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產(chǎn)品資料

UV135細(xì)胞

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產(chǎn)品名稱: UV135細(xì)胞
產(chǎn)品型號: UV135
產(chǎn)品展商: HZbscience
產(chǎn)品文檔: 無相關(guān)文檔

簡單介紹

UV135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。主要的污染原因為無菌操作技術(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。UV135細(xì)胞何時須更換培養(yǎng)基?視細(xì)胞生長密度而定,或遵照細(xì)胞株基本數(shù)據(jù)上之更換時間,按時更換培養(yǎng)基即可。


UV135細(xì)胞  的詳細(xì)介紹

UV135細(xì)胞

是否是腫瘤細(xì)胞: 0

物種來源: 倉鼠

器官來源: 卵巢

運(yùn)輸方式: 凍存運(yùn)輸

ATCC Number: CRL-1867?

細(xì)胞形態(tài): 上皮樣

生長狀態(tài): 單層、懸浮

數(shù)量: 大量

Designations: UV135 (UV sensitive mutant of CHO)

Depositors: LH Thompson

Biosafety Level: 1

UV135細(xì)胞Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: monolayer and suspension

Organism: Cricetulus griseus

Morphology: epithelial-like


Source: Organ: ovary

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.

Gender: female

Comments: This line is a derivative of the CHO-K1 cell line (see ATCC CCL-61).

UV135 is a UV sensitive line derived from AA8 (see ATCC CRL-1859).

The line is defective in nucleotide excision repair, is sensitive to bulky adduct mutagens and belongs to excision repair complementation group 5.

Propagation: UV135細(xì)胞ATCC complete growth medium: Alpha minimum essential medium without ribonucleosides and deoxyribonucleosides, 90%; fetal bovine serum, 10%

Subculturing: Subcultivation Ratio: A subcultivation ratio of 1:4 to 1:12 is recommended

Medium Renewal: 2 to 3 times per week

To subculture attached cells, remove the medium and rinse the cells with fresh 0.25% trypsin, 0.03% EDTA.

Let the culture sit at 37C until the cells detach (about 5 minutes).

Add fresh medium, aspirate and transfer to new flasks.

The suspended cells are viable and can be used to start new cultures.

Doubling Time: 13 hrs

References: 1767: Thompson LH, et al. Repair of DNA adducts in asynchronous CHO cells and the role of repair in cell killing and mutation induction in synchronous cells treated with 7-bromomethylbenz[a]anthracene. Somatic Cell Mol. Genet. 10: 183-194, 1984. PubMed: 6584989

1768: Thompson LH, et al. Genetic diversity of UV-sensitive DNA repair mutants of Chinese hamster ovary cells. Proc. Natl. Acad. Sci. USA 78: 3734-3737, 1981. PubMed: 6943579

1769: Hoy CA, et al. Defective DNA cross-link removal in Chinese hamster cell mutants hypersensitive to bifunctional alkylating agents. Cancer Res. 45: 1737-1743, 1985. PubMed: 3919945

1770: Busch D, et al.UV135細(xì)胞 Summary of complementation groups of UV-sensitive CHO cell mutants isolated by large-scale screening. Mutagenesis 4: 349-354, 1989. PubMed: 2687628

21855: . Cellular responses to DNA damage. New York: Liss; 1983.

32479: Bessho T, et al. Initiation of DNA interstrand cross-link repair in humans: the nucleotide excision repair system makes dual incisions 5" to the cross-linked base and removes a 22- to 28-nucleotide-long damage-free strand. Mol. Cell. Biol. 17: 6822-6830, 1997. PubMed: 9372913

32924: Reardon JT, et al. Isolation and characterization of two human transcription factor IIH (TFIIH)-related complexes: ERCC2/CAKand TFIIH. Proc. Natl. Acad. Sci. USA 93: 6482-6487, 1996. PubMed: 8692841

58395: Thompson LH, et al. UV135細(xì)胞Hypersensitivity to mutation and sister-chromatid-exchange induction in CHO cell mutants defective in incising DNA containing UV lesions. Somatic Cell Genet. 8: 759-773, 1982. PubMed: 7163954

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