肌动蛋白是一类形成微丝的球状多功能蛋白质 。它基本上存在于所有真核细胞中 ,进化过程中高度保守。细胞肌动蛋白以单体和聚合体形式存在于真核细胞内,其中单体小球又称为G-肌动蛋白(Globular Actin,G-actin);多个G-肌动蛋白以双螺旋结构聚合形成纤维化肌动蛋白,称为F-肌动蛋白(Fibros Actin,F-actin),又称为微丝,是细胞骨架最主要的结构组分之一。
G-Actin/F-Actin这2种形式在一定生理条件下相互转换,在微丝正极组装和负极去组装同时存在的现象,此现象被命名为“踏车现象”(TreadMilling),并在细胞内保持平衡状态,参与细胞一系列的生理功能。当G-Actin/F-Actin在细胞内比值发生改变时,意味着细胞结构,运动形态和稳态的变化。
因此G-Actin/F-Actin比值的检测,常被用于:
1.研究药物化合物对细胞稳态的影响。
2.研究突变的细胞系与野生型细胞的变化。
3.研究环境的变化对细胞的应激。
作为专业的生命科学医药原料供应商,CytoSkeleton中国区金牌代理,艾美捷科技为您推荐:G-Actin/F-Actin比值分析试剂盒( G-Actin:F-Actin 细胞体内分析试剂盒 )
名称 | G-Actin/F-Actin比值分析试剂盒 G-Actin : F-Actin In Vivo Assay Kit |
货号 | CSK-BK037 |
品牌 | |
说明书下载 | 点击下载 |
原理 | ? Western blot定量分析F-actin和G-actin比值: 细胞在以洗涤剂为基础的裂解缓冲液中被裂解,该缓冲液能稳定和维持G型和F型细胞肌动蛋白。F-形式的细胞肌动蛋白。该缓冲液可溶解G型肌动蛋白,但不会溶解F型肌动蛋白。离心步骤使F-肌动蛋白颗粒化,将G-肌动蛋白留在上清液中。样品上清液和颗粒在SDS-PAGE系统中运行,通过WB分析对肌动蛋白进行定量。 |
适用样品 | 悬浮细胞,贴壁细胞,组织样本 |
试剂盒组分 | 1. Lysis and F-actin stabilization buffer 2. ATP (Cat. # BSA04) 3. Protease inhibitor cocktail (Cat. # PIC02) 4. F-actin enhancing control solution 5. F-actin depolymerization control solution 6. Control G-actin Standard (Cat. # AKL99) 7. Anti-Actin MAb (clone 7A8.2.1) (Cat # AAN02-S) 8. SDS sample buffer (5 x) 9. DMSO 10. Manual with detailed protocols and extensive troubleshooting guide |
保存条件 | 参考产品说明书,按照要求保存各组分 |
* 本产品仅适用于科研用途.
常见问题FAQ:
G-Actin/F-Actin比值分析试剂盒的实验中,进行到哪一步,可暂停实验?
直到在37°C下以100,000xg旋转1小时后才能停止测定。高速离心后,可以将上清液(G-肌动蛋白)与SDS上样缓冲液混合并冷冻以备后用。沉淀物(F-肌动蛋白)应该用解聚剂和水重新悬浮,然后与SDS上样缓冲液混合并冷冻以备后用。冷冻后,F-肌动蛋白解聚,因此有必要在冷冻样品之前将F-肌动蛋白与G-肌动蛋白分离,以分离样品以准确测量F-肌动蛋白和G-肌动蛋白的比率。
G-Actin/F-Actin比值分析试剂盒的灵敏度多高?
该测定可以检测到G-肌动蛋白与F-肌动蛋白比率的小至15%的变化。每个条件都应一式两份进行并重复多次,因为实验之间的检测重现性可能会有10-20%的差异。
G-Actin/F-Actin比值分析试剂盒能否在较慢的离心速度(如16,000g)下工作?
抱歉不行。在我们的测试离心速度是发现,如果低于100,000xg,哪怕是26,000 g,未能有效地沉淀F-肌动蛋白。
结果展示:
3T3 swiss小鼠胚胎成纤维细胞系: P=不可溶的F-actin;S=可溶性的G-actin Panel 1 : 正常未处理细胞 Panel 2:肌动蛋白聚合药物jasplakinolide处理 G-actin/F-actin ≈ 45/55 | Cul3+/+ 小鼠与Cul3+/? 小鼠的比较: G-actin/F-actin ≈ 45/55 |
CytoSkeleton厂家质检测试 | Nature communications doi.org/10.1038/s41467-021-23123-x |
*以上结果仅供参考,因细胞系的不同,细胞所处的运动状态,药物与环境刺激不同,G-actin/F-actin的比值会有较大的浮动,建议参考相同细胞系的已发表文献。
部分发表文章展示:
Morandell, Jasmin, et al. "Cul3 regulates cytoskeleton protein homeostasis and cell migration during a critical window of brain development." Nature communications1 (2021): 1-22.
Lu, Yi-Ju, et al. "Arabidopsis calcium-dependent protein kinase 3 regulates actin cytoskeleton organization and immunity." Nature communications1 (2020): 1-12.
Bojcevski, Jovana et al. “Influence of retinal NMDA receptor activity during autoimmune optic neuritis.” Journal of neurochemistry vol. 153,6 (2020): 693-709. doi:10.1111/jnc.14980
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Bojcevski J, Stojic A, Hoffmann DB, Williams SK, Müller A, Diem R, Fairless R. Influence of retinal NMDA receptor activity during autoimmune optic neuritis. J Neurochem. 2020 Jun;153(6):693-709. doi: 10.1111/jnc.14980. Epub 2020Mar 3. PMID: 32031240.
Kommaddi, Reddy Peera et al. “Aβ mediates F-actin disassembly in dendritic spines leading to cognitive deficits in Alzheimer's disease.” The Journal of neuroscience : the official journal of the Society for Neuroscience vol. 38,5 (2018): 1085-1099. doi:10.1523/JNEUROSCI.2127-17.2017
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Liu et al., 2012. TLR2 Is a Primary Receptor for Alzheimer's Amyloid β Peptide To Trigger Neuroinflammatory Activation. J. Immunol. 188, 1098-1107.
Chand et al., 2012. C-terminal region of teneurin-1 co-localizes with dystroglycan and modulates cytoskeletal organization through an extracellular signal-regulated kinase-dependent stathmin- and filamin A-mediated mechanism in hippocampal cells. Neuroscience. 219, 255-270.
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Zhang et al., 2005. Activation of the Arp2/3 complex by N-WASP is required for actin polymerization and contraction in smooth muscle. Am. J. Physiol. 288, C1145-C1160.
Chen et al., 2004. Protective effect of phosphatidylinositol 4,5-bisphosphate against cortical filamentous actin loss and insulin resistance induced by sustained exposure of 3T3-L1 adipocytes to insulin. J. Biol. Chem. 279, 39705-39709.
Tang and Gunst, 2004. The small GTPase Cdc42 regulates actin polymerization and tension development during contractile stimulation of smooth muscle. J. Biol. Chem. 279, 51722-51728.
Searles et al., 2004. Actin cytoskeleton organization and poststranscriptional regulation of endothelial nitric oxide synthase during cell growth. Circ. Res. 95, 488-495.
Tu et al., 2003. Migfilin and Mig-2 link focal adhesions to filamin and the actin cytoskeleton and function in cell shape modulation. Cell. 113, 37-47.
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