產品名稱 |
MIA PaCa-2 |
商品貨號 |
B165157 |
Organism |
Homo sapiens, human |
Tissue |
pancreas |
Cell Type |
epithelial cell |
Product Format |
frozen |
Morphology |
attached epithelial with floating rounded cells |
Culture Properties |
adherent, single cells and loosely attached clusters |
Biosafety Level |
1
Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country. |
Disease |
carcinoma |
Age |
65 years |
Gender |
male |
Ethnicity |
Caucasian |
Storage Conditions |
liquid nitrogen vapor phase |
Karyotype |
This is a hypotriploid human cell line. The modal chromosome number is 61. Sixteen to 20 marker chromosomes are commonly found in a cell. A few normal chromosomes are absent. |
Images |
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Derivation |
The MIA PaCa-2 cell line was established by A. Yunis, et al. in 1975 from tumor tissue of the pancreas obtained from a 65-year-old Caucasian male.
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Clinical Data |
65 years
Caucasian
male
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Genes Expressed |
human colony stimulating factor, subclass I (CSF-I); plasminogen activator |
Cellular Products |
human colony stimulating factor, subclass I (CSF-I); plasminogen activator |
Comments |
The established cell line reportedly has a doubling time of about 40 hours and a colony-forming efficiency in soft agar of approximately 19%.
Hybridomas have been made against the CSF-I produced by this line ATCC HB-8207 (F1A3-23) and ATCC HB-8208 (F18 AF1).
The line is sensitive to asparaginase. |
Complete Growth Medium |
The base medium for this cell line is ATCC-formulated Dulbecco's Modified Eagle's Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%; horse serum to a final concentration of 2.5%.
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Subculturing |
Remove medium, and rinse with 0.25% trypsin, 0.53 mM EDTA solution. Remove the solution and add an additional 1 to 2 mL of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37°C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Corning® T-75 flasks (catalog #430641) are recommended for subculturing this product.
Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:8 is recommended
Medium Renewal: 2 to 3 times per week |
Cryopreservation |
Freeze medium: Complete growth medium 95%; DMSO, 5% Storage temperature: liquid nitrogen vapor phase |
Culture Conditions |
Temperature: 37°C |
STR Profile |
D5S818: 12,13
D13S317: 12,13
D7S820: 12,13
D16S539: 10,13
vWA: 15
THO1: 9,10
Amelogenin: X
TPOX: 9
CSF1PO: 10 |
Isoenzymes |
G6PD, B |
Name of Depositor |
A Yunis |
Deposited As |
Homo sapiens |
Year of Origin |
1975 |
References |
Wu M, et al. Purification and characterization of a plasminogen activator secreted by cultured human pancreatic carcinoma cells. Biochemistry 16: 1908-1913, 1977. PubMed: 15590
Fountzilas G, et al. Comparative effects of selected drug combinations on the growth of a human pancreatic carcinoma cell line (MIA PaCa-2). J. Natl. Cancer Inst. 76: 37-43, 1986. PubMed: 3455740
Robertson JF, et al. Effect of gastrointestinal hormones and synthetic analogues on the growth of pancreatic cancer. Int. J. Cancer 63: 69-75, 1995. PubMed: 7558455
Yunis AA, et al. Human pancreatic carcinoma (MIA PaCa-2) in continuous culture: sensitivity to asparaginase. Int. J. Cancer 19: 128-135, 1977. PubMed: 832918
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Cross References |
Nucleotide (GenBank) :
M64592
Human macrophage colony stimulating factor (M-CSF-1) mRNA, complete cds.
Nucleotide (GenBank) :
M76744
Homo sapiens alternatively spliced biliary glycoprotein (BGP) mRNA, 3' end of cds.
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