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InVivoMAb anti-human PD-1 (CD2

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  • ¥4000 - 24000
  • biocell
  • BE0188
  • 2026年05月28日
    • 详细信息
    • 文献和实验
    • 技术资料
    • 亚型

      J116

    • 克隆性

      单克隆

    • 抗体英文名

      InVivoMAb anti-human PD-1 (CD279)

    • 规格

      mg

    InVivoMAb anti-human PD-1 (CD279)
    Isotype
    The J116 monoclonal antibody reacts with human PD-1 (programmed death-1) also known as CD279. PD-1 is a 50-55 kDa cell surface receptor encoded by the Pdcd1 gene that belongs to the CD28 family of the Ig superfamily. PD-1 is transiently expressed on CD4 and CD8 thymocytes as well as activated T and B lymphocytes and myeloid cells. PD-1 expression declines after successful elimination of antigen. Additionally, Pdcd1 mRNA is expressed in developing B lymphocytes during the pro-B-cell stage. PD-1's structure includes a ITIM (immunoreceptor tyrosine-based inhibitory motif) suggesting that PD-1 negatively regulates TCR signals. PD-1 signals via binding its two ligands, PD-L1 and PD-L2 both members of the B7 family. Upon ligand binding, PD-1 signaling inhibits T-cell activation, leading to reduced proliferation, cytokine production, and T cell death. Additionally, PD-1 is known to play key roles in peripheral tolerance and prevention of autoimmune disease in mice as PD-1 knockout animals show dilated cardiomyopathy, splenomegaly, and loss of peripheral tolerance. Induced PD-L1 expression is common in many tumors including squamous cell carcinoma, colon adenocarcinoma, and breast adenocarcinoma. PD-L1 overexpression results in increased resistance of tumor cells to CD8 T cell mediated lysis. In mouse models of melanoma, tumor growth can be transiently arrested via treatment with antibodies which block the interaction between PD-L1 and its receptor PD-1. For these reasons anti-PD-1 mediated immunotherapies are currently being explored as cancer treatments. Binding of the J116 antibody is reported to inhibit PD-1 signal transduction, however, it is not reported to block PD-L1 binding.
    InVivoMAb anti-human PD-1 (CD279)
    Clone Catalog # Category
    J116 BE0188 InVivoMab Antibodies
     

    Mouse IgG1

    Recomended Isotype Control(s) InVivoMAb mouse IgG1 isotype control, unknown specificity
    Recommended InVivoPure Dilution Buffer InVivoPure pH 7.0 Dilution Buffer
    Immunogen

    Not available or unknown

    Reported Applications
    • in vitro PD-1 neutralization
    • in vivo PD-1 blockade in humanized mice
    Endotoxin
    • <2EU/mg (<0.002EU/μg)
    • Determined by LAL gel clotting assay
    Purity
    • >95%
    • Determined by SDS-PAGE
    Formulation
    • PBS, pH 7.0
    • Contains no stabilizers or preservatives
    Sterility

    0.2 μM filtered

    Production

    Purified from tissue culture supernatant in an animal free facility

    Purification

    Protein G

    Storage

    Undiluted at 4°C in the dark

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    图标文献和实验
    相关实验
    • 不只是 PD-1CD96 正成为免疫治疗的下一个“必争之地”

      , Markus Mezger.(2023). CRISPR-Cas9-Based Gene Knockout of Immune Checkpoints in Expanded NK Cells. [14] Chelsia Qiuxia Wang, F. C. Choy, A. Sanny, Takashi Murakami, A. Tan, K. Lam.(2023). An Inhibitory Role for Human CD96 Endodomain in T Cell Anti-Tumor

    • 这种水果将助力癌症治疗?增强免疫治疗效果,有望克服 PD-1 耐药难题!

      素 C、花青素类物质,已被证明可以通过增加肠道中嗜粘液杆菌(A.muciniphila)和双歧杆菌(Bifidobacterium)的丰度,对小鼠的肥胖和相关代谢紊乱发挥保护性作用。 2022 年 1 月 14 日,来自加拿大蒙特利尔大学研究中心的 Bertrand Routy 团队在 Cancer Discovery 上发表了题为 A natural polyphenol exerts antitumor activity and circumvents anti-PD-1 resistance

    • 一年内两次叫停!康方CD73单抗又“悬”了,PD-1的黄金搭档还香吗?

      肿瘤免疫治疗中,PD-1/L1抑制剂单药响应率有限,寻找“黄金搭档”成为焦点。CD73曾被视为最具潜力的免疫代谢靶点之一——它通过催化产生腺苷,在肿瘤微环境中形成免疫抑制屏障,阻断CD73有望“解放”T细胞,与PD-1联用实现增效。 然而理想丰满,现实骨感。2026年3月11日,外媒报道康方生物暂停了CD73单抗(drebuxelimab)联合依沃西单抗治疗非小细胞肺癌的Ib/II期研究(AK119-201),官方称“研发战略优先级调整”。这已是康方第二次叫停CD73相关试验——2025年2月

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