Anti-VE Cadherin antibody - Intercellular Junction Marker (Ab33168)

CD144, Cadherin-5, 7B4 antigen, Vascular endothelial cadherin, VE-cadherin, CDH5

反应种属:Human, Mouse
抗原名称:Cdh5
应用:WB, IF/ICC

详细信息

免疫原The exact immunogen used to generate this antibody is proprietary information.
宿主/亚型Rabbit / IgG
抗体类型Polyclonal
产品形式Liquid
纯化方式Affinity purification Immunogen
储存缓冲液pH: 7.4 Preservative: 0.02% Sodium azide Constituents: PBS, 1% BSA
储存条件运输条件: Blue Ice 推荐的短期储存时间: 1-2 weeks 推荐的短期储存条件: +4°C 推荐的长期储存条件: -20°C 储存信息: Avoid freeze / thaw cycle
无载体蛋白No

特异性

From May 2024, QC testing of replenishment batches of this polyclonal changed. All tested and expected application and reactive species combinations are still covered by our Abcam product promise. However, we no longer test all applications. For more information on a specific batch, please contact our Scientific Support who will be happy to help.

背景信息

Anti-VE Cadherin antibody - Intercellular Junction Marker (ab33168) is a rabbit polyclonal antibody and is validated for use in ICC/IF, WB in mouse, rat samples. Anti-VE Cadherin antibody - Intercellular Junction Marker (ab33168) has been cited over 361 times in peer reviewed journals and is trusted by the scientific community. Abcam's high quality validation processes ensure Anti-VE Cadherin antibody - Intercellular Junction Marker (ab33168) has high sensitivity and specificity. Anti-VE Cadherin antibody - Intercellular Junction Marker (ab33168) has 39 independent reviews from customers. Anti-VE Cadherin antibody - Intercellular Junction Marker (ab33168) specifically detects VE Cadherin (UniProt ID: P33151; Molecular weight: 83kDa) and is sold in 100 µg selling sizes.

文献引用 (450)

Deployable 3D-Printed Vascular Stent with Surface-Catalysed Endogenous Nitric Oxide Generation.

可部署的 3D 打印血管支架,具有表面催化内源性一氧化氮生成功能。

Zhou Kun, Han Zifei, Lin Kang, Wu Di, Adzlan Siti Nur Asyura, Fan Qingqing, Cortez-Jugo Christina, Chandrawati Rona, Boyer Cyrille

Synergistic fusion of CD47, VE-cadherin and mussel adhesion protein promotes endothelialization and suppresses inflammation in vascular stents.

CD47、VE-钙黏蛋白和贻贝黏附蛋白的协同融合可促进血管支架内皮化并抑制炎症。

Yan Wenhua, Li Shuyu, Zhang Tian, Huang Junli, Deng Chengchen, Yuan Kunshan, Huang Nan, Zhang Haijun, Wang Guixue

Vascular Endothelial Growth Factor-D Improves Lung Vascular Integrity During Acute Lung Injury.

血管内皮生长因子-D可改善急性肺损伤期间的肺血管完整性。

Yoon Yongdae, Sharma Lokesh, Tang Wenwen, Kirk Shannon, Raredon Micha Sam Brickman, Ahangari Farida, Khoury Johad, Qian Hong, Ke Yunbo, Tulapurkar Mohan, Liu Ruya, Luan Yi, Yuan Qianying, Chen Lujia, Birukov Konstantin, Simons Michael, Wu Dianqing, Niklason Laura E, Kaminski Naftali, Yuan Yifan

FGF 13 functions as a regulator of the ERK/aerobic glycolysis axis in the inflammatory state during septic lung injury.

FGF 13 在脓毒症肺损伤的炎症状态下,作为 ERK/有氧糖酵解轴的调节因子发挥作用。

Zhu Junjie, Wang Jiaqi, Jiang Chunhui, Wang Jie, Zhou Jie, Tong Gaozan, Wu Yuecheng, Ou Zhuoyao, Ye Junbo, Shen Enzhao, Ke Anqi, Li Fan, Jiang Meifan, Ma Jihong, Jin Litai, Li Xiaokun, Cong Weitao

Activator protein-1 (AP-1) inhibition prevents endothelial to mesenchymal transition in diabetes-associated atherosclerosis: a translational study.

激活蛋白-1 (AP-1) 抑制可预防糖尿病相关动脉粥样硬化中的内皮细胞向间质细胞转化:一项转化研究。

Khan Abdul Waheed, Aziz Misbah, Sourris Karly C, Cortes Jairo P, Block Tomasz J, Dai Aozhi, Maxwell Scott, Okabe Jun, Pyper Emma, Paneni Francesco, Cooper Mark E, Jandeleit-Dahm Karin Am

Lysolecithin reprogramming via LPCAT1 modulation restores endothelial function and prevents diabetes-associated dysmetabolism.

通过 LPCAT1 调节溶血卵磷脂重编程可恢复内皮功能并预防糖尿病相关的代谢紊乱。

Automating Vascular Biology: An End-to-End Automated Workflow for High-Throughput Blood Vessel-on-a-Chip Production and Multi-Site Validation.

血管生物学自动化:用于高通量芯片血管生产和多站点验证的端到端自动化工作流程。

Lin Dawn S Y, Mohammad Hashemi Hanieh, Asadi Jozani Kimia, Chakravarty Anushree, Kouthouridis Sonya, Bonanno Jessica, Anvari Nicky, Rajasekar Shravanthi, Zhang Feng, Cheng Richard Y, Singh Narendra Kumar, Medina Luis Miguel, Durante Marc, He Yufang, Zhang Boyang

Bioengineered Lymphatic Vessels in Synthetic Matrices to Study Breast Cancer Cell Functions.

利用合成基质中的生物工程淋巴管研究乳腺癌细胞功能。

Odabasi Rodi, Krattiger Lisa A, Kanari Magdalini, Jacobs Mira A, Moser Lukas O, Tibbitt Mark W, Halin Cornelia, Ehrbar Martin

Macrophage pyroptosis inhibition alleviates postinjury neointimal formation and vascular restenosis.

抑制巨噬细胞焦亡可减轻损伤后新生内膜形成和血管再狭窄。

Ji Zaixiong, He Meijuan, Wu Hong, Chen Shixiong, Wang Suhe, Yin Xiaorui, Wang Han

RAB5C Increases Endothelial Release of VWF by Regulating Vesicle Trafficking.

RAB5C 通过调节囊泡运输增加内皮细胞释放 VWF。

Reventun Paula, Toledano-Sanz Pablo, Delgado-Marin Maria, Viskadourou Maria, Foster D Brian, de Vries Paul S, Sabater-Lleal Maria, Alcharani Nunzio, Gonzalez-Cucharero Claudia, Osburn William O, Morrison Alanna C, Wolberg Alisa S, Smith Nicholas L, Arvanitis Marios, Lowenstein Charles J
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