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引用和文献 (25)
Invitrogen™
6-ROX（6-羧基-X-罗丹明），单异构体
6-ROX（6-羧基-X-罗丹明），单异构体
| 货号 | 数量 |
|---|---|
| C6156 又称 C-6156 | 10 mg |
货号 C6156
又称 C-6156
价格（CNY)
4,502.00
Each
数量:
10 mg
价格（CNY)
4,502.00
Each
The excitation and emission spectra of carboxyrhodamine 6G (CR 6G) fall between those of fluorescein and tetramethylrhodamine. With a peak absorption at 525 nm, conjugates of carboxyrhodamine 6G are an excellent match to the 514 nm spectral line of the argon-ion laser. The amine-reactive 6-CR 6G, SE can be used to attach this fluorophore to biomolecules of interest including amine-modified oligonucleotides.
羧基罗丹明 6G (CR 6G) 的激发和发射光谱介于荧光素和四甲基罗丹明之间。在 525 nm 处出现峰吸收，羧基罗丹明 6G 的偶联物与氩离子激光的 514 nm 光谱非常匹配。胺反应性 6-CR 6G, SE 可用于将该荧光基团连接至目标生物分子，包括经胺修饰的寡核苷酸。
仅供科研使用。不可用于诊断程序。
规格
化学反应性胺
发射525
激发514
标签或染料ROX
产品类型6-ROX
数量10 mg
反应一部分羧酸
运输条件室温
标签类型经典染料
Unit SizeEach
内容与储存
储存在冰箱(-5 至 -30°C)中并避光。
常见问题解答 (FAQ)
What is the excitation and emission wavelength for rhodamine?
引用和文献 (25)
引用和文献
Abstract
Cross-resistance to antifolates in multidrug resistant cell lines with P-glycoprotein or multidrug resistance protein expression.
Journal:Biochem Pharmacol
PubMed ID:9256160
'Resistance to some (lipophilic) antifolates has been associated with P-glycoprotein (P-gp)-mediated multidrug resistance (MDR). A possible relationship with non-P-gp MDR has not been established. We studied resistance to antifolates in SW-1573 human lung carcinoma cells, a P-gp overexpressing variant SW-1573/2R160 and a multidrug resistance protein (MRP) overexpressing variant SW-1573/2R120. In
Down-regulation of topoisomerase II by camptothecin does not prevent additive activity of the topoisomerase II inhibitor etoposide in vitro.
Journal:Anticancer Drugs
PubMed ID:9311443
'Topoisomerases (Topo) I and II are cellular enzymes that catalyze the relaxation of topologically strained DNA and that are involved in a number of DNA-related processes. Their complete inhibition by Topo I and II inhibitors gives promise for improvements in the treatment of malignant diseases. However, preclinical studies showed down-regulation
Evidence for uptake of vital dye by activated rat peritoneal mast cells: an in vitro imaging study.
Journal:Neuroimage
PubMed ID:9343581
'Uptake of material from surrounding medium by activated rat peritoneal mast cells (PMCs) was studied using in vitro peritoneal eluate cells, the vital fluorescent dye sulforhodamine B (SFRM-B), secretagogue compound 48/80, and an imaging technique. PMCs, which undergo different states of degranulation, are shown to possess the ability to take
Toxicity of organic fluorophores used in molecular imaging: literature review.
Journal:Mol Imaging
PubMed ID:20003892
'Fluorophores are potentially useful for in vivo cancer diagnosis. Using relatively inexpensive and portable equipment, optical imaging with fluorophores permits real-time detection of cancer. However, fluorophores can be toxic and must be investigated before they can be administered safely to patients. A review of published literature on the toxicity of
Growth inhibition of human glioma cells induced by 8-chloroadenosine, an active metabolite of 8-chloro cyclic adenosine 3':5'-monophosphate.
Journal:Cancer Res
PubMed ID:1617676
'8-Chloroadenosine 3'':5''-monophosphate (8ClcAMP) inhibits the growth of human glioma cell lines at much lower concentrations than more commonly used cyclic AMP analogues, without inducing morphological differentiation. The mechanism by which 8ClcAMP exerts this effect is not fully understood. We examined whether the growth-inhibitory effect of this compound is due to