AsPC-1

Zellname

Beschreibung

Bestell-Nr.

Einheit

Preis, Euro

AsPC-1

Humane Pankreas Adenokarzinom Zell-Linie

300158

cryovial

265,00

AsPC-1

Humane Pankreas Adenokarzinom Zell-Linie

330158

vital

335,00



Designation:AsPC-1
Depositor:Tan
Organism:Homo sapiens (human)
Ethnicity:Caucasian
Age/Stage:62 years of age
Gender:female
Tissue:Pancreas (ascites)
Celltype:adenocarcinoma
Growth Properties:monolayer
Description:The line was derived from nude mouse xenografts initiated with cells from the ascites of a patient with cancer of the pancreas.
Culture Medium:RPMI 1640 medium supplemented with L-glutamine, 1 mM sodium pyruvate and 10% fetal bovine serum.
Subculturing:Remove medium and rinse with fresh 0.02% EDTA (versene) solution. Add 0.025% trypsin/0.02% versene solution and let the culture sit at 37°C until the cells detach (control under the microscope). Add fresh, FBS containing medium, resuspend in fresh medium and dispense into new flasks.
Split Ratio:A ratio of 1:3 to 1:6 is recommended
Fluid Renewal:2 to 3 times weekly
Freeze Medium:CM-1 (CLS ∙ Cell Lines Service)
Sterility:Tests for mycoplasma, bacteria and fungi were negative
Biosafety Level:1
Products:carcinoembryonic antigen (CEA); human pancreas associated antigen; human pancreas specific antigen; mucin


References:

Tan MH et al. Differential localization of human pancreas cancer-associated antigen and carcinoembryonic antigen in homologous pancreatic tumoral xenograft. J Natl Cancer Inst 67: 563-9, 1981.
Chen WH et al. Human pancreatic adenocarcinoma: in vitro and in vivo morphology of a new tumor line established from ascites. In Vitro 18: 24-34, 1982.
Loor R et al. Use of pancreas-specific antigen in immunodiagnosis of pancreatic cancer. Clin Lab Med 2: 567-78, 1982.
Tan MH and Chu TM. Charcterization of the tumorigenic and metastatic properties of a human pancreatic tumor cell line (AsPC-1) implanted orthotopically into nude mice. Tumour Biol 6: 89-98, 1985.
Lan MS et al. Polypeptide core of a human pancreatic tumor mucin antigen. Cancer Res 50: 2997-3001, 1990.
Nuevemann D et al. Stable expression of temperature-sensitive p53 : a suitable model to study wild-type p53 function in pancreatic carcinoma cells. Oncol Rep 16: 575-9, 2006.
El-Rayes BF et al. Potentation of the effect of erlotinib by genistein in pancreatic cancer: the role of Akt and nuclear factor-kappaB. Cancer Res 66: 10553-9, 2006.

 

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