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TAMRA NHS ester, 6-isomer
| 目录号 | 数量 | 价格 | 提前通知时间 | 购买此产品 |
|---|---|---|---|---|
| 18120 | 1 mg | $110 | 现货 | |
| 28120 | 5 mg | $210 | 现货 | |
| 48120 | 25 mg | $350 | 现货 | |
| 58120 | 50 mg |
$595
|
现货 | |
| 68120 | 100 mg |
$790
|
现货 |
TAMRA (tetramethylrhodamine) is a xanthene dye with a fluorescence maximum at 567 nm.
This product is an N-Hydroxysuccinimide (NHS)-ester of TAMRA dye. Pure 6-isomer. TAMRA NHS-ester readily reacts with various amines and is used to generate fluorescently labeled proteins, peptides, antibodies, and other biomolecules.
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AF 430 NHS ester
AF 430 is a hydrophilic coumarin dye with emission in the green-yellow range. The NHS ester is used for the labeling of amine groups.叠氮-peg4-叠氮化物 (Azide-peg4-azide)
PEG4 二叠氮是具有两个叠氮基团的同型双功能连接体。它可通过点击化学用于合成具有亲水核心的二聚体分子。JOE 亚磷酰胺，6-异构体 (JOE phosphoramidite, 6-isomer)
JOE 染料亚磷酰胺用于合成标记寡核苷酸。 JOE 吸收和发射最大值介于 FAM 和 TAMRA/ROX 染料的最大值之间。
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General properties
| Appearance: | red powder |
| Molecular weight: | 527.53 |
| CAS number: | 150810-69-8 |
| Molecular formula: | C29H25N3O7 |
| IUPAC name: | 2-(6-(dimethylamino)-3-(dimethyliminio)-3H-xanthen-9-yl)-4-(((2,5-dioxopyrrolidin-1-yl)oxy)carbonyl)benzoate |
| Solubility: | good in DMF, DMSO |
| Quality control: | NMR 1H, HPLC-MS (90%) |
| Storage conditions: | Storage: 12 months after receipt at -20°C in the dark. Transportation: at room temperature for up to 3 weeks. Avoid prolonged exposure to light. Desiccate. |
| 安全数据表（MSDS）: | 下载 |
| 产品规格 |
Spectral properties
| Excitation/absorption maximum, nm: | 541 |
| ε, L⋅mol−1⋅cm−1: | 84000 |
| Emission maximum, nm: | 567 |
| Fluorescence quantum yield: | 0.1 |
| CF260: | 0.34 |
| CF280: | 0.17 |
产品引用
- Wiesner, W.; Kühnel, R. M.; Pomorski, T. G. Synthesis and Purification of Lipid-Conjugated Fluorescent PH Sensors. Bio Protoc, 2023, 13(11), e4694. doi: 10.21769/BioProtoc.4694
- Dong, B.; Du, S.; Wang, C.; Fu, H.; Li, Q.; Xiao, N.; Yang, J.; Xue, X.; Cai, W.; Liu, D. Reversible Self-Assembly of Nanoprobes in Live Cells for Dynamic Intracellular pH Imaging. ACS Nano, 2019, 13(2), 1421–1432. doi: 10.1021/acsnano.8b07054
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