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Merck

SAB4200649

Sigma-Aldrich

Monoclonal Anti-MASTL antibody produced in mouse

clone 2C8/D11, purified from hybridoma cell culture

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About This Item

UNSPSCコード:
12352203
NACRES:
NA.41

由来生物

mouse

抗体製品の状態

purified immunoglobulin

抗体製品タイプ

primary antibodies

クローン

2C8/D11, monoclonal

フォーム

buffered aqueous solution

分子量

~100 kDa

交差性

human, monkey

濃度

~1 mg/mL

テクニック

flow cytometry: 10-20 μg/test using using human HeLa cells.
immunoblotting: 1-2 μg/mL using whole extracts of human HeLa cells.
immunofluorescence: 10-20 μg/mL using using human HeLa cells.

アイソタイプ

IgG2b

UniProtアクセッション番号

輸送温度

dry ice

保管温度

−20°C

ターゲットの翻訳後修飾

unmodified

遺伝子情報

mouse ... Mastl(67121)

詳細

Monoclonal Anti-MASTL (mouse IgG2b isotype) is derived from the hybridoma 2C8/D11 produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice immunized with a fusion protein. Microtubule-Associated Serine/Threonine kinase-Like (MASTL), also known as GREATWALL (GWL) in Drosophila and Xenopus is localized to the nucleus but, during M-phase it is activated and re-localized to the centrosomes.

免疫原

immunized with a fusion protein of 250aa polypeptide from the region that divides the kinase domain of mouse MASTL

アプリケーション

Monoclonal Anti-MASTL antibody produced in mouse may be used in various immunochemical techniques including immunoblotting, flow cytometry and immunofluorescence.

生物化学的/生理学的作用

Microtubule-associated serine/Threonine kinase-Like (MASTL) acts as a cell cycle marker of M phase. It has an ability to regulate mitosis entry, anaphase and cytokinesis. In Drosophila MASTL (Greatwall) was initially identified as a kinase essential for chromosome condensation. MASTL enhances cyclin B1-Cdk1-dependent mitotic phosphorylation events. Furthermore, MASTL is also an inhibitor of the tumor suppressor protein Phosphatase 2A (PP2A), and thus maintains the equilibrium between cyclin B-Cdk1 and PP2A. A missense mutation in the MASTL gene leads to the development of autosomal dominant inherited thrombocytopenia.

物理的形状

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

免責事項

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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保管分類コード

10 - Combustible liquids

WGK

WGK 1

引火点(°F)

Not applicable

引火点(℃)

Not applicable


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文書ライブラリにアクセスする

Thierry Lorca et al.
Genes & cancer, 3(11-12), 712-720 (2013-05-02)
Mitotic division is induced by protein phosphorylation. For a long time the supported hypothesis was that mitotic entry and exit were the exclusive result of cyclin B-Cdk1 kinase activation and inactivation, whereas the phosphatase activity required to dephosphorylate mitotic substrates
Erik Voets et al.
Cell cycle (Georgetown, Tex.), 9(17), 3591-3601 (2010-09-08)
Greatwall (Gwl) was originally discovered in Drosophila as an essential kinase for correct chromosome condensation and mitotic progression. In Xenopus, Gwl may influence the positive-feedback loop that directs cyclin B1-Cdk1 activation and the mitotic state by inhibiting the phosphatase PP
Loss of human Greatwall results in G2 arrest and multiple mitotic defects due to deregulation of the cyclin B-Cdc2/PP2A balance
Burgess A, et al.
Proceedings of the National Academy of Sciences of the USA, 107(28), 12564-12569 (2010)
Marcos Malumbres
Physiological reviews, 91(3), 973-1007 (2011-07-12)
The basic biology of the cell division cycle and its control by protein kinases was originally studied through genetic and biochemical studies in yeast and other model organisms. The major regulatory mechanisms identified in this pioneer work are conserved in

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