Anti-beta Catenin antibody (Ab16051)

CTNNB, OK/SW-cl.35, PRO2286, CTNNB1, Catenin beta-1, Beta-catenin

反应种属:Human
抗原名称:CTNNB1
应用:WB, IHC, ELISA, 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

背景信息

What is this antibody validated in? Anti-beta Catenin antibody (ab16051) is a rabbit polyclonal antibody and is validated for use in Western Blot (WB), Immunohistochemistry (IHC-P), Immunocytochemistry/immunofluorescence (ICC/IF), ELISA in Human samples. What is the molecular weight of beta Catenin? Anti-beta Catenin (ab16051) specifically detects a band for beta Catenin (UniProt: P35222) at a molecular weight of 94kDa. Trusted by the scientific community Anti-beta Catenin (ab16051) was first used in a scientific publication in 2005 and has been cited over 330 times in peer-reviewed journals. Reviewed by scientists Anti-beta Catenin (ab16051) has over 30 independent reviews from customers. Specificity confirmed The specificity of Anti-beta Catenin antibody (ab16051) has been confirmed by Western blot testing in CTNNB1 Knockout HAP1 cells.

文献引用 (315)

MiR-378 mediates the ovariectomy induced bone loss via exaggerating osteoclastogenesis and transforming growth factor beta impaired osteogenesis.

miR-378 通过加剧破骨细胞生成和转化生长因子β损害成骨作用来介导卵巢切除术引起的骨丢失。

Feng Lu, Yang Zhengmeng, Hou Nan, Wang Haixing, Bai Shanshan, Lu Xuan, Wang Yaofeng, Lin Sien, Tortorella Micky D, Li Gang

Inhibiting L-type calcium channel promotes cardiomyocyte proliferation through activating the canonical Wnt signaling pathway.

抑制 L 型钙通道可通过激活经典的 Wnt 信号通路促进心肌细胞增殖。

Feng Meng-Ying, Tang Yan-Song, Yao Su, Zhang Hong-Jie, Liu Bi-Lin, Huang Rong-Rong, Huang Shi-Qi, Ou-Yang Zhao-Hui, Yuan Min, Jiang Rui, Xu Da-Chun, Gong Guo-Hua, Wei Ke

HBx hijacks the miR-19a-3p/BAMBI/TGF-β1 axis to impair the anti-tumour activity of CD4(+) T cells in diffuse large B-cell lymphoma.

HBx 劫持 miR-19a-3p/BAMBI/TGF-β1 轴,从而削弱弥漫性大 B 细胞淋巴瘤中 CD4(+) T 细胞的抗肿瘤活性。

Acute myeloid leukemia (AML)-derived bone mesenchymal stem cell exosomal METTL14 promotes AML cell growth and glycolysis by HOXA3/WNT7B axis.

急性髓系白血病 (AML) 来源的骨髓间充质干细胞外泌体 METTL14 通过 HOXA3/WNT7B 轴促进 AML 细胞生长和糖酵解。

Liu Wanying, Ming Xi, Wu Jiaying, Yan Sijia, Su Shuai, Zheng Rubing, Wang Yu, Xiao Yi

Andrographolide targets syndecan4 to impair its interaction with syntenin and inhibits the biogenesis of small extracellular vesicles.

穿心莲内酯靶向 syndecan4,削弱其与 syntenin 的相互作用,并抑制小细胞外囊泡的生物发生。

Wnt-directed CXCL12-expressing apical papilla progenitor cells drive tooth root formation

Wnt信号通路调控的表达CXCL12的牙根尖乳头祖细胞驱动牙根形成

Mizuki Nagata ,Gaurav T Gadhvi ,Taishi Komori ,Yuki Arai ,Hiroaki Manabe ,Angel Ka Yan Chu ,Ramandeep Kaur ,Meer Ali ,Yuntao Yang ,Chiaki Tsutsumi-Arai ,Yuta Nakai ,Yuki Matsushita ,Nicha Tokavanich ,W Jim Zheng ,Joshua D Welch ,Noriaki Ono ,Wanida Ono

PB2 and NP of North American H5N1 virus drive immune cell replication and systemic infections.

北美H5N1病毒的PB2和NP蛋白驱动免疫细胞复制和全身感染。

Kim Young-Il, Jang Seung-Gyu, Kwon Woohyun, Kim Jaemoo, Park Dongbin, Choi Isaac, Choi Jeong Ho, Gil Juryeon, Yu Mina, Jeong Boyeong, Kim Eun-Ha, Kim Se-Mi, Kim Hyunjoon, Ahn Jae-Woo, Hwang Suhee, Heo Seo-Young, Casel Mark Anthony B, Rollon Rare, Fabrizio Thomas, Webby Richard J, Choi Young Ki

Chronic sublethal exposure to methylmercury lengthens telomeres in developing zebra finches.

长期亚致死剂量接触甲基汞会延长发育中的斑胸草雀的端粒。

Davis Rachel L, Mason Samuel D, Wake Christian, Fabozzi Giulia, Catalano William L, Schramm Chaim A, Henry Amy R, Parker Cokie L, Laboune Farida, McLaughlin Casey L, Kittilson Jeffrey D, Swaddle John P, Cristol Daniel A, Heidinger Britt J, Douek Daniel C

Evaluation of Tideglusib as a Disease Modifying Therapy in Murine Models of Arrhythmogenic Cardiomyopathy.

在致心律失常性心肌病小鼠模型中评估 Tideglusib 作为疾病修饰疗法的疗效

Malhotra Nipun, Cavus Omer, Wallace Michael J, Bobik John T, You Kevin, Takenaka Sarah S, Abdallah Danielle, Mohler Eleanor J, Antwi-Boasiako Steve, Murphy Nathaniel P, Sucharski-Argall Holly, Xu Xianyao, Chelko Stephen P, Hund Thomas J, Roberts Jason D, Mohler Peter J, El Refaey Mona

Activated mTOR Signaling in the RPE Drives EMT, Autophagy, and Metabolic Disruption, Resulting in AMD-Like Pathology in Mice.

RPE 中 mTOR 信号激活驱动 EMT、自噬和代谢紊乱,导致小鼠出现类似 AMD 的病理

Chowdhury Olivia, Bammidi Sridhar, Gautam Pooja, Babu Vishnu Suresh, Liu Haitao, Shang Peng, Xin Ying, Mahally Emma, Nemani Mihir, Koontz Victoria, Lathrop Kira, Kedziora Katarzyna M, Franks Jonathan, Sun Ming, Smith Joshua W, DeVine Lauren R, Cole Robert N, Stepicheva Nadezda, Strizhakova Anastasia, Chattopadhyay Sreya, Hose Stacey, Zigler Jacob Samuel Jr, Sahel José-Alain, Qian Jiang, Guha Prasun, Handa James T, Ghosh Sayan, Sinha Debasish
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