Powder: -20°C for 3 years | In solvent: -80°C for 1 year
SMCC (N-Succinimidyl 4-(N-maleimidomethyl)cycl) 是一种异双功能蛋白质交联剂。它接合抗原耦合脾脏细胞来诱导抗原特异性免疫反应。
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
50 mg | ¥ 148 | 现货 | ||
100 mg | ¥ 282 | 现货 | ||
1 mL * 10 mM (in DMSO) | ¥ 195 | 现货 |
产品描述 | SMCC (N-Succinimidyl 4-(N-maleimidomethyl)cycl) is a heterobifunctional protein crosslinker. |
体外活性 | N-Succinimidyl 4-(N-maleimidomethyl)cycl(SMCC) is an amine-to-sulfhydryl crosslinker that contains NHS-ester and maleimide reactive groups at opposite ends of a medium-length cyclohexane-stabilized spacer arm (8.3 angstroms). SMCC conjugation occurs via a maleimide group that is sulfhydryl (thiol; -SH) reactive and a NHS ester group that is amine reactive and forms stable, covalent protein crosslinks. |
细胞实验 | Branched PEI (25 kDa) was dissolved in PBS buffer to yield a concentration of 1 mg/mL. No-weigh Sulfo-SMCC was dissolved in Milli-Q water with a concentration of 10 mg/mL, then a certain of the prepared no-weigh SulfoSMCC solution was added into 2 mL PEI solution to incubate for 30 min at 37 C. After the PEI-SMCC polymer was formed, TAT solution was added into the polymer at the given molar ratio and incubated for 2 h at 4 C. The concentration of unreacted SMCC and unreacted TAT were removed using Zeba Spin Desalting Columns. The polymer PEI-SMCC-TAT was also characterized and analyzed through FTIR to check if each element was added to the PEI backbone. |
别名 | N-Succinimidyl 4-(N-maleimidomethyl)cycl, 4-(N-马来酰亚胺基甲基)环己烷-1-羧酸琥珀酰亚胺酯 |
分子量 | 334.32 |
分子式 | C16H18N2O6 |
CAS No. | 64987-85-5 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 25 mg/mL (74.78 mM)
可选溶剂 | 浓度 体积 质量 | 1 mg | 5 mg | 10 mg | 25 mg |
DMSO | 1 mM | 2.9911 mL | 14.9557 mL | 29.9115 mL | 74.7787 mL |
5 mM | 0.5982 mL | 2.9911 mL | 5.9823 mL | 14.9557 mL | |
10 mM | 0.2991 mL | 1.4956 mL | 2.9911 mL | 7.4779 mL | |
20 mM | 0.1496 mL | 0.7478 mL | 1.4956 mL | 3.7389 mL | |
50 mM | 0.0598 mL | 0.2991 mL | 0.5982 mL | 1.4956 mL |
对于不同动物的给药剂量换算,您也可以参考 更多...
请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法: 比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL,一共给药动物10 只,您使用的配方为5% DMSO+30% PEG300+5% Tween 80+60% ddH2O。那么您的工作液浓度为2 mg/mL。
母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。
您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。
SMCC 64987-85-5 Others N-Succinimidyl 4-(N-maleimidomethyl)cycl ADC Linkers inhibit Antibody-drug conjugates linkers Inhibitor 4-(N-马来酰亚胺基甲基)环己烷-1-羧酸琥珀酰亚胺酯 inhibitor