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MDCK (NBL-2)

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    • 详细信息
    • 询价记录
    • 文献和实验
    • 技术资料
    • 物种来源

    • 是否是肿瘤细胞

      0

    • 库存

      大量

    • 细胞形态

      上皮样

    • 生长状态

      贴壁生长

    • 年限

      adult

    • 相关疾病

      正常

    • ATCC Number

      CCL-34™

    • 器官来源

      肾脏

    • 运输方式

      冻存运输

    Designations: MDCK (NBL-2)
    Depositors:  S Madin, NB Darby
    Biosafety Level: 1
    Shipped: frozen
    Medium & Serum: See Propagation
    Growth Properties: adherent
    Organism: Canis familiaris
    Morphology: epithelial

    Source: Organ: kidney
    Disease: normal
    Cellular Products: keratin
    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.
    Isolation: Isolation date: September, 1958
    Applications: transfection host
    Virus Susceptibility: Human Coxsackievirus B 5
    Reovirus type 2
    Adeno-associated virus 4
    Vaccinia virus
    Vesicular stomatitis virus
    Adeno-associated virus 5
    Human Coxsackievirus B 3
    Human Coxsackievirus B 4
    Human poliovirus 2
    Cytogenetic Analysis: Polyploidy 0.2%. Two large submetacentric chromosomes noted, presumably X chromosomes, and one or two additional chromosomes with median or submedian centromeres.
    Age: adult
    Gender: female
    Comments: The MDCK cell line was derived from a kidney of an apparently normal adult female cocker spaniel, September, 1958, by S.H. Madin and N.B. Darby. The cells are positive for keratin by immunoperoxidase staining. MDCK cells have been used to study processing of beta amyloid precursor protein and sorting of its proteolytic products.
    Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Eagle's Minimum Essential Medium, Catalog No. 30-2003. 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: 37.0°C
    Subculturing: Protocol:
    1. Remove and discard culture medium.
    2. Rinse the cell layer twice with 0.25% (w/v) Trypsin - 0.53 mM EDTA solution to remove all traces of serum that contains trypsin inhibitor.
    3. Add 2.0 to 3.0 ml of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).
      Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37�C to facilitate dispersal.
    4. Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting.
    5. Add appropriate aliquots of the cell suspension to new culture vessels.
    6. Incubate cultures at 37�C.

    Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:6 is recommended
    Medium Renewal: Every 2 to 3 days
    Preservation: Freeze medium: Complete growth medium 95%; DMSO, 5%
    Storage temperature: liquid nitrogen vapor phase
    Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2003
    recommended serum:ATCC 30-2020
    0.25% (w/v) Trypsin - 0.53 mM EDTA in Hank' BSS (w/o Ca++, Mg++):ATCC 30-2101
    Cell culture tested DMSO:ATCC 4-X
    References: 18385: Didier ES, et al. Characterization of Encephalitozoon (Septata) intestinailis isolates cultured from nasal mucosa and bronchoalveolar lavage fluids of two AIDS patients. J. Eukaryot. Microbiol. 43: 34-43, 1996. PubMed: 8563708
    22808: Haass C, et al. Polarized sorting of beta-amyloid precursor protein and its proteolytic products in MDCK cells is regulated by two independent signals. J. Cell Biol. 128: 537-547, 1995. PubMed: 7860629
    25972: Gaush CR, et al. Characterization of an established line of canine kidney cells (MDCK). Proc. Soc. Exp. Biol. Med. 122: 931-935, 1966. PubMed: 5918973
    28301: Loffler S, et al. CD9, a tetraspan transmembrane protein, renders cells susceptible to canine distemper virus. J. Virol. 71: 42-49, 1997. PubMed: 8985321
    32843: Mead JR, et al. In vitro expression of mRNA coding for a Cryptosporidium parvum oocyst wall protein. J. Eukaryot. Microbiol. 43: 84-85, 1996. PubMed: 8822876
    32899: von Dippe P, et al. The functional expression of sodium-dependent bile acid transport in Madin-Darby canine kidney cells transfected with the cDNA for microsomal epoxide hydrolase. J. Biol. Chem. 271: 18176-18180, 1996. PubMed: 8663355
    33046: Panneerselvam K, Freeze HH. Mannose enters mammalian cells using a specific transporter that is insensitive to glucose. J. Biol. Chem. 271: 9417-9421, 1996. PubMed: 8621609
    33080: Stuart RO, et al. Dependence of epithelial intercellular junction biogenesis on thapsigargin-sensitive intracellular calcium stores. J. Biol. Chem. 271: 13636-13641, 1996. PubMed: 8662885
    33127: Grindstaff KK, et al. Translational regulation of Na,K-ATPase alpha1 and beta1 polypeptide expression in epithelial cells. J. Biol. Chem. 271: 23211-23221, 1996. PubMed: 8798517

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    • MDCK细胞培养

      一、目的MDCK细胞培养是分离流感病毒及相关研究实验的基本技术。疾控中心的所有技术人员,必须按照本文件相关的操作规程进行操作。二、适用范围适用于疾控中心所有技术人员 。三、程序(一)生物安全要求实验室生物安全级别:BSL-1所有操作必须在BSL-1实验室的生物安全柜里进行。(二)材料1. 生长成片的MDCK细胞2. 无菌的T25细胞培养瓶3. D-MEM培养液(含有L-谷氨酰胺)4. 青、链霉素母液(10000 U/mL青霉素G;10000µg/mL硫酸链霉素),分装后保存于-20

    • 【求助】MDCK转染与免疫荧光问题,解决问题追加丁当,谢谢!

      wen-wen 实验组:将带有c-myc和UT-B的pcDNA3.0质粒转染到MDCK细胞当中 对照组:1、将带有c-Myc和AQP1的pcDNA3.0质粒转染到MDCK细胞; 2、将GFP的质粒(就是一个只有GFP的质粒,没有UT-B,AQP1)转染MDCK细胞中,主要目的是想看我的操作技术怎么样; 3、过表达AQP1-MDCK的稳转细胞系。 然后通过免疫荧光来证实转染结果。(因为质粒若带有GFP会影响

    • MDCK细胞培养SOP

      一、目的MDCK细胞培养是分离流感病毒及相关研究实验的基本技术。疾控中心的所有技术人员,必须按照本文件相关的操作规程进行操作。二、适用范围适用于疾控中心所有技术人员 。三、程序(一)生物安全要求实验室生物安全级别:BSL-1所有操作必须在BSL-1实验室的生物安全柜里进行。(二)材料1. 生长成片的MDCK细胞2. 无菌的T25细胞培养瓶3. D-MEM培养液(含有L-谷氨酰胺)4. 青、链霉素母液(10000 U/mL青霉素G;10000µg/mL硫酸链霉素),分装后保存于-20

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