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平臺(tái)編號(hào)：bio-68686
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國(guó)際編號(hào)：CRL-1861?
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細(xì)胞信息： EM9
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規(guī)格：frozen
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用途：ATCC原裝細(xì)胞
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服務(wù)費(fèi)用：
加載中…… - 訂購(gòu)
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注意事項(xiàng)：僅用于科學(xué)研究或者工業(yè)應(yīng)用等非醫(yī)療目的不可用于人類或動(dòng)物的臨床診斷或治療，非藥用，非食用（產(chǎn)品信息以出庫為準(zhǔn)）
EM9 (DNA repair mutant of CHO)
生長(zhǎng)狀態(tài)：混合型生長(zhǎng)
是否是腫瘤細(xì)胞：0
物種來源：倉(cāng)鼠
運(yùn)輸方式：凍存運(yùn)輸
器官來源：卵巢
細(xì)胞形態(tài)：上皮樣
ATCC Number：CRL-1861?
數(shù)量：大量
規(guī)格：0.5ml Designations: EM9 (DNA repair mutant of CHO)
Depositors: ?LH Thompson
Biosafety Level:1
Shipped: frozen
Medium & Serum: See Propagation Growth Properties:mixed, adherent 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 ).
EM9 is a repair deficient mutant derived from AA8 (see ATCC CRL-1859 ).
The line was selected for enhanced sensitivity to ethylmethanesulfonate (EMS).
The line is defective in single strand break repair, has a 10 fold higher baseline frequency of sister chromatid exchange relative to AA8 and a 2 fold greater sensitivity to killing by X-rays.
This defect is corrected by the human XRCC1 gene.
Propagation: ATCC complete growth medium: Alpha minimum essential medium without ribonucleosides and deoxyribonucleosides, 90%; fetal bovine serum, 10%
Temperature: 37.0°C
Subculturing: Protocol:
Subcultivation Ratio: A subcultivation ratio of 1:4 to 1:12 is recommended
Medium Renewal: 2 to 3 times per week
Preservation: Freeze medium: Complete growth medium 95%; DMSO, 5%
Storage temperature: liquid nitrogen vapor phase
Related Products:recommended serum:ATCC 30-2020
References: 1771: Thompson LH, et al. A CHO-cell strain having hypersensitivity to mutagens, a defect in DNA strand-break repair, and an extraordinary baseline frequency of sister-chromatid exchange. Mutat. Res. 95: 427-440, 1982. PubMed: 6889677
58396: Thompson LH, et al. A screening method for isolating DNA repair-deficient mutants of CHO cells. Somatic Cell Genet. 6: 391-405, 1980. PubMed: 7404270
是否是腫瘤細(xì)胞：0
物種來源：倉(cāng)鼠
運(yùn)輸方式：凍存運(yùn)輸
器官來源：卵巢
細(xì)胞形態(tài)：上皮樣
ATCC Number：CRL-1861?
數(shù)量：大量
規(guī)格：0.5ml Designations: EM9 (DNA repair mutant of CHO)
Depositors: ?LH Thompson
Biosafety Level:1
Shipped: frozen
Medium & Serum: See Propagation Growth Properties:mixed, adherent 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 ).
EM9 is a repair deficient mutant derived from AA8 (see ATCC CRL-1859 ).
The line was selected for enhanced sensitivity to ethylmethanesulfonate (EMS).
The line is defective in single strand break repair, has a 10 fold higher baseline frequency of sister chromatid exchange relative to AA8 and a 2 fold greater sensitivity to killing by X-rays.
This defect is corrected by the human XRCC1 gene.
Propagation: ATCC complete growth medium: Alpha minimum essential medium without ribonucleosides and deoxyribonucleosides, 90%; fetal bovine serum, 10%
Temperature: 37.0°C
Subculturing: Protocol:
- To subculture attaced cells, remove culture medium.
- The suspended cells are viable and can be used to start new cultures.
- Briefly rinse the cell layer with 0.25% (w/v) Trypsin- 0.53 mM EDTA solution to remove all traces of serum that contains trypsin inhibitor.
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Add 2.0 to 3.0 ml of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).
Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37?C to facilitate dispersal. - Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting.
- Add appropriate aliquots of the cell suspension to new culture vessels.
- Incubate cultures at 37?C.
Subcultivation Ratio: A subcultivation ratio of 1:4 to 1:12 is recommended
Medium Renewal: 2 to 3 times per week
Preservation: Freeze medium: Complete growth medium 95%; DMSO, 5%
Storage temperature: liquid nitrogen vapor phase
Related Products:recommended serum:ATCC 30-2020
References: 1771: Thompson LH, et al. A CHO-cell strain having hypersensitivity to mutagens, a defect in DNA strand-break repair, and an extraordinary baseline frequency of sister-chromatid exchange. Mutat. Res. 95: 427-440, 1982. PubMed: 6889677
58396: Thompson LH, et al. A screening method for isolating DNA repair-deficient mutants of CHO cells. Somatic Cell Genet. 6: 391-405, 1980. PubMed: 7404270
