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Citations & References (23)
Invitrogen™
5-ROX (5-Carboxy-X-Rhodamine, Triethylammonium Salt), single isomer
5-ROX（5-カルボキシ-X-ローダミン、トリエチルアンモニウム塩）、単一異性体
| 製品番号（カタログ番号） | 数量 |
|---|---|
| C6124 | 10 mg |
製品番号（カタログ番号） C6124
価格（JPY）
38,000
キャンペーン価格
Ends: 25-Dec-2026
63,400割引額 25,400 (40%)
Each
数量:
10 mg
The carboxylic acid of 5-ROX is used for oligonucleotide labeling and automated DNA sequencing applications. Conjugates of this dye have longer-wavelength spectra than the spectra of Lisaamine™ rhodamine B conjugates, but somewhat shorter-wavelength spectra than those of Texas Red™ conjugates.
5-ROXのカルボン酸は、オリゴヌクレオチドラベリングおよび自動DNAシーケンシングアプリケーションに使用されます。この色素の接合は、Lisaamine™ローダミンB接合のスペクトルよりも長い波長スペクトルを有しますが、テキサスレッド™接合のスペクトルよりも若干短い波長スペクトルを有します。
研究用にのみ使用できます。診断用には使用いただけません。
仕様
化学反応性アミン
標識または色素ROX
製品タイプ5-ROX
数量10 mg
反応性部分カルボン酸
出荷条件室温
標識タイプ従来の色素
Unit SizeEach
組成および保存条件
フリーザー(-5∼-30度)に保存し、遮光してください。
よくあるご質問（FAQ）
What is the excitation and emission wavelength for rhodamine?
引用および参考文献 (23)
引用および参考文献
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