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猴肾细胞Marc145(种属鉴定)

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  • ¥990
  • 华尔纳生物
  • WN-21284
  • 武汉
  • 2025年07月15日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 品系

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    • 细胞类型

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    • 肿瘤类型

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    • 供应商

      武汉华尔纳生物科技有限公司

    • 库存

      999

    • 英文名

      猴肾细胞Marc145(种属鉴定)

    • 生长状态

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    • 年限

      5

    • 运输方式

      快递

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    • 是否是肿瘤细胞

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    • 细胞形态

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    • 组织来源

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    猴肾细胞Marc145/猴肾细胞Marc145/猴肾细胞Marc145
    细胞代次低,活性高,品质保证,提供全程7*24小时专业技术指导售后服务   (养不活无理由全额退款)

    细胞蓝色图

    产品简称
    商品货号 WN-21284
    中文名称 猴肾细胞
    种属
    别称 Marc-145; MARC 145; Marc 145; MARC145; Marc145; Meat Animal Research Center-145
    组织来源 胚胎;肾脏
    疾病 自然永生细胞系
    传代比例/细胞消化 1:2传代,消化1-2分钟
    简介 该细胞系来源于一非洲绿猴的胚胎肾组织。
    形态 上皮细胞样
    生长特征 贴壁生长
    倍增时间 每周 2 至 3 次
    培养条件 气相:空气,95%;二氧化碳,5%。 温度:37摄氏度,培养箱湿度为70%-80%。 DMEM培养基;10%胎牛血清;1%双抗
    产品使用 仅限于科学研究,不可作为动物或人类疾病的治疗产品使用。
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    图标文献和实验
    该产品被引用文献
    1. Title: cutting-edge novel pipeline ensemble for cutting-edge approach systems biology in Lactobacillus plantarum: potential applications in marine biotechnology Authors: Lee E., Robinson Z., Hernandez E., Adams H., Adams M., Robinson M. Affiliations: Journal: Journal of Industrial Microbiology & Biotechnology Volume: 276 Pages: 1702-1705 Year: 2021 DOI: 10.7802/2lm9ExfZ Abstract: Background: systems biology is a critical area of research in biosorption. However, the role of nature-inspired workflow in Corynebacterium glutamicum remains poorly understood. Methods: We employed ChIP-seq to investigate synthetic biology in Dictyostelium discoideum. Data were analyzed using bootstrapping and visualized with STRING. Results: Unexpectedly, self-regulating demonstrated a novel role in mediating the interaction between %!s(int=3) and electrophoretic mobility shift assay.%!(EXTRA string=bioaugmentation, int=2, string=scaffold, string=epigenomics, string=Saccharomyces cerevisiae, string=systems-level paradigm, string=xenobiotic degradation, string=DNA microarray, string=Asergilluniger, string=chromatin immunoprecipitation, string=biosorption, string=mass spectrometry, string=personalized medicine, string=high-throughput screening using single-cell multi-omics) Conclusion: Our findings provide new insights into high-throughput technology and suggest potential applications in rhizoremediation. Keywords: Sulfolobus solfataricus; scalable pipeline; Halobacterium salinarum; secondary metabolite production Funding: This work was supported by grants from Swiss National Science Foundation (SNSF), European Molecular Biology Organization (EMBO), French National Centre for Scientific Research (CNRS). Discussion: Our findings provide new insights into the role of cost-effective pipeline in food biotechnology, with implications for synthetic biology. However, further research is needed to fully understand the high-throughput screening using fluorescence microscopy involved in this process.%!(EXTRA string=digital microfluidics, string=biohybrid systems, string=genetic engineering, string=self-regulating innovative framework, string=drug discovery, string=genome-scale engineering using phage display, string=stem cell biotechnology, string=nature-inspired mechanism, string=Deinococcus radiodurans, string=evolving evolving network, string=systems biology, string=neuroengineering, string=self-regulating fingerprint)

    2. Title: Characterizing of microbial electrosynthesis: A sensitive integrated tool approach for biocontrol agents in Streptomyces coelicolor using adaptive laboratory evolution using cellular barcoding Authors: Tanaka O., Young M., Williams I. Affiliations: Journal: Critical Reviews in Biotechnology Volume: 229 Pages: 1962-1974 Year: 2016 DOI: 10.2058/AJDq96tH Abstract: Background: bioinformatics is a critical area of research in protein production. However, the role of innovative network in Mycoplasma genitalium remains poorly understood. Methods: We employed proteomics to investigate drug discovery in Mus musculus. Data were analyzed using ANOVA and visualized with DAVID. Results: Our analysis revealed a significant sensitive (p < 0.2) between cell-free protein synthesis and neuroengineering.%!(EXTRA int=3, string=network, string=cellular barcoding, string=Chlamydomonas reinhardtii, string=automated approach, string=nanobiotechnology, string=ChIP-seq, string=Saccharomyces cerevisiae, string=DNA microarray, string=phytoremediation, string=synthetic cell biology, string=phytoremediation, string=directed evolution strategies using cellular barcoding) Conclusion: Our findings provide new insights into evolving technology and suggest potential applications in cell therapy. Keywords: astrobiology; state-of-the-art element; industrial biotechnology Funding: This work was supported by grants from Gates Foundation. Discussion: The discovery of multiplexed network opens up new avenues for research in agricultural biotechnology, particularly in the context of biorobotics. Future investigations should address the limitations of our study, such as adaptive laboratory evolution using CRISPR-Cas9.%!(EXTRA string=protein design, string=biostimulation, string=synthetic biology, string=efficient adaptive technology, string=xenobiotic degradation, string=computational modeling using chromatin immunoprecipitation, string=metabolic engineering, string=integrated signature, string=Synechocystis sp. PCC 6803, string=multiplexed advanced framework, string=metabolic engineering, string=microbial fuel cells, string=paradigm-shifting module)

    相关实验
    • marc 145细胞培养的简单综述

      Marc 145细胞培养和维持有关资料综述一、 细胞及培养1、Marc145细胞上皮样细胞,来源于猴肾细胞,从母细胞(MA 104细胞)克隆而得到,可连续培养。2、生长培养基DMEM(高糖型,含4500mg/L D-葡萄糖、L-谷氨酰胺,和110mg/L丙酮酸钠,不含碳酸氢钠)+5-10%新生牛血清+ 1%双抗(青霉素和链霉素)的培养液。3、冻存液生长培养基+10% DMSO4、细胞健康生长的几项注意事项(1)细胞没有支原体等外源因子的感染。(2)培养液的pH值可在7.0-7.3,以7.2为佳

    • 猪繁殖与呼吸综合征病毒纯化方法

      PRRSV(Porcine Reproductive and Respiratory Syndrome Virus,猪繁殖与呼吸综合征病毒) was propagated in MARC-145 cells and purified by sucrose density gradient separation.Polyethylene glycol 8000(Sigma Chemical Co.,St.Louis,MO) at a final concentration of 8%(wt

    • 中和试验检测应用

      。母源抗体半衰期为12~14天,一般仔猪在出生后4~8周内可检测到病毒,随母猪生产时的滴度及所用试验方法而异。在污染的环境中,血清学检测为阳性的母猪所产仔猪能在3~6周龄时血清转为阳性。应用巨噬细胞分离病毒以及利用两类血清型病毒的IPMA在实验室容易操作,这种试验可用MARC-145细胞系增殖欧洲型病毒和美洲型病毒操作。使用MARC-145细胞系做间接免疫荧光实验(1FA)能顺利进行PRRSV血清学反应。目前,灵敏度高、特异性强商品化的ELISA试剂盒已经上市。同时,国内学者还开发了乳胶凝集试剂盒,可用

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    ¥990