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        產(chǎn)品詳情
        • 產(chǎn)品名稱:Psi2 DAP 小鼠胚胎成纖維細(xì)胞

        • 產(chǎn)品型號:CRL-1949
        • 產(chǎn)品廠商:美國標(biāo)準(zhǔn)生物品收藏中心(ATCC)
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        CRL-1949 Psi2 DAP 小鼠胚胎成纖維細(xì)胞,原代細(xì)胞|細(xì)胞系|細(xì)胞株|菌種;細(xì)胞庫管理規(guī)范,提供的細(xì)胞株背景清楚,提供參考文獻(xiàn)和培養(yǎng)條件!
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        CRL-1949 Psi2 DAP 小鼠胚胎成纖維細(xì)胞
        ATCC® Number:  CRL-1949?       
        Designations:  Psi2 DAP 
        Depositors:   CL Cepko 
        Biosafety Level: 1 
        Shipped:  frozen 
        Medium & Serum:  See Propagation 
        Growth Properties: adherent
        Organism: Mus musculus (mouse) 
        Morphology: fibroblast

         
        Source: Strain: NIH/Swiss
        Organ: embryo
        Disease: normal
        Cellular Products: a human placental alkaline phosphatase transducing vector 
        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. 
         
        Reverse Transcript: positive 
        Age:  embryo 
        Comments: This line produces a vector that can infect mouse cells.
        Psi2 DAP cells produce a vector that encodes the human placental alkaline phosphatase gene and the neomycin resistance gene.
        The line was derived from Psi2 cells by insertion of a recombinant retrovirus genome (DAP).
        Cells infected with the vector produced by Psi2 DAP cells express histochemically detectable alkaline phosphatase which can be used as a marker to follow their fate in vivo.
        The cells may produce helper virus.
        To assay for helper virus, and for other retrovirus techniques, see Cepko, C.L.
        Lineage analysis and immortalization of neural cells via retrovirus vectors in Neuromethods, Molecular Neurobiological Techniques 16:117-219, Boulton, A.A., Baker, G.B. and Campagnoni, A.T., Eds., Humana Press, Clifton, NJ, 1989.
        Propagation:  ATCC complete growth medium: Dulbecco's modified Eagle's medium with 4.5 g/L glucose, 90%; bovine calf serum, 10%
         
        Subculturing:  Subcultivation Ratio: A subcultivation ratio of 1:10 to 1:50 is recommended
        Medium Renewal: Every 2 to 3 days
        Remove medium, add fresh 0.25% trypsin, 0.02% EDTA and allow the flask to sit at room temperature (or 37C) until the cells detach (2 to 3 minutes). Add fresh medium, aspirate and dispense into new flasks.
        References: 22598: Fields-Berry SC, et al. A recombinant retrovirus encoding alkaline phosphatase confirms clonal boundary assignment in lineage analysis of murine retina. Proc. Natl. Acad. Sci. USA 89: 693-697, 1992. PubMed: 1731342 
         
         

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