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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
储存条件:-20℃,干燥、避光、密封
- 保质期:
2年
- 英文名:
nmda receptor antagonist/4-(Phosphonomethyl)-2-piperazinecarboxylic acid
- 库存:
1000
- 供应商:
四川省维克奇生物科技有限公司
- CAS号:
113919-36-1
- 规格:
10mg
英文名称:nmda receptor antagonist/4-(Phosphonomethyl)-2-piperazinecarboxylic acid
分子式:C6H13N2O5P
分子量:224.15
CAS:113919-36-1
熔点:No Data Available
沸点:524.8±60.0 °C | Condition: Press: 760 Torr
酸度系数pKa:0.86±0.10 | Condition: Most Acidic Temp: 25 °C
储存条件:-20℃,干燥、避光、密封
规格:5mg10mg20mg50mg100mg500mg1g80g等应客户需求包装
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文献和实验Redox Sensitivity of NMDA Receptors
The redox modulatory sites of the NMDA receptor consist of critical cysteine residues, which when chemically reduced, increase the magnitude of NMDA-evoked responses. In contrast, after oxidation, NMDA-evoked responses are decreased in size
Transient Expression of Functional NMDA Receptors in Mammalian Cells
The NMDA subtype of excitatory glutamate receptor is a multisubunit, fast-acting, ligand-gated cation channel with a high permeability for Ca2+ . NMDA receptors have been shown to be of importance in physiological processes, such as long
Ca2+/Calmodulin-Dependent Protein Kinase II (CaMKII)
to the NMDA-receptor subunit GluN2B (formerly known as NR2B). Here we discuss studying CaMKII by inhibition (including by the novel class of CN inhibitors) and by mutagenesis. We describe purification of CaMKII, activity assays, directing and probing auto
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