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RKO-AS45-1人结肠癌转基因细胞(附STR鉴定报告)、

RKO-AS45-1细胞
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  • ¥1800
  • 南京万木春
  • 进口/国产
  • WM-23FN313
  • 2026年03月20日
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  • 企业认证

    • 详细信息
    • 文献和实验
    • 技术资料
    • 英文名

      RKO-AS45-1人结肠癌转基因细胞

    • 库存

      现货库存

    • 供应商

      南京万木春

    • 肿瘤类型

      RKO-AS45-1人结肠癌转基因细胞/

    • 细胞类型

      /

    • 品系

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    • 组织来源

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    • 相关疾病

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    • 物种来源

    • 免疫类型

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    • 细胞形态

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    • 是否是肿瘤细胞

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    • 器官来源

      /

    • 运输方式

      常温/干冰

    • 年限

      三代内

    • 生长状态

      /

    产品名称:RKO-AS45-1人结肠癌转基因细胞、RKO-AS45-1人结肠癌转基因细胞、RKO-AS45-1人结肠癌转基因细胞、RKO-AS45-1人结肠癌转基因细胞;

     
     


    A variety of cutting-edge methods and good knowledge of the illnesss complex causes are causing a sea change in the field of Alzheimers Disease (A.D.) research and treatment. Precision medicine is at the vanguard of this change, where individualized treatment plans based on genetic and biomarker profiles give a ray of hope for customized therapeutics. Combination therapies are becoming increasingly popular as a way to address the multifaceted pathology of Alzheimers by simultaneously attacking Aβ plaques, tau tangles, neuroinflammation, and other factors. The article covers several therapeutic design efforts, including BACE inhibitors, gamma- secretase modulators, monoclonal antibodies (e.g., Aducanumab and Lecanemab), and anti- Aβ vaccinations. While these techniques appear promising, clinical development faces safety concerns and uneven efficacy. To address the complicated Aβ pathology in Alzheimers disease, a multimodal approach is necessary. The statement emphasizes the continued importance of clinical trials in addressing safety and efficacy concerns. Looking ahead, it suggests that future treatments may take into account genetic and biomarker traits in order to provide more personalized care. Therapies targeting Aβ, tau tangles, neuroinflammation, and novel drug delivery modalities are planned. Nanoparticles and gene therapies are only two examples of novel drug delivery methods that have the potential to deliver treatments more effectively, 

    to be a driving force in many cancers as exemplified in patients with inflammatory bowel disease that have an increased risk of colorectal cancer. Indeed, NKT cells promote intestinal inflammation in human ulcerative colitis, and the associated animal model, indicating that NKT

    nodes (MLNs) and TDLNs, diminished DC and effector CD8+ T cell responses, and attenuated responses to ICT.
     


     

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    图标文献和实验
    该产品被引用文献

    RKO-AS45-1人结肠癌转基因细胞cells may favor tumor development in intestinal tissue. In contrast to other cancers, recent data

    相关实验
    • 【求助】关于结肠癌细胞

      CRL-2578 Homo sapiens (human) RKO-E6 CRL-2579 Homo sapiens (human) RKO-AS45-1 CRL-2780 Homo sapiens (human) ATRFLOX [Mutatect] CRL-5972 Homo sapiens (human) SNU-C1 CRL-7213 Homo sapiens (human) Hs 255.T CRL-7214 Homo sapiens (human

    • 细胞名称大汇总

      -N87         人胃癌细胞 3、鸟 类 DT40          鸡淋巴瘤细胞 三、工程细胞RKO-E6         人结肠癌转基因细胞    RKO-AS45-1      人结肠癌转基因细胞 PK136          抗小鼠 NK        细胞的杂交瘤细胞 PC 61 5.3        杂交瘤细胞 四、干细胞系 ES-D3(CRL-1934)     小鼠胚胎干细胞      ES-D3(CRL-11632)   小鼠胚胎干细胞

    • 中国科学院细胞库可供应细胞目录

      肝癌细胞  400元 RKO  TCHu116  人  结肠腺癌细胞  1000元 RKO-AS45-1  TCHu117  人  结肠癌转基因细胞  1000元 RKO-E6  TCHu118  人  结肠癌转基因细胞  1000元 RM-1  TCM14  小鼠  前列腺癌细胞  400元 S-180  TCM15  小鼠  腹水瘤细胞  400元 SAC-ⅡB2  TCM16  小鼠  腹水瘤细胞  400元 SAC-ⅡC3  TCM17  小鼠  腹水瘤细胞  400元

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    文献支持
    RKO-AS45-1人结肠癌转基因细胞(附STR鉴定报告)、RKO-AS45-1细胞
    ¥1800