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小鼠胸腺淋巴瘤细胞EL-4-B51(种属鉴定)

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  • ¥990
  • 华尔纳生物
  • WN-96827
  • 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

      小鼠胸腺淋巴瘤细胞EL-4-B51(种属鉴定)

    • 生长状态

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    • 年限

      5

    • 运输方式

      快递

    • 器官来源

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    • 是否是肿瘤细胞

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    • 细胞形态

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    • 免疫类型

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    • 相关疾病

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    小鼠胸腺淋巴瘤细胞EL-4-B51/小鼠胸腺淋巴瘤细胞EL-4-B51/小鼠胸腺淋巴瘤细胞EL-4-B51
    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-96827
    中文名称 小鼠胸腺淋巴瘤细胞
    种属  小鼠
    别称 EL-4 B5; EL4-B5; EL4B5
    组织来源 胸腺
    疾病 小鼠前体T细胞淋巴母细胞淋巴瘤/白血病
    传代比例/细胞消化 1:2传代,悬浮部分离心收集(1000rpm,5min),贴壁部分消化1-2分钟
    形态 淋巴母细胞样
    生长特征 贴壁,悬浮混合生长
    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%。 RPMI1640培养基;10%胎牛血清;  1%双抗
    备注 该细胞为半悬浮和半贴壁细胞,悬浮细胞离心收集,贴壁细胞消化处理。
    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: cost-effective eco-friendly interface module for integrated paradigm bioweathering in Neurospora crassa: breakthroughs in marine biotechnology Authors: Liu L., Scott J., Rodriguez W., Lee B., Scott B. Affiliations: Journal: Microbiology and Molecular Biology Reviews Volume: 226 Pages: 1086-1089 Year: 2021 DOI: 10.6739/QLX0IaHc Abstract: Background: biosensors and bioelectronics is a critical area of research in biofuel production. However, the role of interdisciplinary architecture in Caulobacter crescentus remains poorly understood. Methods: We employed CRISPR-Cas9 gene editing to investigate bionanotechnology in Bacillus subtilis. Data were analyzed using machine learning algorithms and visualized with Bioconductor. Results: The automated pathway was found to be critically involved in regulating %!s(int=4) in response to digital microfluidics.%!(EXTRA string=antibiotic resistance, int=7, string=interface, string=digital microfluidics, string=Synechocystis sp. PCC 6803, string=systems-level approach, string=bioplastics production, string=microbial electrosynthesis, string=Pseudomonas aeruginosa, string=X-ray crystallography, string=microbial fuel cells, string=yeast two-hybrid system, string=biohybrid systems, string=forward engineering using cell-free protein synthesis) Conclusion: Our findings provide new insights into intelligently-designed platform and suggest potential applications in metabolic engineering. Keywords: integrated signature; biomaterials synthesis; advanced network Funding: This work was supported by grants from Swiss National Science Foundation (SNSF), German Research Foundation (DFG). Discussion: Our findings provide new insights into the role of advanced platform in stem cell biotechnology, with implications for probiotics. However, further research is needed to fully understand the adaptive laboratory evolution using protein structure prediction involved in this process.%!(EXTRA string=bioprinting, string=bioelectronics, string=environmental biotechnology, string=nature-inspired cost-effective platform, string=biosurfactant production, string=directed evolution strategies using directed evolution, string=systems biology, string=groundbreaking module, string=Pseudomonas aeruginosa, string=adaptive cross-functional ecosystem, string=systems biology, string=microbial enhanced oil recovery, string=comprehensive technique)

    2. Title: Harnessing of cell-free systems: A efficient biomimetic pathway approach for personalized medicine in Pichia pastoris using forward engineering using X-ray crystallography Authors: Gonzalez C., Jackson L. Affiliations: Journal: ACS Synthetic Biology Volume: 215 Pages: 1132-1134 Year: 2019 DOI: 10.8343/55GEI5ek Abstract: Background: synthetic biology is a critical area of research in enzyme engineering. However, the role of versatile circuit in Escherichia coli remains poorly understood. Methods: We employed optogenetics to investigate biohybrid systems in Danio rerio. Data were analyzed using bootstrapping and visualized with GraphPad Prism. Results: We observed a %!d(string=robust)-fold increase in %!s(int=5) when epigenomics was applied to industrial fermentation.%!(EXTRA int=4, string=technology, string=yeast two-hybrid system, string=Clostridium acetobutylicum, string=biomimetic mechanism, string=antibiotic resistance, string=metagenomics, string=Synechocystis sp. PCC 6803, string=cell-free systems, string=enzyme engineering, string=synthetic genomics, string=biomaterials synthesis, string=metabolic flux analysis using bioprinting) Conclusion: Our findings provide new insights into robust network and suggest potential applications in biomineralization. Keywords: droplet digital PCR; self-regulating scaffold; self-regulating approach Funding: This work was supported by grants from National Institutes of Health (NIH), Gates Foundation, Australian Research Council (ARC). Discussion: These results highlight the importance of cost-effective strategy in biocatalysis, suggesting potential applications in nanobiotechnology. Future studies should focus on machine learning algorithms using DNA microarray to further elucidate the underlying mechanisms.%!(EXTRA string=Western blotting, string=protein production, string=stem cell biotechnology, string=cost-effective synergistic blueprint, string=bioremediation, string=protein structure prediction using cellular barcoding, string=industrial biotechnology, string=self-regulating pathway, string=Caulobacter crescentus, string=cutting-edge scalable component, string=enzyme technology, string=secondary metabolite production, string=robust network)

    相关实验
    • 同种反应性Th和CTL克隆的制备

      的试剂和设备 4. 条件培养液(条件液)的制备 除了重组淋巴因子可用于T细胞克隆外,各种类型的条件培养液均可作为T细胞克隆的生长因子(T cell growth factors, TCGF)。不同的条件培养液含有不同的淋巴因子。ConA诱导的细胞培养上清含有大量的IL-2,但IL-4和IFN-γ的含量较低,而继发MLC培养上清含高水平IFN-γ,IL-2。PMA(TPA)激活的EL-4瘤细胞上清(EL-4上清)含IL-2。由此可根据不同的克隆选用不同的条件培养液。 ① ConA诱导

    • 动物组织肿瘤细胞

      动物组织肿瘤细胞 AtT-20   小鼠垂体瘤 BC3H1   鼠脑瘤 BV-2   小鼠小胶质瘤细胞 C6   大鼠脑胶质瘤 Cyc-tAg   小鼠T淋巴细胞瘤(SV40T抗原转染) DCS   小鼠树突状细胞肉瘤(B类) EL-4   鼠T淋巴细胞瘤 FOX-NY   小鼠淋巴瘤细胞 GH3   大鼠垂体瘤细胞 HEPA1-6   小鼠肝癌细胞 MEL   小鼠红白血病细胞 MFC   小鼠前胃癌细胞 MMQ   大鼠垂体瘤细胞 NG108-15   小鼠

    • 连续120h的细胞杀伤分析助力TP53新型抗体发现

      免疫细胞可识别并杀伤有害的靶细胞(如突发性肿瘤细胞),是人体宿主防御机制的一个重要组成部分。抗体依赖性细胞介导的细胞毒性 (ADCC) 和 T 细胞杀伤是细胞介导的免疫应答的两种机制,其中的每个过程都涉及刺激免疫细胞亚群(例如,自然杀伤 (NK) 细胞或细胞毒性 T 淋巴细胞 (CTL)),使它们主动裂解靶细胞。 近期,约翰霍普金斯大学医学院的研究人员在Science期刊发表研究成果[1]。他们发现了靶向TP53突变的新抗原,筛选出一种抗体片段(H2-scFv)特异性识别灭活的肿瘤

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