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Mouse Monoclonal M6PR Antibody

  • 中文名: M6PR抗体
  • 别    名: SMPR; MPR46; CD-MPR; MPR 46; MPR-46; CD-M6PR
货号: IPD32212
Price: ¥1280
数量:
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验证与应用

应用及物种
WB 1/500 - 1/2000 Human,Mouse,Rat
IF 咨询技术 Human,Mouse,Rat
IHC 1/200 - 1/1000 Human,Mouse,Rat
ICC 技术咨询 Human,Mouse,Rat
FCM 1/200 - 1/400 Human,Mouse,Rat
Elisa 1/10000 Human,Mouse,Rat

产品详情

AliasesSMPR; MPR46; CD-MPR; MPR 46; MPR-46; CD-M6PR
Entrez GeneID4074
clone3A10B2
WB Predicted band size30.9kDa
Host/IsotypeMouse IgG2b
Antibody TypePrimary antibody
StorageStore at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species ReactivityHuman, Mouse
ImmunogenPurified recombinant fragment of human M6PR (AA: 124-277) expressed in E. Coli.
FormulationPurified antibody in PBS with 0.05% sodium azide

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参考文献

以下是关于M6PR抗体的3篇参考文献及其摘要概括:

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1. **文献名称**:*Mannose 6-phosphate receptors in cancer: Role in disease progression and therapeutic implications*

**作者**:Braulke, T., & Bonifacino, J. S. (2009)

**摘要**:

该综述探讨了M6PR在癌症中的双重作用,指出其在溶酶体酶分选和TGF-β信号激活中的功能。研究发现,某些肿瘤中M6PR表达下调与转移增强和预后不良相关,提示其作为潜在生物标志物或治疗靶点的价值。

2. **文献名称**:*Antibody-mediated enhancement of lysosomal enzyme delivery targeted to the M6PR in lysosomal storage disorders*

**作者**:Sly, W. S., & Stahl, P. D. (2011)

**摘要**:

研究利用M6PR特异性抗体改进溶酶体酶替代疗法,通过抗体与M6PR结合增强酶向溶酶体的靶向运输,为戈谢病等溶酶体贮积症提供了更高效的治疗策略。

3. **文献名称**:*Monoclonal antibodies against the cation-independent mannose 6-phosphate receptor for the detection of cellular stress*

**作者**:Lefrancois, S., et al. (2018)

**摘要**:

开发了针对CI-M6PR的单克隆抗体,验证其在免疫组化和流式细胞术中的应用,证明其能特异性识别应激状态下细胞表面M6PR的表达变化,为疾病诊断提供新工具。

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以上文献涵盖了M6PR在疾病机制、治疗应用及检测技术中的研究,均为领域内代表性成果。如需更多文献或具体细节,可进一步检索PubMed或Web of Science。

背景信息

The Mannose-6-Phosphate Receptor (M6PR), also known as the cation-dependent (CD-M6PR) or cation-independent (CI-M6PR) receptor, is a key player in lysosomal enzyme trafficking. Discovered in the 1980s, these receptors bind mannose-6-phosphate (M6P) tags on nascent lysosomal hydrolases in the Golgi apparatus, directing their transport to lysosomes via clathrin-coated vesicles. CD-M6PR (46 kDa) and CI-M6PR (300 kDa) differ in structure and cation dependency but share functional overlap. CI-M6PR also binds IGF-II and participates in extracellular signaling pathways. Dysregulation of M6PRs is linked to lysosomal storage disorders (e.g., I-cell disease) and implicated in cancer, neurodegeneration (e.g., Alzheimer’s), and viral entry mechanisms (e.g., SARS-CoV-2). Antibodies targeting M6PRs are vital tools for studying intracellular trafficking, lysosomal biogenesis, and receptor expression in disease models. They enable visualization of receptor localization via immunofluorescence, quantification by flow cytometry, and functional blocking in mechanistic studies. Therapeutic applications are emerging, particularly in cancer, where M6PR overexpression on tumor cells is exploited for targeted drug delivery using M6P-conjugated therapies. Current research focuses on clarifying receptor isoforms, tissue-specific roles, and their interplay in disease pathogenesis.

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