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        RWPE-2 人前列腺正常細胞

        • 更新時間:  2020-10-15
        • 產品型號:  CRL-11610
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        • CRL-11610 RWPE-2 人前列腺正常細胞,原代細胞|細胞系|細胞株|菌種;細胞庫管理規范,提供的細胞株背景清楚,提供參考文獻和Z優培養條件!

        CRL-11610 RWPE-2 人前列腺正常細胞

        ATCC® Number:CRL-11610™    Price: 
        Depositors: Michigan State University, National Cancer Institute
        Biosafety Level:2 [Cells contain Human Papilloma viral (HPV) sequences ]
        Medium & Serum:See Propagation
        Growth Properties:adherent
        Organism:Homo sapiens (human)
        Morphology:CRL-11610 RWPE-2 人前列腺正常細胞epithelial
        Source:Organ: prostate 
        Disease: normal 
        Cell Type: epithelial
        Cellular Products:cytokeratin 18 [46793] 
        cytokeratin 8 [46793]
        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 ultimay responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.
        Receptors:androgen receptor, expressed ( [46793] upregulated upon exposure to androgen)
        Antigen Expression:kallikrein 3, KLK3 (prostate specific antigen, PSA); Homo sapiens, expressed (upon exposure to androgen) ( [46793] upon exposure to androgen)
        DNA Profile (STR):Amelogenin: X,Y 
        CSF1PO: 13 
        D13S317: 8,14 
        D16S539: 9,11 
        D5S818: 12,15 
        D7S820: 10,11 
        THO1: 8,9.3 
        TPOX: 8,11 
        vWA: 14,18
        Cytogenetic Analysis:At passage 14, a majority of the cells were in the near diploid range (48-54), with the main population being 51, XY. [46795]
        Isoenzymes:AK-1, 1 
        ES-D, 2 
        G6PD, B 
        GLO-I, 1-2 
        Me-2, 0 
        PGM1, 2 
        PGM3, 1
        Gender:CRL-11610 male
        Ethnicity:Caucasian, White
        Comments:Tumor Suppressor Gene(s):pRB + [PubMed: 9214605]
        RWPE-2 cells were derived from RWPE-1 cells (ATCC CRL-11609) by transformation with Ki-ras using the Kirsten murine sarcoma virus (Ki-MuSV) [PubMed: 9214605]. Epithelial cells from the peripheral zone of a histologically normal adult human prostate were transfected with a plasmid carrying one copy of the human papilloma virus 18 (HPV-18) genome to establish the RWPE-1 cell line (ATCC CRL-11609). RWPE-1 cells neither grow in agar nor form tumors when injected into nude mice with or without Matrigel. However, RWPE-2 cells form small colonies in soft agar and form tumors when injected into nude mice [PubMed: 9214605]. Further, a family of tumorigenic cell lines, that mimics multiple steps in prostate cancer progression, was also derived from RWPE-1 cells by exposure to N-methyl-N-nitrsourea (MNU). See the WPE1-NA22 (ATCCCRL-2849), WPE1-NB14 (ATCC CRL-2850), WPE1-NB11 (ATCC CRL-2851) and WPE1-NB26 (ATCC CRL-2852) cell ines.
        The depositor reports that the RWPE-1 cell line (ATCC CRL-11609) was screened, and found negative for, Hepatitis B virus, Hepatitis C virus and Human immunodeficiency virus.
        Propagation:ATCC complete growth medium: The base medium for this cell line is provided by Invitrogen (GIBCO) as part of a kit: Keratinocyte Serum Free Medium (K-SFM), Kit Catalog Number 17005-042. This kit is supplied with each of the two additives required to grow this cell line (bovine pituitary extract (BPE) and human recombinant epidermal growth factor (EGF). To make the complete growth medium, you will need to add the following components to the base medium:
        • 0.05 mg/ml BPE - provided with the K-SFM kit
        • 5 ng/ml EGF - provided with the K-SFM kit. NOTE: Do not filter complete medium. 
          Atmosphere: air, 95%; carbon dioxide (CO2), 5% 
          Temperature: 37.0°C
        Subculturing:CRL-11610 Protocol:
        1. Remove and discard culture medium.
        2. Briefly rinse the cell layer with Ca++/Mg++ free Dulbecco's phosphate-buffered saline (D-PBS).
        3. Add 2.0 to 3.0 ml (to a T-25 flask) or 3.0 to 4.0 ml (to a T-75 flask) of 0.05% Trypsin - 0.53mM EDTA solution, diluted 1:1 with D-PBS, and place flask in a 37C incubator for 5 to 8 minutes. Observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 10 minutes).
          Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach.
        4. Add 6.0 to 8.0 ml of 0.1% Soybean Trypsin Inhibitor (or 2% fetal bovine serum in D-PBS), as appropriate, and aspirate cells by gently pipetting.
        5. Transfer cell suspension to centrifuge tube and spin at approximay 125 x g for 5 to 7 minutes.
        6. Discard supernatant and resuspend cells in fresh serum-free growth medium. Add appropriate aliquots of cell suspension to new culture vessels. An inoculum of 2 X 10(4) to 4 X 10(4) viable cells/sq. cm is recommended.
        7. Incubate cultures at 37C. We recommend that you maintain cultures at a cell concentration between 4 X 10(4) and 8 X 10(4) cells/sq. cm.
        Cells grown under serum-free or reduced serum conditions may not attach strongly during the 24 hours after subculture and should be disturbed as little as possible during that period. 
        Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:5 is recommended 
        Medium Renewal: Every 2 days
        Preservation:Freeze medium: Complete growth medium supplemented with 10% (v/v) DMSO 
        Storage temperature: liquid nitrogen vapor phase
        Related Products:parental cell line:ATCC CRL-11609
        purified DNA:ATCC CRL-11610D
        derived from same individual:ATCC CRL-2849
        derived from same individual:ATCC CRL-2850
        derived from same individual:ATCC CRL-2852
        derived from same individual:ATCC CRL-2851
        derivative:ATCC CRL-2853
        derived from same individual:ATCC CRL-2854
        References:46792: Webber MM, Rhim JS. Immortalized and malignant human prostatic cell lines. US Patent 5,824,488 dated Oct 20 1998
        46793: Bello D, et al. Androgen responsive adult human prostatic epithelial cell lines immortalized by human papillomavirus 18. Carcinogenesis 18: 1215-1223, 1997. PubMed: 9214605
        46795: Webber MM, et al. Acinar differentiation by non-malignant immortalized human prostatic epithelial cells and its loss by malignant cells. Carcinogenesis 18: 1225-1231, 1997. PubMed: 9214606
        53180: Webber MM, et al. Immortalized and tumorigenic adult human prostatic epithelial cell lines: characteristics and applications. Part I. Cell markers and immortalized nontumorigenic cell lines. Prostate 29: 386-394, 1996. PubMed: 8977636
        53181: Webber MM, et al. Immortalized and tumorigenic adult human prostatic epithelial cell lines: characteristics and applications Part 2. Tumorigenic cell lines. Prostate 30: 58-64, 1997. PubMed: 9018337
        53182: Webber MM, et al. Immortalized and tumorigenic adult human prostatic epithelial cell lines: characteristics and applications. Part 3. Oncogenes, suppressor genes, and applications. Prostate 30: 136-142, 1997. PubMed: 9051152
        53183: Kremer R, et al. ras Activation of human prostate epithelial cells induces overexpression of parathyroid hormone-related peptide. Clin. Cancer Res. 3: 855-859, 1997. PubMed: 9815759
        53192: Jacob K, et al. Osteonectin promotes prostate cancer cell migration and invasion: a possible mechanism for metastasis to bone. Cancer Res. 59: 4453-4457, 1999. PubMed: 10485497


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