218333S) | Temperature | 37 C |
| Cell Density at Seeding | 4 - 7 x 10^4 cells/ml | Methods for Passages | 0.1% trypsin and 0.02% EDTA in Ca, Mg-free PBS |
| Doubling Time | approx. 1 day | Cell Number in Vial (cells/1ml) | 2.4 x 10^6 |
| Viability at cell freezing (%) | 98.7 | Antibiotics Used | free |
| Passage Number | Unknown (18 at bank) | PDL | |
| Sterility: MYCOPLASMA | - | Sterility: BACTERIA | - |
| Sterility: FUNGI | - | Isozyme Analysis | Confirmed as human by NP, G6PD (type B), AST, MD. |
| Chromosome Mode | Chromosome Information | ||
| Surface Antigen | DNA Profile (STR) | ||
| Adhesion | Yes | Exoteric Gene | |
| Medium for Freezing | 10% DMSO, 20% FBS - RPMI1640 | CO2 Conc. | 5% |
| Viability immediately after thawing (%) | Additional information |
| Cell No. | JCRB0177.0 | Cell Name | KP-1N |
|---|---|---|---|
| LOT No. | 08122002 | Lot Specification | distribution |
| Medium | RPMI1640 medium with 10% fetal calf serum (Mitsubishi PVF001). | Temperature | 37 C |
| Cell Density at Seeding | 2.1 x 10^4 cells/sq.cm. | Methods for Passages | Cells are harvested after treatment with 0.1% trypsin. Medium change twice a week. Subculture once a week. |
| Doubling Time | NT | Cell Number in Vial (cells/1ml) | 1.4 x 10^6 |
| Viability at cell freezing (%) | 98.2 | Antibiotics Used | free |
| Passage Number | P16* | PDL | NT |
| Sterility: MYCOPLASMA | - | Sterility: BACTERIA | - |
| Sterility: FUNGI | - | Isozyme Analysis | G6PD(type B), NP and LDH examined. Human,not HeLa. |
| Chromosome Mode | NT | Chromosome Information | NT |
| Surface Antigen | NT | DNA Profile (STR) | D5S818:11,13 D13S317:11 D7S820:8,10 D16S539:11 VWA:15 TH01:7,8 AM:X TPOX:8,11 CSF1PO:10,12 |
| Adhesion | Yes | Exoteric Gene | NT |
| Medium for Freezing | Culture medium containing 5% DMSO. | CO2 Conc. | 5 % |
| Viability immediately after thawing (%) | Additional information |
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| Cell No. | JCRB0177.0 | Cell Name | KP-1N |
|---|---|---|---|
| LOT No. | 08242001 | Lot Specification | distribution |
| Medium | RPMI1640 medium with 10 % fetal calf serum(Intergen RB52405) and 5ug/ml MC210. | Temperature | 37 C |
| Cell Density at Seeding | 2.0 x 10^4 cells/sq.cm. | Methods for Passages | Cells harvested after treatment with 0.1% trypsin. Subculture once or twice a week and medium change in between. |
| Doubling Time | NT | Cell Number in Vial (cells/1ml) | 1.3 x 10^6 |
| Viability at cell freezing (%) | 99.3 | Antibiotics Used | MC210 (5 ug/ml). Only for this cell culture. |
| Passage Number | P8* | PDL | NT |
| Sterility: MYCOPLASMA | + | Sterility: BACTERIA | - |
| Sterility: FUNGI | - | Isozyme Analysis | G6PD(typeB), NP, LDH examined. Human, not HeLa. |
| Chromosome Mode | NT | Chromosome Information | NT |
| Surface Antigen | NT | DNA Profile (STR) | |
| Adhesion | Yes | Exoteric Gene | NT |
| Medium for Freezing | Culture medium with 5% DMSO, but no MC210 included. | CO2 Conc. | 5 % |
| Viability immediately after thawing (%) | Additional information |
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