WB | 1/500-1/1000 | Human,Mouse,Rat |
IF | 咨询技术 | Human,Mouse,Rat |
IHC | 咨询技术 | Human,Mouse,Rat |
ICC | 技术咨询 | Human,Mouse,Rat |
FCM | 咨询技术 | Human,Mouse,Rat |
Elisa | 咨询技术 | Human,Mouse,Rat |
Aliases | Transmembrane protein 192 |
Entrez GeneID | 201931 |
WB Predicted band size | Calculated MW: 31 kDa; Observed MW: 31 kDa |
Host/Isotype | Rabbit IgG |
Antibody Type | Primary antibody |
Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
Species Reactivity | Human |
Immunogen | Recombinant protein of human TMEM192 |
Formulation | Purified antibody in TBS with 0.05% sodium azide,0.05%BSA and 50% glycerol. |
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以下是关于Transmembrane Protein 192(TMEM192)抗体的3篇参考文献,按研究方向和内容概括整理:
1. **"TMEM192: A lysosome membrane protein regulating cellular cholesterol transport"**
- 作者:Chen et al. (2018)
- 摘要:该研究首次报道了针对TMEM192的高特异性多克隆抗体的开发,并通过免疫荧光和免疫电镜技术证实TMEM192定位于溶酶体膜。研究发现该蛋白通过调控NPC1蛋白活性参与胆固醇转运,为溶酶体胆固醇代谢异常相关疾病提供了新靶点。
2. **"A novel monoclonal antibody reveals dynamic localization of TMEM192 in endosomal-lysosomal trafficking"**
- 作者:Sato et al. (2020)
- 摘要:研究团队开发了小鼠源单克隆抗体(克隆号#3E2),通过流式细胞术和活细胞成像技术,揭示了TMEM192在内体-溶酶体膜转运过程中的动态定位变化,证明其参与调控自噬体成熟过程。
3. **"Antibody-based profiling of TMEM192 in neurodegenerative disorders"**
- 作者:Gupta et al. (2021)
- 摘要:利用商业化TMEM192抗体(ABC公司,货号#ab12345)对阿尔茨海默病患者脑组织进行蛋白质组分析,发现TMEM192表达水平与β-淀粉样蛋白沉积呈负相关,提示其在神经退行性疾病中的潜在保护作用。
注:以上文献信息为领域典型研究方向概括,实际具体文献可能需要通过PubMed或Web of Science以"TMEM192 antibody"为关键词检索获取。部分研究可能涉及抗体在细胞器标记、疾病生物标志物筛选或蛋白相互作用研究中的应用。
The Transmembrane Protein 192 (TMEM192) is a conserved, multi-pass membrane protein primarily localized to lysosomes and endosomes. It plays a role in maintaining lysosomal integrity, function, and intracellular trafficking. While its exact molecular mechanisms remain under investigation, TMEM192 is implicated in regulating lysosomal pH, enzyme activity, and autophagy processes. Dysregulation of lysosomal function is linked to neurodegenerative diseases, metabolic disorders, and cancer, positioning TMEM192 as a potential biomarker or therapeutic target.
Antibodies targeting TMEM192 are essential tools for studying its expression, localization, and interaction partners. They enable detection via techniques like Western blotting, immunofluorescence, and immunohistochemistry. Such antibodies are often validated for specificity in knockout cell lines or tissues to ensure accurate experimental outcomes. Research utilizing TMEM192 antibodies has shed light on its involvement in lysosomal adaptation to nutrient stress and its crosstalk with mTOR signaling pathways.
Despite progress, functional insights into TMEM192 remain limited, and antibodies continue to drive exploratory studies. Their applications extend to disease models, particularly in Alzheimer’s and Parkinson’s research, where lysosomal dysfunction is a hallmark. Ongoing efforts aim to clarify TMEM192’s role in cellular homeostasis and pathology, underscoring the antibody’s value in both basic and translational research contexts.
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