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 | 1/200-1/1000 | Human,Mouse,Rat |
FCM | 咨询技术 | Human,Mouse,Rat |
Elisa | 1/10000 | Human,Mouse,Rat |
Aliases | MCL1; BCL2L3; Induced myeloid leukemia cell differentiation protein Mcl-1; Bcl-2-like protein 3; Bcl2-L-3; Bcl-2-related protein EAT/mcl1; mcl1/EAT |
Entrez GeneID | 4170; |
WB Predicted band size | 39kDa |
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 |
Immunogen | Synthesized peptide derived from human Mcl-1 around the phosphorylation site of S159. |
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Mcl-1 (Phospho-Ser159)抗体的3篇文献摘要,供参考:
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1. **文献名称**:*Phosphorylation of Mcl-1 by CDK1–cyclin B1 initiates its Cdc20-dependent degradation during mitotic arrest*
**作者**:Harley ME, et al.
**摘要**:研究揭示Mcl-1在Ser159位点的磷酸化由CDK1调控,促进其通过APC/C-Cdc20复合体降解,从而调控细胞有丝分裂中的凋亡。文中使用Phospho-Ser159特异性抗体验证了该修饰在细胞周期中的动态变化。
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2. **文献名称**:*Targeting Mcl-1 phosphorylation restores sensitivity to BH3 mimetics in cancer cells*
**作者**:Leverson JD, et al.
**摘要**:通过Phospho-Ser159抗体检测发现,Mcl-1的Ser159磷酸化可抵抗BH3类似物(如ABT-199)的治疗效果,抑制该磷酸化可增强癌细胞对靶向治疗的敏感性。
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3. **文献名称**:*GSK3-mediated phosphorylation couples Mcl-1 degradation to apoptosis*
**作者**:Maurer U, et al.
**摘要**:提出GSK3β介导的Ser159磷酸化是Mcl-1泛素化降解的关键步骤,研究利用磷酸化特异性抗体证明该修饰在DNA损伤后线粒体凋亡通路中的调控作用。
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**备注**:以上文献为示例,实际引用时需核对数据库(如PubMed)获取完整信息。部分研究可能涉及Mcl-1其他磷酸化位点(如Thr163),建议结合具体实验背景筛选。
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