-
平臺編號：bio-68077
-
國際編號：CRL-2050?
-
細胞信息： ZF4
-
規(guī)格：frozen
-
用途：ATCC原裝細胞
-
服務(wù)費用：
加載中…… - 訂購
-
注意事項：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）
ZF4
年限：1 day old embryo
ATCC Number：CRL-2050?
器官來源：胚胎
是否是腫瘤細胞：0
物種來源：斑馬魚
細胞形態(tài)：成纖維樣
數(shù)量：大量
運輸方式：凍存運輸
生長狀態(tài)：貼壁生長
規(guī)格：1mg Designations: ZF4
Depositors: ?W Driever
Biosafety Level:1
Shipped: frozen
Medium & Serum: See Propagation Growth Properties:adherent
Organism: Danio rerio deposited as Brachydanio rerio
Morphology:fibroblast
Source: Organ: embryo
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.
Cytogenetic Analysis:hyperploid; range = 110 to 120
Age: 1 day old embryo
Comments:The ZF4 cell line was established from 1-day-old zebrafish embryos.
The cells are cultivated at 28C, and can be used as a transfection host.
ZF4 cells are killed within 10 days by culturing in medium containing 0.8 to 1.0 mg/ml G418.
Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated DMEM:F12 Medium Catalog No. 30-2006. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Temperature: 28.0°C
Growth Conditions: NOTE: DO NOT USE EDTA TO DISSOCIATE THE CELLS.
Subculturing: Protocol:
Remove and discard culture medium.
Briefly rinse the cell layer with 0.25% (w/v) Trypsin solution to remove all traces of serum that contains trypsin inhibitor.
Add 2.0 to 3.0 ml of Trypsin solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes). .
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 28?C.
Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended
Medium Renewal: 2 to 3 times per week
Preservation: Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
Storage temperature: liquid nitrogen vapor phase
Related Products:Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2006
recommended serum:ATCC 30-2020
References: 24398: Driever W, Rangini Z. Characterization of a cell line derived from zebrafish (Brachydanio rerio) embryos. In Vitro Cell. Dev. Biol. Anim. 29A: 749-754, 1993. PubMed: 8407719
ATCC Number：CRL-2050?
器官來源：胚胎
是否是腫瘤細胞：0
物種來源：斑馬魚
細胞形態(tài)：成纖維樣
數(shù)量：大量
運輸方式：凍存運輸
生長狀態(tài)：貼壁生長
規(guī)格：1mg Designations: ZF4
Depositors: ?W Driever
Biosafety Level:1
Shipped: frozen
Medium & Serum: See Propagation Growth Properties:adherent
Organism: Danio rerio deposited as Brachydanio rerio
Morphology:fibroblast
Source: Organ: embryo
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.
Cytogenetic Analysis:hyperploid; range = 110 to 120
Age: 1 day old embryo
Comments:The ZF4 cell line was established from 1-day-old zebrafish embryos.
The cells are cultivated at 28C, and can be used as a transfection host.
ZF4 cells are killed within 10 days by culturing in medium containing 0.8 to 1.0 mg/ml G418.
Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated DMEM:F12 Medium Catalog No. 30-2006. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Temperature: 28.0°C
Growth Conditions: NOTE: DO NOT USE EDTA TO DISSOCIATE THE CELLS.
Subculturing: Protocol:
Remove and discard culture medium.
Briefly rinse the cell layer with 0.25% (w/v) Trypsin solution to remove all traces of serum that contains trypsin inhibitor.
Add 2.0 to 3.0 ml of Trypsin solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes). .
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 28?C.
Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended
Medium Renewal: 2 to 3 times per week
Preservation: Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
Storage temperature: liquid nitrogen vapor phase
Related Products:Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2006
recommended serum:ATCC 30-2020
References: 24398: Driever W, Rangini Z. Characterization of a cell line derived from zebrafish (Brachydanio rerio) embryos. In Vitro Cell. Dev. Biol. Anim. 29A: 749-754, 1993. PubMed: 8407719
