WB | 咨询技术 | Human,Mouse,Rat |
IF | 咨询技术 | Human,Mouse,Rat |
IHC | 1/100-1/300 | Human,Mouse,Rat |
ICC | 1/200-1/1000 | Human,Mouse,Rat |
FCM | 咨询技术 | Human,Mouse,Rat |
Elisa | 1/10000 | Human,Mouse,Rat |
Aliases | EEF2; EF2; Elongation factor 2; EF-2 |
Entrez GeneID | 1938; |
WB Predicted band size | 100kDa |
Host/Isotype | Rabbit IgG |
Antibody Type | Primary antibody |
Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
Species Reactivity | Human,Mouse,Rat |
Immunogen | Synthesized peptide derived from human EF-2 around the phosphorylation site of T56. |
Formulation | Purified antibody in PBS with 0.05% sodium azide,0.5%BSA and 50% glycerol. |
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以下是关于EF-2 (Phospho-Thr56)抗体的3篇参考文献示例,包括文献名称、作者及摘要概括:
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1. **文献名称**: *"Regulation of elongation factor-2 phosphorylation by amino acid availability in mammalian cells"*
**作者**: Smith, J. et al.
**摘要**: 研究揭示了氨基酸剥夺通过激活eEF-2激酶导致EF-2 Thr56位点磷酸化的机制,利用Phospho-Thr56抗体通过Western blot验证了这一过程,表明其对蛋白质翻译的抑制作用。
2. **文献名称**: *"AMP-activated protein kinase signaling regulates eEF2 phosphorylation in response to energy stress"*
**作者**: Horman, S. et al.
**摘要**: 探讨AMPK在能量应激下调控eEF-2激酶活性及EF-2 Thr56磷酸化的作用,通过该抗体在骨骼肌细胞中检测磷酸化水平,揭示其与代谢抑制的关联。
3. **文献名称**: *"Phosphorylation of elongation factor-2 by CDK1 modulates protein synthesis during mitosis"*
**作者**: Wang, X. et al.
**摘要**: 发现CDK1在有丝分裂期间直接磷酸化EF-2 Thr56位点,使用特异性抗体证实其磷酸化状态,并证明其对细胞周期依赖性翻译调控的影响。
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这些示例基于领域常见研究方向,实际文献需通过学术数据库核实。如需具体文章,建议检索关键词“EF-2 Phospho-Thr56 antibody”或相关信号通路(如mTOR、AMPK)。
The EF-2 (Phospho-Thr56) antibody is designed to detect elongation factor 2 (EF-2) when phosphorylated at threonine 56. a post-translational modification critical for regulating protein synthesis. EF-2 is a GTP-binding protein essential for the translocation step during mRNA translation, facilitating the movement of tRNA and mRNA within the ribosome. Phosphorylation at Thr56 is catalyzed by EF-2 kinase (eEF2K), which inhibits EF-2’s activity, thereby temporarily halting elongation and reducing global protein synthesis. This regulatory mechanism is often activated under stress conditions, such as nutrient deprivation, hypoxia, or energy depletion, to conserve cellular resources.
The antibody serves as a key tool for studying translational control, cellular stress responses, and signaling pathways involving eEF2K. It is widely used in techniques like Western blotting, immunofluorescence, and immunoprecipitation to assess EF-2 phosphorylation status in various experimental models. Dysregulation of EF-2 phosphorylation has been implicated in diseases such as cancer, neurodegenerative disorders, and cardiovascular conditions, where aberrant protein synthesis or stress adaptation pathways contribute to pathogenesis. Researchers also utilize this antibody to investigate therapeutic interventions targeting translation machinery or eEF2K activity. Specificity for the phosphorylated Thr56 epitope ensures minimal cross-reactivity, making it reliable for distinguishing active/inactive EF-2 states in complex biological samples.
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