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Citations & References (25)
Invitrogen™
6-ROX (6-Carboxy-X-Rhodamine), single isomer
カルボキシルローダミン6G（CR 6G）の励起スペクトルおよび発光スペクトルは、フルオレセインとテトラメチルローダミンの励起スペクトルとの間にあります。525 nmでのピーク吸収により、カルボキシルローダミン6Gの接合は、アルゴンイオンレーザーの514 nmスペクトルラインに最適です詳細を見る
| 製品番号（カタログ番号） | 数量 |
|---|---|
| C6156 または、製品番号C-6156 | 10 mg |
製品番号（カタログ番号） C6156
または、製品番号C-6156
価格（JPY）お問い合わせください ›
61,000
Each
数量:
10 mg
カルボキシルローダミン6G（CR 6G）の励起スペクトルおよび発光スペクトルは、フルオレセインとテトラメチルローダミンの励起スペクトルとの間にあります。525 nmでのピーク吸収により、カルボキシルローダミン6Gの接合は、アルゴンイオンレーザーの514 nmスペクトルラインに最適です。アミン反応性6-CR 6G、SEは、この蛍光色素分子をアミン修飾オリゴヌクレオチドなどの生体高分子に結合させるために使用できます。
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
発光525
励起514
標識または色素ROX
製品タイプ6-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 (25)
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
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