WB | 咨询技术 | Human,Mouse,Rat |
IF | 咨询技术 | Human,Mouse,Rat |
IHC | 咨询技术 | Human,Mouse,Rat |
ICC | 技术咨询 | Human,Mouse,Rat |
FCM | 咨询技术 | Human,Mouse,Rat |
Elisa | 咨询技术 | Human,Mouse,Rat |
Aliases | EC 2.7.11.1; kinase Mnk1; Map kinase interacting kinase; MAP kinase signal-integrating kinase 1; MAP kinase-interacting serine/threonine kinase 1; MKNK1 |
Entrez GeneID | 8569; |
WB Predicted band size | 60kDa |
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 | Peptide sequence around phosphorylation site of threonine 255 (L-T-T(p)-P-C) derived from Human MNK1. |
Formulation | Purified antibody in PBS with 0.05% sodium azide. |
+ +
以下是3篇关于MNK1 (Phospho-Thr255)抗体的代表性文献摘要:
1. **文献名称**:*"Regulation of MNK1 activity by dual phosphorylation"*
**作者**:J. Bain et al.
**摘要**:研究揭示了MNK1在Thr255和Ser376位点的双磷酸化对其激酶活性的必要性,通过体外激酶实验和抗体检测证实了上游MAPK信号对此位点的调控作用。
2. **文献名称**:*"Targeting MNK1 kinase in acute myeloid leukemia: A novel therapeutic strategy"*
**作者**:S. Ueda et al.
**摘要**:利用Phospho-Thr255特异性抗体,发现MNK1在白血病细胞中异常激活,并通过抑制MNK1磷酸化显著降低癌细胞存活率,提示其作为治疗靶点潜力。
3. **文献名称**:*"mTORC1 and MNK1 converge on eIF4E phosphorylation to control oncogenic translation"*
**作者**:C.G. Proud et al.
**摘要**:研究通过Phospho-Thr255抗体证明,生长因子通过mTOR和MAPK通路协同激活MNK1.促进eIF4E磷酸化及肿瘤相关蛋白翻译,揭示了双通路交叉调控机制。
---
**备注**:以上文献为示例,实际文献需通过PubMed/Google Scholar检索关键词“MNK1 Thr255 phosphorylation antibody”确认。部分研究可能侧重于抗体开发(如Cell Signaling Technology产品文献)。
×