Fluorofurimazine
目录号 : GC68291Fluorofurimazine 是Antares 的荧光底物 (fluorogenic substrate)。Fluorofurimazine 可以实现灵敏的生物发光成像,延长高灵敏度光的产生。Fluorofurimazine具有良好的水溶性,可向小鼠提供更高剂量。Fluorofurimazine 可用于生物发光成像。
Cas No.:2412089-96-2
Sample solution is provided at 25 µL, 10mM.
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- Purity: >98.00%
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Fluorofurimazine is fluorogenic substrate for Antares. Fluorofurimazine can realize sensitive bioluminescence imaging to prolong the generation of high-sensitivity light. Fluorofurimazine has good aqueous solubility allows delivery of higher doses to mice. Fluorofurimazine can be used in the bioluminescence imaging[1].
Fluorofurimazine (562 μg; i.p.; for 30 days; nude mice) increases in peak signal when administered at 562 μg in vivo[1].
Animal Model: | Nude mice[1] |
Dosage: | 562 μg |
Administration: | Intraperitoneal injection;for 30 days |
Result: | Exhibited threefold bioluminescence than AkaLuc with AkaLumine. |
[1]. Su Y, et, al. Novel NanoLuc substrates enable bright two-population bioluminescence imaging in animals. Nat Methods. 2020 Aug;17(8):852-860.
Cas No. | 2412089-96-2 | SDF | Download SDF |
分子式 | C24H18F2N4O2 | 分子量 | 432.42 |
溶解度 | 储存条件 | Store at -20°C | |
General tips | 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。 为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。 |
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Shipping Condition | 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。 |
制备储备液 | |||
1 mg | 5 mg | 10 mg | |
1 mM | 2.3126 mL | 11.5628 mL | 23.1257 mL |
5 mM | 0.4625 mL | 2.3126 mL | 4.6251 mL |
10 mM | 0.2313 mL | 1.1563 mL | 2.3126 mL |
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方) | ||||||||||
% DMSO % % Tween 80 % saline | ||||||||||
计算重置 |
计算结果:
工作液浓度: mg/ml;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,
体内配方配制方法:取 μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL saline,混匀澄清。
1. 首先保证母液是澄清的;
2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。
Novel NanoLuc substrates enable bright two-population bioluminescence imaging in animals
Nat Methods 2020 Aug;17(8):852-860.PMID:32661427DOI:10.1038/s41592-020-0889-6.
Sensitive detection of two biological events in vivo has long been a goal in bioluminescence imaging. Antares, a fusion of the luciferase NanoLuc to the orange fluorescent protein CyOFP, has emerged as a bright bioluminescent reporter with orthogonal substrate specificity to firefly luciferase (FLuc) and its derivatives such as AkaLuc. However, the brightness of Antares in mice is limited by the poor solubility and bioavailability of the NanoLuc substrate furimazine. Here, we report a new substrate, hydrofurimazine, whose enhanced aqueous solubility allows delivery of higher doses to mice. In the liver, Antares with hydrofurimazine exhibited similar brightness to AkaLuc with its substrate AkaLumine. Further chemical exploration generated a second substrate, Fluorofurimazine, with even higher brightness in vivo. We used Antares with Fluorofurimazine to track tumor size and AkaLuc with AkaLumine to visualize CAR-T cells within the same mice, demonstrating the ability to perform two-population imaging with these two luciferase systems.
Evaluation of NanoLuc substrates for bioluminescence imaging of transferred cells in mice
J Photochem Photobiol B 2021 Mar;216:112128.PMID:33529963DOI:10.1016/j.jphotobiol.2021.112128.
NanoLuc luciferase recently gained popularity due to its small size and superior bioluminescence performance. For in vivo imaging applications, NanoLuc has been limited by its substrate furimazine, which has low solubility and bioavailability. Herein, we compared the performances of recently reported NanoLuc luciferase substrates for in vivo imaging in mice. Two substrates with improved aqueous solubility, hydrofurimazine and Fluorofurimazine, were evaluated along with three stabilized O-acetylated furimazine analogues, the hikarazines. All 5 analogues, when tested in vitro, displayed greater signal intensity and reaction duration, in comparison to the standard NanoLuc substrate, furimazine. The two best-performing analogues from the in vitro study were selected for further in vivo testing. The NanoLuc/Fluorofurimazine pair demonstrated the highest bioluminescence intensity, post intravenous administration. It was found to be around 9-fold brighter compared to the NanoLuc/furimazine and 11-fold more intense than the NanoLuc/hikarazine-003 pair, with an average of 3-fold higher light emission when the substrate was injected intraperitoneally, in a subcutaneous model. Excitingly, despite the fact that NanoLuc/Fluorofurimazine emits mostly blue light, we prove that cells trapped in mice lungs vasculature could be visualised via the NanoLuc/Fluorofurimazine pair and compare the results to the AkaLuc/AkaLumine system. Therefore, among the tested analogues, Fluorofurimazine enables higher substrate loading and improved optical imaging sensitivity in small animals, upgrading the use of NanoLuc derived bioluminescent systems for deep tissue imaging.