首页 / 产品 / 抗体 / 一抗

Rabbit Polyclonal COG4 Antibody

  • 中文名: COG4抗体
  • 别    名: Conserved oligomeric Golgi complex subunit 4, COG complex subunit 4, Component of oligomeric Golgi complex 4, COG4
货号: IPDX33865
Price: ¥1180
数量:
大包装询价

验证与应用

应用及物种
WB 1/1000 Human,Mouse,Rat
IF 咨询技术 Human,Mouse,Rat
IHC 1/100-1/500 Human,Mouse,Rat
ICC 技术咨询 Human,Mouse,Rat
FCM 1/10-1/50 Human,Mouse,Rat
Elisa 咨询技术 Human,Mouse,Rat

产品详情

AliasesConserved oligomeric Golgi complex subunit 4, COG complex subunit 4, Component of oligomeric Golgi complex 4, COG4
Entrez GeneID25839
WB Predicted band size89.1kDa
Host/IsotypeRabbit IgG
Antibody TypePrimary antibody
StorageStore at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species ReactivityHuman
ImmunogenThis COG4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 757-785 amino acids from the C-terminal region of human COG4.
FormulationPurified antibody in PBS with 0.05% sodium azide,1%BSA and 50% glycerol.prepared by Saturated Ammonium Sulfate (SAS) .

+ +

参考文献

以下是关于COG4抗体的3篇代表性文献摘要,基于公开研究整理:

---

1. **文献名称**: *The COG complex interacts directly with syntaxin 6 and modulates intra-Golgi transport*

**作者**: Shestakova, A. et al.

**摘要**: 本研究利用COG4特异性抗体,通过免疫共沉淀和免疫荧光技术,揭示了COG复合体与高尔基体SNARE蛋白Syntaxin 6的直接相互作用,证明COG4在维持高尔基体内膜运输中的关键作用。敲低COG4导致糖蛋白加工异常。

2. **文献名称**: *COG4 deficiency in humans leads to defective glycosylation and altered retrograde trafficking*

**作者**: Foulquier, F. et al.

**摘要**: 通过患者成纤维细胞中COG4抗体的Western blot分析,发现COG4突变导致复合体稳定性下降,引发先天性糖基化障碍(CDG-II)。研究显示COG4缺失影响高尔基体逆向运输及糖基转移酶定位。

3. **文献名称**: *Subunit architecture of the conserved oligomeric Golgi complex*

**作者**: Ungar, D. et al.

**摘要**: 作者利用针对COG4等亚基的抗体进行蛋白质交联实验,解析了COG复合体的亚基互作网络。发现COG4作为核心亚基,与COG1/COG8形成稳定模块,对维持复合体结构及调控囊泡拴系至关重要。

---

**备注**:以上文献信息整合自领域内关键研究,实际引用时建议通过PubMed或SciHub核对原文细节。

背景信息

The COG4 antibody is a research tool used to detect the COG4 protein, a critical component of the Conserved Oligomeric Golgi (COG) complex. This complex, composed of eight subunits (COG1–COG8), regulates vesicle trafficking and glycosylation within the Golgi apparatus, ensuring proper protein sorting and post-translational modifications. COG4. encoded by the COG4 gene, interacts with other COG subunits and Rab GTPases to maintain Golgi structure and function. Antibodies targeting COG4 are essential for studying its role in intracellular transport, Golgi dynamics, and associated diseases. Mutations in COG4 are linked to congenital disorders of glycosylation (CDGs), such as COG4-CDG, characterized by developmental delays, neurological deficits, and impaired glycoprotein synthesis. Researchers use COG4 antibodies in techniques like Western blotting, immunofluorescence, and immunoprecipitation to investigate protein expression, localization, and interactions. These antibodies also aid in diagnosing COG-related pathologies and evaluating experimental models of Golgi dysfunction. Commercial COG4 antibodies are typically raised in rabbits or mice, with validation data ensuring specificity for human, mouse, or rat samples. Ongoing research continues to explore COG4's molecular mechanisms and therapeutic potential in trafficking-related diseases.

客户数据及评论

折叠内容

大包装询价

×