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 | CHEK1; CHK1; CHK1 checkpoint homolog; |
Entrez GeneID | 1111; |
WB Predicted band size | 55kDa |
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 |
Immunogen | Peptide sequence around phosphorylation site of serine 286 (S-E-S(p)-P-S) derived from Human Chk1. |
Formulation | Purified antibody in PBS with 0.05% sodium azide. |
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以下是3篇涉及Chk1 (Phospho-Ser286)抗体的参考文献摘要:
1. **"Phosphorylation of Chk1 by ATR is antagonized by a Chk1-regulated phosphatase"**
- *Authors: Zhao H, Piwnica-Worms H*
- 摘要:研究揭示了DNA损伤后ATR对Chk1 Ser286位点的磷酸化激活机制,并发现Chk1可通过调控磷酸酶活性反向调节自身磷酸化状态,维持检查点信号动态平衡。
2. **"Human cell cycle checkpoint kinase hChk1 is phosphorylated at serine 286 by ATR in response to replication stress"**
- *Authors: Smits VA, Reaper PM, Jackson SP*
- 摘要:证实复制压力下ATR直接磷酸化Chk1的Ser286位点,该修饰对Chk1激活及下游检查点调控至关重要,并利用特异性抗体验证了磷酸化信号与细胞周期停滞的关联。
3. **"ATM- and cell cycle-dependent regulation of ATR in response to DNA double-strand breaks"**
- *Authors: Gatei M, et al.*
- 摘要:探讨DNA双链断裂后ATM与ATR协同调控Chk1磷酸化(包括Ser286位点)的机制,通过Phospho-Ser286抗体检测发现该修饰依赖ATM/ATR信号通路的交叉对话。
4. **"Conservation of the Chk1 checkpoint pathway in mammals: linkage of DNA damage to Cdk regulation through Cdc25"**
- *Authors: Chen MS, et al.*
- 摘要:早期研究鉴定了Chk1多个磷酸化位点(含Ser286),证明其磷酸化与Cdc25调控及细胞周期停滞相关,为后续抗体开发提供了理论基础。
注:以上文献年份集中在1999-2006年,侧重经典机制研究。如需近年技术应用文献,可补充说明。
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