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平臺編號：bio-69051
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國際編號：ATCC ACS-1011
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細胞信息： ATCC DYR0100
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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（產品信息以出庫為準）
ATCC DYR0100
年限：Newborn
運輸方式：凍存運輸
ATCC Number：ACS-1011?
相關疾?。浩渌膊?br /> 數量：大量
細胞類型：其他細胞類型
是否是腫瘤細胞：0
物種來源：人
規(guī)格：0.5mg Designations: ATCC -DYR0100 Human Induced Pluripotent Stem Cells
Depositors: ?ATCC
Biosafety Level:2 [ATCC highly recommends that protective gloves and clothing always be used and a full face mask always be worn when handling frozen vials.It is important to note that some vials leak when submersed in liquid nitrogen and will slowly fill with liquid nitrogen. Upon thawing, the conversion of the liquid nitrogen back to its gas phase may result in the vessel exploding or blowing off its cap with dangerous force creating flying debris. ]
Shipped: frozen
Medium & Serum: See Propagation Organism: Homo sapiens
Morphology:
Source: Cell Type: Human iPSC
Disease: Normal
Reprogramming Method: Retroviral expression of OCT4, SOX2, KLF4, and MYC genes
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.
Restrictions:This product may be used by investigator for internal research purposes and only in recipient's investigator's laboratory subject to the iPS MTA, the Addendum to the iPS MTA, and any additional third party terms. This product is subject to claims under U.S. Patent Nos. 8,058,065 and 8,048,999, pending patent applications, and foreign counterparts thereof. For information on obtaining additional rights, please contact licensing@ATCC .org .The iPS MTA and Addendum to the iPS MTA are also available at: www.atcc.org .
Age: Newborn
Gender: Male
Ethnicity: Unknown
Propagation: ATCC complete growth medium: CellMatrix? Basement Membrane Gel
CellMatrix? Basement Membrane Gel
Pluripotent Stem Cell SFM XF/FF
Pluripotent Stem Cell SFM XF/FF
Subculturing: This protocol is designed to passage stem cell colonies cultured in a 6 cm dish, using Stem Cell Dissociation Reagent (ATCC ACS-3010 ) to detach the cell colonies. Stem Cell Dissociation Reagent is stored as a 0.5 U/mL working solution at -20°C. The cells should be split at a ratio of 1:4.
Volumes should be adjusted according to the size and number of the tissue culture vessels to be processed.
1. Warm an aliquot of Stem Cell Dissociation Reagent working solution to room temperature.
2. Aspirate and discard the stem cell culture medium.
3. Rinse the cells twice with 4 mL of D-PBS (ATCC 30-2200 ).
4. Add 2 mL of Stem Cell Dissociation Reagent working solution to the dish.
5. Incubate at 37°C for 10 to 15 minutes or until the edges of the individual colonies begin to loosen and fold back. View the dish under the microscope starting at 5 minutes as incubation time will vary depending on the cell line and colony size.
6. Aspirate the Stem Cell Dissociation Reagent and gently rinse the colonies with 4 mL of DMEM: F-12 Medium (ATCC 30-2006 ), taking care not to dislodge the cells during manipulation.
7. Add 2 mL of Pluripotent Stem Cell SFM XF/FF to the dish, and detach the cells by pipetting up and down several times with a 1 mL tip. Take care not to over-pipette the culture into a single-cell suspension as single cells will not establish colonies after seeding.
8. Transfer the cell aggregates to a 15 mL conical tube.
9. Add an additional 3 mL of Pluripotent Stem Cell SFM XF/FF to the dish to collect any remaining cells. Transfer this rinse to the 15 mL conical tube containing the cell aggregates.
10. Centrifuge the cell aggregates at 200 x g for 5 minutes.
11. Aspirate the supernatant and discard.
12. Gently resuspend the pellet by pipetting up and down 5 to 6 times with a 1 mL tip, maintaining the small cell aggregates.
13. Plate the cells as desired on feeder or feeder-free cultures in the presence of 10 ?M ROCK Inhibitor Y27632* (ATCC ACS-3030 ) to the cell culture medium is recommended.
*ROCK Inhibitor Y27632 has been shown to reduce dissociation-induced apoptosis.
14. Incubate the culture at 37°C in a humidified 5% CO2 /95% air incubator. Perform a 100% medium change every day. Passage the cells every 4 to 5 days (80% confluent).
Preservation: For optimal results, cryopreserve stem cell colonies when the cell cultures are 80% confluent. This protocol is designed to cryopreserve stem cell colonies cultured in a 6 cm dish.
1. Detach stem cell colonies from the dish as described in the recommended subculturing protocol (steps 1-11). Gently tap the bottom of the tube to loosen the cell pellet.
2. Take the Stem Cell Freezing Medium (ATCC ACS-3020 ) from storage and swirl to mix. Keep cold. Decontaminate by dipping in or spraying with 70% alcohol.
3. Add 2 mL of cold Stem Cell Freezing Medium to the tube. Gently resuspend the pellet by pipetting up and down 5-6 times with a 1 mL tip, maintaining the cell aggregates.
4. Immediately transfer 1 mL each of the cell suspension into two labeled cryovials.
5. Freeze the cells gradually at a rate of -1°C/min until the temperature reaches -70°C to -80°C. An isopropanol freezing container also may be used.
6. The cells should not be left at -80°C for more than 24 to 48 hours. Once at -80°C, frozen cryovials should be transferred to the vapor phase of liquid nitrogen for long-term storage.
Related Products:Stem Cell Dissociation Reagent (ATCC ACS-3010)
D-PBS (ATCC 30-2200)
ROCK Inhibitor Y27632 (ATCC ACS-3030)
DMEM: F12 (ATCC 30-2006)
Stem Cell Freezing Media (ATCC ACS-3020)
運輸方式：凍存運輸
ATCC Number：ACS-1011?
相關疾?。浩渌膊?br /> 數量：大量
細胞類型：其他細胞類型
是否是腫瘤細胞：0
物種來源：人
規(guī)格：0.5mg Designations: ATCC -DYR0100 Human Induced Pluripotent Stem Cells
Depositors: ?ATCC
Biosafety Level:2 [ATCC highly recommends that protective gloves and clothing always be used and a full face mask always be worn when handling frozen vials.It is important to note that some vials leak when submersed in liquid nitrogen and will slowly fill with liquid nitrogen. Upon thawing, the conversion of the liquid nitrogen back to its gas phase may result in the vessel exploding or blowing off its cap with dangerous force creating flying debris. ]
Shipped: frozen
Medium & Serum: See Propagation Organism: Homo sapiens
Morphology:
Source: Cell Type: Human iPSC
Disease: Normal
Reprogramming Method: Retroviral expression of OCT4, SOX2, KLF4, and MYC genes
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.
Restrictions:This product may be used by investigator for internal research purposes and only in recipient's investigator's laboratory subject to the iPS MTA, the Addendum to the iPS MTA, and any additional third party terms. This product is subject to claims under U.S. Patent Nos. 8,058,065 and 8,048,999, pending patent applications, and foreign counterparts thereof. For information on obtaining additional rights, please contact licensing@ATCC .org .The iPS MTA and Addendum to the iPS MTA are also available at: www.atcc.org .
Age: Newborn
Gender: Male
Ethnicity: Unknown
Propagation: ATCC complete growth medium: CellMatrix? Basement Membrane Gel
CellMatrix? Basement Membrane Gel
Pluripotent Stem Cell SFM XF/FF
Pluripotent Stem Cell SFM XF/FF
Subculturing: This protocol is designed to passage stem cell colonies cultured in a 6 cm dish, using Stem Cell Dissociation Reagent (ATCC ACS-3010 ) to detach the cell colonies. Stem Cell Dissociation Reagent is stored as a 0.5 U/mL working solution at -20°C. The cells should be split at a ratio of 1:4.
Volumes should be adjusted according to the size and number of the tissue culture vessels to be processed.
1. Warm an aliquot of Stem Cell Dissociation Reagent working solution to room temperature.
2. Aspirate and discard the stem cell culture medium.
3. Rinse the cells twice with 4 mL of D-PBS (ATCC 30-2200 ).
4. Add 2 mL of Stem Cell Dissociation Reagent working solution to the dish.
5. Incubate at 37°C for 10 to 15 minutes or until the edges of the individual colonies begin to loosen and fold back. View the dish under the microscope starting at 5 minutes as incubation time will vary depending on the cell line and colony size.
6. Aspirate the Stem Cell Dissociation Reagent and gently rinse the colonies with 4 mL of DMEM: F-12 Medium (ATCC 30-2006 ), taking care not to dislodge the cells during manipulation.
7. Add 2 mL of Pluripotent Stem Cell SFM XF/FF to the dish, and detach the cells by pipetting up and down several times with a 1 mL tip. Take care not to over-pipette the culture into a single-cell suspension as single cells will not establish colonies after seeding.
8. Transfer the cell aggregates to a 15 mL conical tube.
9. Add an additional 3 mL of Pluripotent Stem Cell SFM XF/FF to the dish to collect any remaining cells. Transfer this rinse to the 15 mL conical tube containing the cell aggregates.
10. Centrifuge the cell aggregates at 200 x g for 5 minutes.
11. Aspirate the supernatant and discard.
12. Gently resuspend the pellet by pipetting up and down 5 to 6 times with a 1 mL tip, maintaining the small cell aggregates.
13. Plate the cells as desired on feeder or feeder-free cultures in the presence of 10 ?M ROCK Inhibitor Y27632* (ATCC ACS-3030 ) to the cell culture medium is recommended.
*ROCK Inhibitor Y27632 has been shown to reduce dissociation-induced apoptosis.
14. Incubate the culture at 37°C in a humidified 5% CO2 /95% air incubator. Perform a 100% medium change every day. Passage the cells every 4 to 5 days (80% confluent).
Preservation: For optimal results, cryopreserve stem cell colonies when the cell cultures are 80% confluent. This protocol is designed to cryopreserve stem cell colonies cultured in a 6 cm dish.
1. Detach stem cell colonies from the dish as described in the recommended subculturing protocol (steps 1-11). Gently tap the bottom of the tube to loosen the cell pellet.
2. Take the Stem Cell Freezing Medium (ATCC ACS-3020 ) from storage and swirl to mix. Keep cold. Decontaminate by dipping in or spraying with 70% alcohol.
3. Add 2 mL of cold Stem Cell Freezing Medium to the tube. Gently resuspend the pellet by pipetting up and down 5-6 times with a 1 mL tip, maintaining the cell aggregates.
4. Immediately transfer 1 mL each of the cell suspension into two labeled cryovials.
5. Freeze the cells gradually at a rate of -1°C/min until the temperature reaches -70°C to -80°C. An isopropanol freezing container also may be used.
6. The cells should not be left at -80°C for more than 24 to 48 hours. Once at -80°C, frozen cryovials should be transferred to the vapor phase of liquid nitrogen for long-term storage.
Related Products:Stem Cell Dissociation Reagent (ATCC ACS-3010)
D-PBS (ATCC 30-2200)
ROCK Inhibitor Y27632 (ATCC ACS-3030)
DMEM: F12 (ATCC 30-2006)
Stem Cell Freezing Media (ATCC ACS-3020)
