WB | 1/500-1/1000 | Human,Mouse,Rat,Hamster |
IF | 1/20 | Human,Mouse,Rat,Hamster |
IHC | 1/50-1/100 | Human,Mouse,Rat,Hamster |
ICC | 技术咨询 | Human,Mouse,Rat,Hamster |
FCM | 咨询技术 | Human,Mouse,Rat,Hamster |
Elisa | 咨询技术 | Human,Mouse,Rat,Hamster |
Aliases | 60S acidic ribosomal protein P1; AA409079; AI325195; AU020965; HSSB; ik:tdsubc_2g1; M(2)21C; MGC137236; OTTHUMP00000004008; p32; p34; RCJMB04_6d17 replication protein A2; 32kDa; REPA 2; REPA1; REPA2; Replication factor A protein 2; Replication protein A 32 kDa subunit; Replication protein A 32kDa subunit; Replication protein A 34 kDa subunit; Replication protein A; replication protein A1 (70kD); Replication Protein A2 (32kDa); Replication protein A2 32kD; Replication protein A2 32kDa; Replication protein A2; Replication protein A2; 32kDa; RF A; RF-A protein 2; Rf-A2; RFA; RFA2_HUMAN; RP A; RP-A p32; RP-A p34; RP21C; RPA 2; RPA 32; RPA; RPA2; RPA32; RPA34; RPA70; RpLP1; RpP2; xx:tdsubc_2g1; zgc:109822. |
Entrez GeneID | 6118 |
WB Predicted band size | Calculated MW: 29 kDa; Observed MW: 29 kDa |
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,Hamster |
Immunogen | A synthetic peptide of human RPA32/RPA2 |
Formulation | Purified antibody in TBS with 0.05% sodium azide,0.05%BSA and 50% glycerol. |
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以下是关于RPA32抗体的3篇参考文献及其摘要内容概览:
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1. **文献名称**: *RPA subunit phosphorylation facilitates chromatin remodeling and homologous recombination at sites of DNA damage*
**作者**: Binz, S.K., Sheehan, A.M., Wold, M.S.
**摘要**: 研究利用RPA32抗体验证其在DNA损伤位点的招募,发现RPA32的磷酸化修饰通过促进染色质重塑复合体(如Rad51)的募集,增强同源重组修复效率。实验表明RPA32抗体在免疫荧光中特异性标记DNA损伤灶。
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2. **文献名称**: *Coordination of DNA damage responses via the Smc5/Smc6 complex*
**作者**: Sleeth, K.M., Sorensen, C.S., Syljuåsen, R.G. et al.
**摘要**: 通过RPA32抗体进行免疫沉淀和Western blot分析,证明Smc5/Smc6复合物与RPA32在DNA复制应激中的相互作用,调控复制叉稳定性及修复通路选择(如HR或NHEJ)。
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3. **文献名称**: *Phosphorylated RPA32 is a critical marker for activation of the ATR-dependent DNA damage response*
**作者**: Anantha, R.W., Sokolova, E., Borowiec, J.A.
**摘要**: 研究使用RPA32磷酸化特异性抗体,证实RPA32的Ser33位点磷酸化是ATR激酶活化的关键标志,揭示了其在DNA损伤信号转导中的早期调控作用。
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**备注**:以上文献均以RPA32抗体作为核心实验工具,涉及DNA损伤应答、修复机制及蛋白质相互作用研究。如需具体期刊信息或DOI,可进一步补充。
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