Pacific Orange™ Succinimidyl Ester, Triethylammonium Salt
Citas y referencias (7)
Invitrogen™
Pacific Orange™ Succinimidyl Ester, Triethylammonium Salt
El succinimidilo éster Pacific Orange™ es un colorante excitable con luz violeta (405 nm) con una emisión máxima de ∼551Más información
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Número de catálogo
Cantidad
P30253
1 mg
Número de catálogo P30253
Precio (CLP)
-
Cantidad:
1 mg
El succinimidilo éster Pacific Orange™ es un colorante excitable con luz violeta (405 nm) con una emisión máxima de ∼551 nm. Esto permite su uso con otros fluoróforos excitables de violeta, como el colorante Pacific Blue™, para el análisis de multiparámetros utilizando una única fuente de excitación. Como clase de compuestos, las formas de éster de succinimidil proporcionan la química de reacción más eficiente y fácil de usar para vincular selectivamente un colorante a grupos de aminas primarias accesibles en proteínas, ácidos nucleicos modificados u otras biomoléculas. Los ésteres de succinimidil son reactivos excelentes para la modificación de aminas porque los enlaces covalentes que forman son tan estables como los enlaces peptídicos utilizados para enlazar aminoácidos en proteínas. El éster de succinimidil Pacific Orange™ se suministra como 1 mg de polvo seco y debe ser almacenado a ≤ - 20 °C, desecado, y protegido de la luz.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Almacenar en el congelador (de – 5 a – 30 °C) y proteger de la luz.
Citations & References (7)
Citations & References
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.
'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