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Citations & References (22)
Invitrogen™
Pacific Blue™ Succinimidyl Ester
アミン反応性Pacific Blue™スクシンイミジルエステルは、ブルーダイオード（バイオレット）レーザーの405 nmスペクトルラインにより約410/455の最大励起／最大発光を持つ青色蛍光バイオコンジュゲートの作成に使用できます。すべてのPacific Blue™色素製品を表示。フルオロフォアセレクションガイドを表示。詳細を見る
| 製品番号（カタログ番号） | 数量 |
|---|---|
| P10163 | 5 mg |
製品番号（カタログ番号） P10163
価格（JPY）お問い合わせください ›
47,100
キャンペーン価格
Ends: 27-Mar-2026
78,500割引額 31,400 (40%)
Each
数量:
5 mg
アミン反応性Pacific Blue™スクシンイミジルエステルは、ブルーダイオード（バイオレット）レーザーの405 nmスペクトルラインにより約410/455の最大励起／最大発光を持つ青色蛍光バイオコンジュゲートの作成に使用できます。
すべてのPacific Blue™色素製品を表示。
フルオロフォアセレクションガイドを表示。
すべてのPacific Blue™色素製品を表示。
フルオロフォアセレクションガイドを表示。
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
検出法蛍光
発光451
励起416
フローサイトメーターレーザーライン405
フォーマット固体
標識または色素Pacific Blue™
製品タイプスクシンイミジルエステル
数量5 mg
反応性部分活性エステル、スクシンイミジルエステル
出荷条件室温
溶解性DMSO(ジメチルスルホキシド)
標識タイプPacific色素
製品ラインPacific Blue
Unit SizeEach
組成および保存条件
1バイアル(1 mg)入りです。 フリーザー(-5∼-30度)に保存し、遮光してください。
引用および参考文献 (22)
引用および参考文献
Abstract
Tyramide signal amplification for analysis of kinase activity by intracellular flow cytometry.
Journal:Cytometry A
PubMed ID:20824632
'Intracellular flow cytometry permits quantitation of diverse molecular targets at the single-cell level. However, limitations in detection sensitivity inherently restrict the method, sometimes resulting in the inability to measure proteins of very low abundance or to differentiate cells expressing subtly different protein concentrations. To improve these measurements, an enzymatic amplification
Reduction in muscle fibre number during the adaptive radiation of notothenioid fishes: a phylogenetic perspective.
Journal:J Exp Biol
PubMed ID:12819266
'The fish fauna of the continental shelf of the Southern Ocean is dominated by a single sub-order of Perciformes, the Notothenioidei, which have unusually large diameter skeletal muscle fibres. We tested the hypothesis that in fast myotomal muscle a high maximum fibre diameter (FD(max)) was related to a reduction in
Cytoskeletal-assisted dynamics of the mitochondrial reticulum in living cells.
Journal:Proc Natl Acad Sci U S A
PubMed ID:12417764
'Subcellular organelle dynamics are strongly influenced by interactions with cytoskeletal filaments and their associated motor proteins, and lead to complex multiexponential relaxations that occur over a wide range of spatial and temporal scales. Here we report spatio-temporal measurements of the fluctuations of the mitochondrial reticulum in osteosarcoma cells by using
High-content single-cell drug screening with phosphospecific flow cytometry.
Journal:Nat Chem Biol
PubMed ID:18157122
'Drug screening is often limited to cell-free assays involving purified enzymes, but it is arguably best applied against systems that represent disease states or complex physiological cellular networks. Here, we describe a high-content, cell-based drug discovery platform based on phosphospecific flow cytometry, or phosphoflow, that enabled screening for inhibitors against
Fluorescent cell barcoding in flow cytometry allows high-throughput drug screening and signaling profiling.
Journal:Nat Methods
PubMed ID:16628206
'Flow cytometry allows high-content, multiparameter analysis of single cells, making it a promising tool for drug discovery and profiling of intracellular signaling. To add high-throughput capacity to flow cytometry, we developed a cell-based multiplexing technique called fluorescent cell barcoding (FCB). In FCB, each sample is labeled with a different signature,