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Beta-Catenin (CTNNB1) (3F13) Mouse Monoclonal antibody

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产品基本信息

产品货号
BD-PE1286
产品名称
Beta-Catenin (CTNNB1) (3F13) Mouse Monoclonal antibody
类别
常规抗体
基因名称
CTNNB1
推荐应用
WB
反应种属
Human,Dog,Rat,Monkey,Mouse
存储缓冲液
PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% New type preservative N.
免疫原
Full length human recombinant protein of human CTNNB1 (NP_001895) produced in HEK293T cell.
特异性
Validated through 10k CHIP testing,using a High-Density Protein Microarray that was spotted with ~17,000 various over-expressed proteins to test for antibody specificity.
稀释度
WB 1:500~2000, IHC 1:150, FCM 1:100
预测分子量
85.3kDa
运输及保存条件
-20°C/1 year
宿主
Mouse
同种型
IgG1
背景介绍
The protein encoded by this gene is part of a complex of proteins that constitute adherens junctions (AJs). AJs are necessary for the creation and maintenance of epithelial cell layers by regulating cell growth and adhesion between cells. The encoded protein also anchors the actin cytoskeleton and may be responsible for transmitting the contact inhibition signal that causes cells to stop dividing once the epithelial sheet is complete. Finally, this protein binds to the product of the APC gene, which is mutated in adenomatous polyposis of the colon. Mutations in this gene are a cause of colorectal cancer (CRC), pilomatrixoma (PTR), medulloblastoma (MDB), and ovarian cancer. Three transcript variants encoding the same protein have been found for this gene.
期货
现货
纯化
Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)

OriGene overexpression protein microarray chip was immunostained with UltraMAB anti-beta-catenin mouse monoclonal antibody . The positive reactive proteins are highlighted with two red arrows in the enlarged subarray. All the positive controls spotted in this subarray are also labeled for clarification. These data show that UltraMAB anti-beta-catenin very specifically recognizes beta-catenin antigen on OriGene protein microarray chip.

Flow cytometric Analysis of Hela cells, using anti-CTNNB1 antibody (BD-PE1286), (Red), compared to a nonspecific negative control antibody, (Blue).

MDCK cells were treated either with 30mM NaCl as negative control (left) or with GSK-3beta kinase inhibor 30mM LiCl (right) for 48 hrs. Anti-beta-catenin monoclonal antibody was used for immunofluorescent staining.

Immunohistochemical staining of paraffin-embedded mouse kidney tissue using anti-CTNNB1 4 mouse monoclonal antibody. HIER TEE buffer pH9 at 110C for 10 min, BD-PE1286 (1:100). Detection was done with Klear Mouse (C/N ) DAB Kit.

Immunohistochemical staining of paraffin-embedded mouse lung tissue using anti-CTNNB1 4 mouse monoclonal antibody. HIER TEE buffer pH9 at 110C for 10 min, BD-PE1286 (1:100). Detection was done with Klear Mouse (C/N ) DAB Kit.

Western blot analysis of extracts (35ug) from 9 different cell lines by using anti-CTNNB1 monoclonal antibody .

Immunohistochemical staining of paraffin-embedded mouse small intestine tissue using anti-CTNNB1 4 mouse monoclonal antibody. HIER TEE buffer pH9 at 110C for 10 min, BD-PE1286 (1:100). Detection was done with Klear Mouse (C/N ) DAB Kit.

HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY CTNNB1 (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-CTNNB1 (1:500).

Immunohistochemical staining of paraffin-embedded mouse brain tissue using anti-CTNNB1 4 mouse monoclonal antibody. HIER TEE buffer pH9 at 110C for 10 min, BD-PE1286 (1:100). Detection was done with Klear Mouse (C/N ) DAB Kit.

Immunohistochemical staining of paraffin-embedded mouse spleen tissue using anti-CTNNB1 4 mouse monoclonal antibody. HIER ACCEL buffer (pH8.7) at 110C for 10 min, BD-PE1286 (1:100). Detection was done with Klear Mouse (C/N ) DAB Kit.

Western Blot analysis of 10 different human tissue lysates (10ug) by using Anti-β-Catenin monoclonal antibody

Immunohistochemical staining of paraffin-embedded Mouse colon tissue using anti-beta-catenin mouse monoclonal antibody.

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