Pacific Orange™ Succinimidyl Ester, Triethylammonium Salt
Pacific Orange™ Succinimidyl Ester, Triethylammonium Salt
Invitrogen™

Pacific Orange™ Succinimidyl Ester, Triethylammonium Salt

Pacific Orange™スクシンイミジルエステルは、紫光励起性(405 nm)、最大発光波長約551 nmの蛍光色素です。このため、Pacific詳細を見る
製品番号(カタログ番号)数量
P302531 mg
製品番号(カタログ番号) P30253
価格(JPY)
36,200
Online offer
Ends: 27-Mar-2026
60,400
割引額 24,200 (40%)
Each
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数量:
1 mg

Pacific Orange™スクシンイミジルエステルは、紫光励起性(405 nm)、最大発光波長約551 nmの蛍光色素です。このため、Pacific Blue™色素など、紫光励起性の他の蛍光色素分子と併用して、単一の励起光源を使用したマルチパラメーター分析が可能になります。化合物の1クラスであるスクシンイミジルエステル型は、非常に効率的で使いやすい反応化学により、タンパク質、修飾核酸、またはその他の生体分子上のアクセス可能な一級アミン基に対し、色素を選択的に結合します。スクシンイミジルエステルは、タンパク質中のアミノ酸結合に使用されるペプチド結合と同等の安定性を持つ共有結合を形成するため、アミン修飾用の優れた試薬となります。Pacific Orange™スクシンイミジルエステルは1 mgの乾燥粉末として提供されます。乾燥状態で、≤-20℃で遮光して保管してください。

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551
励起405
標識または色素Pacific Orange™
製品タイプスクシンイミジルエステル
数量1 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
標識タイプPacific色素
製品ラインPacific Orange
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。

引用および参考文献 (7)

引用および参考文献
Abstract
Dual channel STED nanoscopy of lytic granules on actin filaments in natural killer cells.
Authors:Mace EM, Orange JS,
Journal:Commun Integr Biol
PubMed ID:22808328
Natural killer (NK) cells are innate immune effectors that eliminate diseased and tumorigenic targets through the directed secretion of specialized secretory lysosomes, termed lytic granules. This directed secretion is triggered following the formation of an immunological synapse (IS), which is characterized by actin re-modeling and receptor organization at the interface ... More
Tyramide signal amplification for analysis of kinase activity by intracellular flow cytometry.
Authors:Clutter MR, Heffner GC, Krutzik PO, Sachen KL, Nolan GP,
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 ... More
Dual receptor T cells mediate pathologic alloreactivity in patients with acute graft-versus-host disease.
Authors:Morris GP, Uy GL, Donermeyer D, Dipersio JF, Allen PM,
Journal:
PubMed ID:23740900
Acute graft-versus-host disease (aGVHD) results from a robust response of donor T cells transferred during hematopoietic stem cell transplantation (HSCT) to allogeneic peptide-major histocompatibility complex antigens. Previous investigations have not identified T cell subsets that selectively mediate either protective immunity or pathogenic alloreactivity. We demonstrate that the small subset of ... More
Activation of T lymphocytes in atherosclerotic plaques.
Authors:Grivel JC, Ivanova O, Pinegina N, Blank PS, Shpektor A, Margolis LB, Vasilieva E,
Journal:Arterioscler Thromb Vasc Biol
PubMed ID:21960562
To decipher the immunologic mechanisms of plaque maturation and rupture, it is necessary to analyze the phenotypes and distribution of individual lymphocytes that migrate to the plaques, as well as their activation at different stages of plaque formation. We developed a protocol to isolate plaque-residing immune cells and analyze their ... More
In vivo functional analysis and genetic modification of in vitro-derived mouse neutrophils.
Authors:McDonald JU, Cortini A, Rosas M, Fossati-Jimack L, Ling GS, Lewis KJ, Dewitt S, Liddiard K, Brown GD, Jones SA, Hallett MB, Botto M, Taylor PR,
Journal:FASEB J
PubMed ID:21368104
Mature neutrophils are notoriously short-lived immune cells that cannot be genetically manipulated. Analysis of gene function therefore requires genetically modified animals, which is expensive, time-consuming, and costly in animal life. Analysis of gene function in neutrophils in a physiologically relevant context thus represents a significant problem in the field. We ... More