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產(chǎn)品資料

SU.86.86細(xì)胞

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產(chǎn)品名稱: SU.86.86細(xì)胞
產(chǎn)品型號(hào): SU.86.86
產(chǎn)品展商: HZbscience
產(chǎn)品文檔: 無相關(guān)文檔

簡(jiǎn)單介紹

SU.86.86細(xì)胞應(yīng)如何避免細(xì)胞污染,細(xì)胞污染的種類可分成**、酵母菌、霉菌、病毒和霉?jié){菌。主要的污染原因?yàn)闊o菌操作技術(shù)不當(dāng)、操作室環(huán)境不佳、污染之血清和污染之細(xì)胞等。嚴(yán)格之無菌操作技術(shù)、清潔的環(huán)境、與品質(zhì)良好之細(xì)胞來源和培養(yǎng)基配制是減低污染之*好方法。SU.86.86細(xì)胞何時(shí)須更換培養(yǎng)基?視細(xì)胞生長(zhǎng)密度而定,或遵照細(xì)胞株基本數(shù)據(jù)上之更換時(shí)間,按時(shí)更換培養(yǎng)基即可。


SU.86.86細(xì)胞  的詳細(xì)介紹

SU.86.86細(xì)胞

年限: 57 years

數(shù)量: 大量

運(yùn)輸方式: 凍存運(yùn)輸

ATCC Number: CRL-1837?

器官來源: 胰腺

相關(guān)**: 導(dǎo)管癌

生長(zhǎng)狀態(tài): 貼壁生長(zhǎng)

是否是腫瘤細(xì)胞: 1

物種來源: 人

細(xì)胞形態(tài): 上皮樣

Designations: SU.86.86

SU.86.86細(xì)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細(xì)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細(xì)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細(xì)胞In Vitro Cell. Dev. Biol. 24: 1179-1187, 1988. PubMed: 3264833

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