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R1

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  • 2025年11月19日
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    • 询价记录
    • 文献和实验
    • 技术资料
    • 运输方式：

      冻存运输

    • 细胞形态：

      球形

    • 库存：

      大量

    • 年限：

      3.5 days embryo, blastocyst

    • 器官来源：

      胚胎

    • 生长状态：

      贴壁生长

    • 组织来源：

      inner cell mass

    • 品系：

      129X1 x 129S1

    • ATCC Number：

      SCRC-1011™

    • 物种来源：

      小鼠

    • 是否是肿瘤细胞：

      0

    • 细胞类型：

      胚胎干细胞

    Designations: R1
    Depositors:  A Nagy
    Biosafety Level: 1
    Shipped: frozen
    Medium & Serum: See Propagation
    Growth Properties: adherent
    Organism: Mus musculus
    Morphology: spherical colony
    Source: Organ: embryo
    Strain: 129X1 x 129S1
    Tissue: inner cell mass
    Cell Type: embryonic stem cell;
    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: Prior to purchase, for-profit commercial institutions must obtain a license agreement. For instructions on how to proceed, please contact ATCC 's Office of Licensing and Business Development at licensing@ATCC .org or 703 365 2773.
    Isolation: Isolation date: August, 1991
    Applications: However, about 20% of subclones derived from passage #14 had the original developmental potential of R1 when tested by tetraploid aggregates [PubMed: 8378314]].
    No live offspring were produced from cells older than passage #14.* .
    Pluripotency of R1 was initially tested by tetraploid embryo <-> ES aggregates for completely ES derived development [PubMed: 8378314].
    The R1 cell line was established in August 1991, from a 3.5 day blastocyst produced by crossing two 129 substrains (129S1/SvImJ and 129X1/SvJ).
    The segregation could result in several coat types, from albino, through light brown, to black, depending on the genetic background of the partner of the germline chimaera.
    Age: 3.5 days embryo, blastocyst
    Gender: male
    Comments: The R1 cell line was established in August 1991, from a 3.5 day blastocyst produced by crossing two 129 substrains (129S1/SvImJ and 129X1/SvJ). The cells are heterozygous for the c locus (+/c (ch)) and for the pink eye locus (+/p). In the F1 generation the coat color is uniform agouti, while in the F2 these two coat color genes segregate. The segregation could result in several coat types, from albino, through light brown, to black, depending on the genetic background of the partner of the germline chimaera.
    Pluripotency of R1 was initially tested by tetraploid embryo <-> ES aggregates for completely ES derived development [PubMed: 8378314]. They were also tested by diploid embryo <-> ES aggregates and blastocyst injection for germline transmission in chimeras [PubMed: 8361547]. At early passages (up to passage #14), one third of the completely R1-derived newborns generated by tetraploid embryo <-> R1 aggregates survived. No live offspring were produced from cells older than passage #14.* .
    However, about 20% of subclones derived from passage #14 had the original developmental potential of R1 when tested by tetraploid aggregates [PubMed: 8378314]]. R1-derived animals reached adulthood and were fertile. The genetically altered lines derived from R1 gave high efficiency of germline transmission either by injecting them into C57 blastocyst or aggregating them with CD-1 or ICR outbred 8-cell stage embryos. More than 90% of the individual K.O. clones went to germline (n>60) by aggregation chimeras.
    *Current ATCC stocks of R1 cells are beyond passage 14. Current stocks of alternative subclone of R1 cells, designated R1/E (ATCC SCRC-1036 ), are below passage 14 and have been shown to be germline competent.
    Propagation: ATCC complete growth medium: Mouse ES Cell Basal Medium
    Atmosphere: air, 95%; carbon dioxide (CO2), 5%
    Temperature: 37.0°C
    Subculturing: Protocol: Establishing and maintaining your culture: To insure the highest level of viability, be sure to warm media to 37�C before using it on the cells.
    1. Plate mitotically arrested MEF (CF-1) (ATCC SCRC-1040 ) as a feeder layer at approximately 1.5 to 2.0 X 106 cells/T25 at least one day before plating R1 cells (see product sheet for mitotically arrested MEF for protocol). One hour before thawing the vial of R1 ES cells, perform a 100% medium change using 10 ml of complete growth medium for ES cells.
    2. Thaw the vial by gentle agitation in a 37°C water bath. To reduce the possibility of contamination, keep the O-ring and cap out of the water. Thawing should be rapid (approximately 90 seconds).
    3. Remove the vial from the water bath as soon as the contents are thawed, and decontaminate by dipping in or spraying with 70% ethanol. All of the operations from this point on should be carried out under strict aseptic conditions.
    4. Transfer the vial s contents plus 5 ml of complete growth medium for ES cells to a 15 ml centrifuge tube. Use an additional 1 ml of media to rinse the vial and transfer the liquid to the 15 ml tube. Add 4 ml of complete growth medium for ES cells to bring the total volume to 10 ml.
    5. Spin the cells at 270 xg for 5 min. Aspirate the supernatant and resuspend the pellet in 5 ml of complete growth medium for ES cells.
    6. Add the 5 ml of cell suspension to the T75 flask containing feeder cells and 10 ml complete growth medium for ES cells.
    7. Incubate the culture at 37°C in a humidified 5% CO2 /95% air incubator. Perform a 100% medium change every day, passage cells every 1 to 2 days.
    Subculturing Procedure: To insure the highest level of viability, be sure to warm media and Trypsin/EDTA to 37°C before using it on the cells. Volumes used in this protocol are for T75 flasks. Proportionally adjust the volumes for culture vessels of other sizes. A split ratio of 1:4 to 1:7 every 1 to 2 days is recommended. Plating densities should range from 3 to 4 X 106 cells/ T75. Note: If the colonies are close to or touching each other the culture is overgrown . Overgrowth will result in differentiation.
    1. Prepare enough flasks with MEFs as stated above in step #1.
    2. Aspirate the medium from the flask(s) with R1 ES cells.
    3. Wash with PBS (Ca+2/Mg+2-free, ATCC cat# SCRR-2201).
    4. Add 3.0 ml of 0.25% (w/v) Trypsin / 0.53 mM EDTA solution (ATCC cat # 30-2101) and place in incubator. After about one minute the ES colonies will dissociate and all cells will detach from the flask.
    5. Dislodge the cells by gently tapping the side of the flask then wash the cells off with 7-10 ml of fresh culture medium. Triturate cells several times with a 10 ml pipette in order to dissociate the cells into a single-cell suspension.
    6. Spin the cells at 270 xg for 5 min. Aspirate the supernatant.
    7. Resuspend in 30 to 50 ml of fresh culture medium, depending on the split ratio.
    8. Aspirate the medium from 4 to 7 feeder layer flasks and replace it with 15 ml/flask of R1 cell suspension.
    9. Incubate the culture at 37°C in a humidified 5% CO2 /95% air incubator. Perform a 100% medium change every day, passage cells every 1 to 2 days.

    Interval: Every one to two days
    Subcultivation Ratio: A subcultivation ratio of 1:4 to 1:7 is recommended
    Medium Renewal: Every day
    Preservation: Freeze medium: Complete growth medium supplemented with an additional 10% FBS and 10% DMSO.
    Storage temperature: liquid nitrogen vapor phase
    Related Products: Derivative: ATCC SCRC-1036
    References: 57459: Matise M, et alProduction of targeted embryonic stem cell clonesIn: Matise M, et alGene Targeting: A Practical ApproachOxfordOxford University Press101-132, 1999
    71506: Nagy A, et al. Derivation of completely cell culture-derived mice from early-passage embryonic stem cells. Proc. Natl. Acad. Sci. USA : 8424-8428, 1993. PubMed: 8378314
    71870: Wood SA, et al. Non-injection methods for the production of embryonic stem cell-embryo chimaeras. Nature 365: 87-89, 1993. PubMed: 8361547
    71871: Nagy A, Rossant JProduction and analysis of ES-cell aggregation chimerasIn: Nagy A, Rossant JGene Targeting: A Practical ApproachOxfordOxford University Press177-206, 1999

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