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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
Store at -20℃,2 years.(Avoid freeze/thaw cycles)
- 保质期:
Store at -20℃,2 years.(Avoid freeze/thaw cycles)
- 英文名:
Mad1 (6-21)
- 库存:
现询
- 供应商:
北京索莱宝科技有限公司
- 规格:
10mg/5mg/1mg
| 规格: | 10mg | 产品价格: | ¥2170.0 |
|---|---|---|---|
| 规格: | 5mg | 产品价格: | ¥1550.0 |
| 规格: | 1mg | 产品价格: | ¥620.0 |
| 基本信息 | |
| 产品类型 | 多肽 |
| CAS | No.286373-49-7 |
| 单字母序列 | HPLGSPGSASDLETSGLQEQR |
| 三字母序列 | His-Pro-Leu-Gly-Ser-Pro-Gly-Ser-Ala-Ser-Asp-Leu-Glu-Thr-Ser-Gly-Leu-Gln-Glu-Gln-Arg |
| 分子式 | C89H144N28O35 |
| 分子量 | 2166.29 |
| 纯度 | ≥95% |
| 外观(性状) | 冻干粉;Lyophilized powder |
| 盐体系 | TFA盐;Trifluoroacetate salt |
| 来源 | 合成;Synthetic |
| 储存条件 | Store at -20℃,2 years.(Avoid freeze/thaw cycles) |
| 类别/标签 | 激素和相关肽(Hormone and Related Peptides) |
| 规格 | BNP (1-21), Pro (Human) 是一种含有 21 个氨基酸的多肽;B 型利钠肽 (BNP),一种心脏利钠激素;BNP 与高度同源的心房利钠肽共同形成心脏的双利钠肽系统;BNP 负责心脏器官发生的变化,并与向子宫外生命的过渡有关。 BNP (1-21), Pro (Human) is a peptide containg 21 amino acids. B-Type Natriuretic Peptide (BNP), a cardiac natriuretic hormone. BNP together with the highly homologous atrial natriuretic peptide, it forms a dual natriuretic peptide system of the heart. BNP is responsible for changes in the heart organogenesis and is associated with transition to extrauterine life. |
| In Vitro | 未检测 |
| 单位 | 瓶 |
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文献和实验Using Phospho‐Motif Antibodies to Determine Kinase Substrates
., Graves, D.J., DeMaggio, A.J., Hoekstra, M.F., Blenis, J., Hunter, T., and Cantley, L.C. 1996. A structural basis for substrate specificities of protein Ser/Thr kinases: Primary sequence preference of. casein kinases I and II, NIMA, phosphorylase kinase
Specificity Profiling of Protein‐Binding Domains Using One‐Bead‐One‐Compound Peptide Libraries
without the need for any special equipment, and therefore can be employed in any chemical or biochemical laboratory. OBOC peptide libraries have been widely used to map the ligand specificity of proteins, to determine the substrate specificity of enzymes, and to develop inhibitors
.html): 可一站式支持您从靶点验证、苗头化合物发现到抑制剂活性与选择性优化的全流程研究,助力加速激酶靶向药物的研发与转化。 三、激酶大环虚拟化合物库(www.medchemexpress.cn/screening/kinase-macrocyclic-compound-virtual-library.html),可供虚拟筛选以及定制合成。由于大环的半刚性结构可限制构象与提升亲和力以及优化药代动力学性质,大环化策略是激酶抑制剂优化的理想手段。 产品
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