{"id":8100,"date":"2023-03-09T17:24:30","date_gmt":"2023-03-09T23:24:30","guid":{"rendered":"https:\/\/nuevo22.cidsamexico.com\/?post_type=al_product&p=8100"},"modified":"2023-03-09T17:56:05","modified_gmt":"2023-03-09T23:56:05","slug":"luminol-3-aminophthalhydrazide","status":"publish","type":"al_product","link":"https:\/\/nuevo22.cidsamexico.com\/index.php\/productos\/luminol-3-aminophthalhydrazide\/","title":{"rendered":"Luminol [3-Aminophthalhydrazide]\u00a0"},"content":{"rendered":"\n

Luminol [3-aminoftalhidrazida] es un sustrato de peroxidasa luminiscente. Para exhibir su luminiscencia, el luminol debe activarse con un oxidante. HRP cataliza la descomposici\u00f3n del per\u00f3xido de hidr\u00f3geno. <\/p>\n\n\n\n

Cuando el luminol reacciona con el ion hidr\u00f3xido, se forma un diani\u00f3n. El ox\u00edgeno producido a partir del per\u00f3xido de hidr\u00f3geno luego reacciona con el diani\u00f3n de luminol. El producto de esta reacci\u00f3n, un per\u00f3xido org\u00e1nico, es muy inestable y se produce por la p\u00e9rdida de nitr\u00f3geno, el cambio de electrones del estado excitado al estado fundamental y la emisi\u00f3n de energ\u00eda en forma de fot\u00f3n. Esta emisi\u00f3n produce el resplandor azul.<\/p>\n\n\n\n

<\/div>\n\n\n\n
Catalogo<\/th>Producto<\/th>Presentaci\u00f3n<\/th><\/tr><\/thead>
AAT-11050<\/td>Luminol [3-Aminophthalhydrazide] *CAS 521-31-3*<\/td>1 gr<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n
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\"pdf\"\/<\/figure>\n\n\n\n

SDS<\/a><\/p>\n\n\n\n

\"pdf\"\/<\/figure>\n\n\n\n

Protocol<\/a><\/p>\n<\/div>\n\n\n\n

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Importante, Solo para uso en investigaci\u00f3n (RUO). Almacenamiento: Congelaci\u00f3n a <-15\u00a0\u00b0C. MInimizar la exposici\u00f3n a la luz.<\/p>\n\n\n\n

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Propiedades Fisicas<\/mark><\/p>\n\n\n\n

Peso Molecular<\/td>177.16<\/td><\/tr>
Disolvente<\/td>DMSO<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n
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Calculadora<\/mark><\/p>\n\n\n\n

Preparaci\u00f3n de la soluci\u00f3n de stock com\u00fan<\/strong>
Volumen de DMSO necesario para reconstituir la masa espec\u00edfica de Luminol [3-aminoftalhidrazida] CAS 521-31-3<\/em> a la concentraci\u00f3n dada. Tenga en cuenta que el volumen es solo para preparar la soluci\u00f3n madre. Consulte el protocolo experimental de muestra para conocer los buffers experimentales\/fisiol\u00f3gicos apropiados.<\/p>\n\n\n\n

<\/td>0.1 mg<\/strong><\/td>0.5 mg<\/strong><\/td>1 mg<\/strong><\/td>5 mg<\/strong><\/td>10 mg<\/strong><\/td><\/tr>
1 mM<\/strong><\/td>564.462 \u00b5L<\/td>2.822 mL<\/td>5.645 mL<\/td>28.223 mL<\/td>56.446 mL<\/td><\/tr>
5 mM<\/strong><\/td>112.892 \u00b5L<\/td>564.462 \u00b5L<\/td>1.129 mL<\/td>5.645 mL<\/td>11.289 mL<\/td><\/tr>
10 mM<\/strong><\/td>56.446 \u00b5L<\/td>282.231 \u00b5L<\/td>564.462 \u00b5L<\/td>2.822 mL<\/td>5.645 mL<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n
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Espectro<\/mark><\/p>\n\n\n\n

Abrir en Advanced Spectrum Viewer<\/a><\/em><\/p>\n\n\n\n

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Propiedades Espectrales<\/mark><\/p>\n\n\n\n

Excitaci\u00f3n (nm)<\/td>355<\/td><\/tr>
Emision (nm)<\/td>412<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n
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Imagen<\/mark><\/p>\n\n\n\n

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Figura 1. <\/strong>Estructura quimica para Luminol [3-Aminophthalhydrazide] *CAS 521-31-3*<\/p>\n\n\n\n

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Bibliograf\u00eda<\/mark><\/p>\n\n\n\n

Linker histone H1. 2 and H1. 4 affect the neutrophil lineage determination<\/a>
Authors: <\/strong>Sollberger, Gabriel and Streeck, Robert and Apel, Falko and Caffrey, Brian Edward and Skoultchi, Arthur I and Zychlinsky, Arturo
Journal: <\/strong>Elife (2020): e52563<\/p>\n\n\n\n

Transaldolase 1 is required for Neutrophil Extracellular Trap (NET) Formation<\/a>
Authors: <\/strong>Morath, Jakob Paul
Journal: <\/strong>(2020)<\/p>\n\n\n\n

Linker Histone H1 subtypes specifically regulate neutrophil differentiation
Authors: <\/strong>Sollberger, Gabriel and Streeck, Robert and Caffrey, Brian Edward and Zychlinsky, Arturo
Journal: <\/strong>bioRxiv (2019): 763482<\/p>\n\n\n\n

Gasdermin D plays a vital role in the generation of neutrophil extracellular traps<\/a>
Authors: <\/strong>Sollberger, Gabriel and Choidas, Axel and Burn, Garth Lawrence and Habenberger, Peter and Di Lucrezia, Raffaella and Kordes, Susanne and Menninger, Sascha and Eickhoff, Jan and Nussbaumer, Peter and Klebl, Bert and others,
Journal: <\/strong>Science immunology (2018): eaar6689<\/p>\n\n\n\n

<\/div>\n\n\n\n

Referencias<\/mark><\/p>\n\n\n\n

Ver todas las 14 referencias:\u00a0Citation Explorer<\/a><\/em><\/p>\n\n\n\n

Luminol-hydrogen peroxide chemiluminescence produced by sweet potato peroxidase
Authors: <\/strong>Alpeeva IS, Yu Sakharov I.
Journal: <\/strong>Luminescence. (2006)<\/p>\n\n\n\n

Ultrasensitive assay of azithromycin in medicine and bio-fluids based on its enhanced luminol-H(2)O(2) chemiluminescence reaction using flow injection technique
Authors: <\/strong>Song Z, Wang C.
Journal: <\/strong>Bioorg Med Chem (2003): 5375<\/p>\n\n\n\n

Application of an enhanced luminol chemiluminescence reaction using 4-[4,5-di(2-pyridyl)-1H-imidazol-2-yl]phenylboronic acid to photographic detection of horseradish peroxidase on a membrane
Authors: <\/strong>Kuroda N, Murasaki N, Wada M, Nakashima K.
Journal: <\/strong>Luminescence (2001): 167<\/p>\n\n\n\n

Comparative studies of the chemiluminescent horseradish peroxidase-catalysed peroxidation of acridan (GZ-11) and luminol reactions: effect of pH and scavengers of reactive oxygen species on the light intensity of these systems
Authors: <\/strong>Osman AM, Zomer G, Laane C, Hilhorst R.
Journal: <\/strong>Luminescence (2000): 189<\/p>\n\n\n\n

New phenylboronic acid derivatives as enhancers of the luminol-H(2)O(2)-horseradish peroxidase chemiluminescence reaction
Authors: <\/strong>Kuroda N, Kawazoe K, Nakano H, Wada M, Nakashima K.
Journal: <\/strong>Luminescence (1999): 361<\/p>\n\n\n\n

What do we measure with luminol-, lucigenin- and penicillin-amplified chemiluminescence? 1. Investigations with hydrogen peroxide and sodium hypochlorite
Authors: <\/strong>Rost M, Karge E, Klinger W.
Journal: <\/strong>J Biolumin Chemilumin (1998): 355<\/p>\n\n\n\n

Enhancer effect of fluorescein on the luminol-H2O2-horseradish peroxidase chemiluminescence: energy transfer process
Authors: <\/strong>Navas Diaz A, Gonzalez Garcia JA, Lovillo J.
Journal: <\/strong>J Biolumin Chemilumin (1997): 199<\/p>\n\n\n\n

Synthesis and characterization of 4-iodophenylboronic acid: a new enhancer for the horseradish peroxidase-catalyzed chemiluminescent oxidation of luminol
Authors: <\/strong>Kricka LJ, Cooper M, Ji X.
Journal: <\/strong>Anal Biochem (1996): 119<\/p>\n\n\n\n

Assay of cholinesterase using a pro-enhancer of the luminol-H2O2-horseradish peroxidase reaction
Authors: <\/strong>Navas Diaz A, Garcia Sanchez F, Gonzalez Garcia JA, Bracho Del Rio V.
Journal: <\/strong>J Biolumin Chemilumin (1995): 285<\/p>\n\n\n\n

4-Phenylylboronic acid: a new type of enhancer for the horseradish peroxidase catalysed chemiluminescent oxidation of luminol
Authors: <\/strong>Kricka LJ, Ji X.
Journal: <\/strong>J Biolumin Chemilumin (1995): 49<\/p>\n\n\n\n

<\/div>\n\n\n\n

Application notes <\/mark><\/p>\n\n\n\n

A Meta-Analysis of Common Calcium Indicator<\/a>s<\/a>
A <\/a>New Protein Crosslinking Method for Labeling and Modifying Antibod<\/a>ies<\/a>
A <\/a>Novel Fluorescent Probe for Imaging and Detecting Hydroxyl Radical in Living Ce<\/a>lls<\/a>
A<\/a>bbreviation of Common Chemical Compounds Related to Peptides<\/a>
Annexin V<\/a><\/p>\n\n\n\n

<\/div>\n\n\n\n

FAQ<\/mark><\/p>\n\n\n\n

What is enhanced chemiluminescence?<\/a>
Are there any alternatives to BrdU (Bromodeoxyuridine)?<\/a>
Are there any alternatives to Cy5?<\/a>
Are there any alternatives to indocyanine green (ICG)?<\/a>
Can DAPI bind to RNA?<\/a><\/p>\n\n\n\n

<\/div>\n\n\n\n

AssayWise <\/mark><\/p>\n\n\n\n

Selecting the right ROS probe<\/a>
HRP Antibody Labeling Using Buccutite\u2122 Crosslinking Technology<\/a>
iFluor\u00ae 700 Dyes<\/a>
Hydroxyl Radical Detection<\/a>
Peroxidase Detection<\/a><\/p>\n\n\n\n

<\/div>\n","protected":false},"excerpt":{"rendered":"

Luminol catalogo 11050 es un sustrato de peroxidasa luminiscente.<\/p>\n","protected":false},"featured_media":8102,"template":"","al_product-cat":[34],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/nuevo22.cidsamexico.com\/index.php\/wp-json\/wp\/v2\/al_product\/8100"}],"collection":[{"href":"https:\/\/nuevo22.cidsamexico.com\/index.php\/wp-json\/wp\/v2\/al_product"}],"about":[{"href":"https:\/\/nuevo22.cidsamexico.com\/index.php\/wp-json\/wp\/v2\/types\/al_product"}],"version-history":[{"count":2,"href":"https:\/\/nuevo22.cidsamexico.com\/index.php\/wp-json\/wp\/v2\/al_product\/8100\/revisions"}],"predecessor-version":[{"id":8104,"href":"https:\/\/nuevo22.cidsamexico.com\/index.php\/wp-json\/wp\/v2\/al_product\/8100\/revisions\/8104"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/nuevo22.cidsamexico.com\/index.php\/wp-json\/wp\/v2\/media\/8102"}],"wp:attachment":[{"href":"https:\/\/nuevo22.cidsamexico.com\/index.php\/wp-json\/wp\/v2\/media?parent=8100"}],"wp:term":[{"taxonomy":"al_product-cat","embeddable":true,"href":"https:\/\/nuevo22.cidsamexico.com\/index.php\/wp-json\/wp\/v2\/al_product-cat?post=8100"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}