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Merck

A9941

Sigma-Aldrich

Ácido 2,2′-acino-bis(3-etilbenzotiazolina-6-sulfónico) diammonium salt

chromogenic, tablet

Sinónimos:

AzBTS-(NH4)2, Diamonio del 2,2′-acino-bis(3-etilbenzotiazolina-6-sulfonato)

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About This Item

Fórmula empírica (notación de Hill):
C18H24N6O6S4
Número de CAS:
Peso molecular:
548.68
Beilstein/REAXYS Number:
7329461
EC Number:
MDL number:
UNSPSC Code:
12352204
PubChem Substance ID:
NACRES:
NA.21

product name

Ácido 2,2′-acino-bis(3-etilbenzotiazolina-6-sulfónico) diammonium salt, tablet, 10 mg substrate per tablet

form

tablet

solubility

deionized water: 100 mL

storage temp.

room temp

SMILES string

[NH4+].[NH4+].CCN1C(\Sc2cc(ccc12)S([O-])(=O)=O)=N\N=C3/Sc4cc(ccc4N3CC)S([O-])(=O)=O

InChI

1S/C18H18N4O6S4.2H3N/c1-3-21-13-7-5-11(31(23,24)25)9-15(13)29-17(21)19-20-18-22(4-2)14-8-6-12(32(26,27)28)10-16(14)30-18;;/h5-10H,3-4H2,1-2H3,(H,23,24,25)(H,26,27,28);2*1H3/b19-17-,20-18-;;

InChI key

OHDRQQURAXLVGJ-AXMZSLBLSA-N

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General description

ABTS mainly used in ELISA (enzyme-linked immunosorbent assay) procedures.
ABTS, 2,2′-Azino-bis(3-ethylbenzthiazoline-6-sulfonic acid), is a chromogenic substrate used:
  • For a reaction with laccase or bilirubin oxidase
  • For a reaction with peroxidase enzymes: (like HRP for example). ABTS in combination with hydrogen peroxide
A peroxidase reaction of ABTS in the presence of hydrogen peroxide produces a green soluble end product which can be read spectrophotometrically at 405nm. The reaction may be stopped with 1% sodium dodecyl sulfate (SDS).
ABTS, 2,2′-Azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt is light sensitive, and water soluble chemical compound

Application

  • 2,2′-Azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt, ABTS, has been used as a substrate in ELISA (enzyme-linked immunosorbent assay).†
  • ABTS is also used to measure glucose concentrations in different solutions including blood serum.
  • The food industry uses ABTS to measure the antioxidant capacities within different foods.
  • Since it is less readily oxidized than TMB and OPD substrates, ABTS is less sensitive for ELISA applications. Thus ABTS has some advantageous over TMB and OPD in cases of large background results
  • It is recommended for ELISA (microwell) procedures, not recommended for membrane applications.
El ácido 2,2′-acino-bis(3-etilbenzotiazolina-6-sulfónico es un sustrato de la peroxidasa adecuado para procedimientos ELISA. Este sustrato rinde un producto final soluble que es de color verde y puede leerse espectrofotométricamente a 405 nm. La reacción puede pararse con dodecilsulfatosódico (SDS) al 1 %. Recomendado para procedimientos ELISA (micropocillo), no recomendado para aplicaciones con membrana.

Reconstitution

Dissolve 1 tablet in 100 ml of 0.05 M phosphate-citrate buffer, pH 5.0 (Tablets available as Sigma Product No. P4809). Add 25 μl of fresh 30% hydrogen peroxide

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Visite la Librería de documentos

B Porstmann et al.
Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie, 19(7), 435-439 (1981-07-01)
o-Phenylenediamine, 2,2'-azino-di(3-ethylbenzthiazoline sulphonic acid-6) (ABTS), o-dianisidine and 4-aminoantipyrine were compared as chromogens for the determination of horseradish peroxidase. Highest sensitivity in the determination of horseradish peroxidase-IgG conjugates in dissolved form was obtained with o-phenylenediamine. When these conjugates were used in
Vignesh Narayanaswamy et al.
Breastfeeding medicine : the official journal of the Academy of Breastfeeding Medicine, 16(12), 987-994 (2021-08-13)
Objective: To evaluate the immune response to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in colostrum from women who tested positive for the virus. Methods: Between March and September 2020 we obtained bilateral colostrum samples collected on spot cards within
Development of a feline proinsulin immunoradiometric assay and a feline proinsulin enzyme-linked immunosorbent assay (ELISA): A novel application to examine beta cell function in cats
Kley S, et al.
Domestic Animal Endocrinology, 311-318 (2008)
Da Di et al.
Pathogens (Basel, Switzerland), 10(8) (2021-08-29)
The SARS-CoV-2 nucleocapsid protein (N) binds a single-stranded viral RNA genome to form a helical ribonucleoprotein complex that is packaged into virion particles. N is relatively conserved among coronaviruses and consists of the N-terminal domain (NTD) and C-terminal domain (CTD)
Collaborative study on a guinea pig serological method for the assay of acellular pertussis vaccines
Winsnes R, et al.
Pharmeuropa Bio & Scientific Notes, 19-32 (2009)

Artículos

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NBT-BCIP substrate system aids in western blotting and immunohistological staining, producing a blue-purple insoluble end product.

NBT-BCIP substrate system aids in western blotting and immunohistological staining, producing a blue-purple insoluble end product.

NBT-BCIP substrate system aids in western blotting and immunohistological staining, producing a blue-purple insoluble end product.

Protocolos

To measure alcohol oxidase activity, this assay uses 2,2′-azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) and a continuous spectrophotometric rate determination at 405 nm.

To measure alcohol oxidase activity, this assay uses 2,2′-azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) and a continuous spectrophotometric rate determination at 405 nm.

To measure alcohol oxidase activity, this assay uses 2,2′-azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) and a continuous spectrophotometric rate determination at 405 nm.

To measure alcohol oxidase activity, this assay uses 2,2′-azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) and a continuous spectrophotometric rate determination at 405 nm.

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