![Lec2 [originally named Pro-5WgaRII6A]](http://family998.com/static/images/cells-no_picture.jpg)
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平臺編號：bio-69076
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國際編號：CRL-1736?
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細胞信息： Lec2
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規(guī)格：frozen
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用途：ATCC原裝細胞
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服務(wù)費用：
加載中…… - 訂購
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注意事項：僅用于科學研究或者工業(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）
Lec2 [originally named Pro-5WgaRII6A]
細胞形態(tài)：上皮樣
運輸方式：凍存運輸
ATCC Number：CRL-1736?
是否是腫瘤細胞：0
物種來源：倉鼠
數(shù)量：大量
器官來源：卵巢
生長狀態(tài)：單層（少量懸浮）
規(guī)格：0.5mg Designations: Lec2 [originally named Pro-5WgaRII6A]
Depositors: ?P Stanley
Biosafety Level:1
Shipped: frozen
Medium & Serum: See Propagation Growth Properties:monolayer or suspension
Organism: Cricetulus griseus
Morphology:epithelial
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 mutant clone derived from the parental CHO clone Pro-5 (a proline auxotroph, see ATCC CRL-1781 ) by selection for resistance to wheat germ agglutinin.
The cells exhibit a drastic reduction in the transport of CMP-sialic acid into the Golgi compartment, and may be useful for studying the role of sialic acid in the function and compartmentalization of glycosylated macromolecules.
The cells are proline auxotrophs and must be grown in a medium that contains proline (40 mg/L).
The population contains Pro+ revertants at high frequency (approximately 1 in 25 cells), and should be cloned if it is desired to use the Pro- marker in complementation studies.
Propagation: ATCC complete growth medium: Alpha minimum essential medium, 90%; fetal bovine serum, 10%
Subculturing: Protocol: Remove medium, add fresh 0.25% trypsin, let sit for 2 to 3 minutes, remove trypsin and let the culture sit at room temperature for 5 to 10 minutes or until the cells detach. Add fresh medium, aspirate and dispense into new flasks.
Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended
Medium Renewal: 2 to 3 times per week
References: 22626: Deutscher SL, et al. Translocation across Golgi vesicle membranes: a CHO glycosylation mutant deficient in CMP-sialic acid transport. Cell 39: 295-299, 1984. PubMed: 6498937
58070: Stanley P, Siminovitch L. Complementation between mutants of CHO cells resistant to a variety of plant lectins. Somatic Cell Genet. 3: 391-405, 1977. PubMed: 601679
運輸方式：凍存運輸
ATCC Number：CRL-1736?
是否是腫瘤細胞：0
物種來源：倉鼠
數(shù)量：大量
器官來源：卵巢
生長狀態(tài)：單層（少量懸浮）
規(guī)格：0.5mg Designations: Lec2 [originally named Pro-5WgaRII6A]
Depositors: ?P Stanley
Biosafety Level:1
Shipped: frozen
Medium & Serum: See Propagation Growth Properties:monolayer or suspension
Organism: Cricetulus griseus
Morphology:epithelial
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 mutant clone derived from the parental CHO clone Pro-5 (a proline auxotroph, see ATCC CRL-1781 ) by selection for resistance to wheat germ agglutinin.
The cells exhibit a drastic reduction in the transport of CMP-sialic acid into the Golgi compartment, and may be useful for studying the role of sialic acid in the function and compartmentalization of glycosylated macromolecules.
The cells are proline auxotrophs and must be grown in a medium that contains proline (40 mg/L).
The population contains Pro+ revertants at high frequency (approximately 1 in 25 cells), and should be cloned if it is desired to use the Pro- marker in complementation studies.
Propagation: ATCC complete growth medium: Alpha minimum essential medium, 90%; fetal bovine serum, 10%
Subculturing: Protocol: Remove medium, add fresh 0.25% trypsin, let sit for 2 to 3 minutes, remove trypsin and let the culture sit at room temperature for 5 to 10 minutes or until the cells detach. Add fresh medium, aspirate and dispense into new flasks.
Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended
Medium Renewal: 2 to 3 times per week
References: 22626: Deutscher SL, et al. Translocation across Golgi vesicle membranes: a CHO glycosylation mutant deficient in CMP-sialic acid transport. Cell 39: 295-299, 1984. PubMed: 6498937
58070: Stanley P, Siminovitch L. Complementation between mutants of CHO cells resistant to a variety of plant lectins. Somatic Cell Genet. 3: 391-405, 1977. PubMed: 601679
