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引用和文献 (23)
Invitrogen™
5-ROX（5-羧基-X-罗丹明，三乙基铵盐），单异构体
5-ROX 羧酸用于寡核苷酸标记和自动 DNA 测序应用。该染料的偶联物光谱波长比 Lisaamine™ 罗丹明 B 偶联物光谱的波长更长，但比 Texas了解更多信息
| 货号 | 数量 |
|---|---|
| C6124 | 10 mg |
货号 C6124
价格（CNY)
4,669.00
Each
数量:
10 mg
价格（CNY)
4,669.00
Each
5-ROX 羧酸用于寡核苷酸标记和自动 DNA 测序应用。该染料的偶联物光谱波长比 Lisaamine™ 罗丹明 B 偶联物光谱的波长更长，但比 Texas Red™ 偶联物光谱波长稍短。
仅供科研使用。不可用于诊断程序。
规格
化学反应性胺
标签或染料ROX
产品类型5-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 (23)
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
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
Localization, physiology, and modulation of a molluskan dopaminergic synapse.
Journal:J Neurobiol
PubMed ID:9298763
'We investigated the location, physiology, and modulation of an identified synapse from the central nervous system (CNS) of the mollusk Lymnaea stagnalis. Specifically, the excitatory synapse from interneuron right pedal dorsal one (RPeD1) to neurons visceral dorsal two and three (VD2/3) was examined. The gross and fine morphology of these