SU.86.86细胞
年限： 57 years
数量： 大量
运输方式： 冻存运输
ATCC Number： CRL-1837™
器官来源： 胰腺
相关**： 导管癌
生长状态： 贴壁生长
是否是肿瘤细胞： 1
物种来源： 人
细胞形态： 上皮样
Designations: SU.86.86
SU.86.86细胞Depositors: WD Holder
Biosafety Level: 1
Shipped: frozen
Medium & Serum: See Propagation
Growth Properties: adherent
Organism: Homo sapiens
Morphology: epithelial
Source: Organ: pancreas
Disease: ductal carcinoma
Derived from metastatic site: liver
Cellular Products: carcinoembryonic antigen CEA)
Permits/Forms: In addition to the MTA mentioned above, other ATCC and/or regulatory permits may be required for the transfer of this ATCC material. Anyone purchasing ATCC material is ultimately responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.
Tumorigenic: Yes
DNA Profile (STR): SU.86.86细胞Amelogenin: X
CSF1PO: 10,11
D13S317: 11,12
D16S539: 11,13
D5S818: 7,13
D7S820: 8,11
THO1: 9.3
TPOX: 8
vWA: 17
Age: 57 years
Gender: female
Ethnicity: Caucasian
Comments: The cells can be lysed completely in vitro by autologous and allogeneic lymphokine activated killer (LAK) cells in the presence of interleukin 2 (IL-2). They are relatively insensitive to autologous and allogeneic natural killer (NK) cell lysis.
Propagation: SU.86.86细胞ATCC complete growth medium: The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, Catalog No. 30-2001. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
Subculturing: Protocol: Volumes used in this protocol are for 75 cm2 flask; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes. 1. Remove and discard culture medium.2. Briefly rinse the cell layer with 0.25% (w/v) Trypsin-0.53 mM EDTA solution to remove all traces of serum, which contains trypsin inhibitor.3. Add 2.0 to 3.0 ml of Trypsin-EDTA solution to flask and place at 37�C to facilitate dispersal. Observe cells within 5 to 10 minutes under an inverted microscope 4. Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting. 5. To remove trypsin-EDTA solution, transfer cell suspension to a centrifuge tube and spin at approximately 125 xg for 5 to10 minutes.6. Discard supernatant and resuspend cells in fresh growth medium. Add appropriate aliquots of cell suspension to new culture vessels.Recommended seeding densities of 5 X 10(3) to 4 X 10(4) viable cells/cm27. Place culture vessels in incubators at 37�C.Note: subcultures can also be prepared by scraping the cells from the floor of the flask. Add fresh medium, aspirate the scraped cells to disperse them and dispense into new flasks.
Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:3 is recommended by depositor
Medium Renewal: 2 to 3 times per week
Preservation: Freeze medium: Culture medium ,40% ; DMSO,10% ; FBS, 50% FBS..
Storage temperature: liquid nitrogen vapor phase
References: 2159: Drucker BJ, et al. A new human pancreatic carcinoma cell line produced for adoptive immunotherapy studies with lymphokine-activated killer cells in nude mice. SU.86.86细胞In Vitro Cell. Dev. Biol. 24: 1179-1187, 1988. PubMed: 3264833
