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Key Documents

11684302001

Roche

ABTS Solution

solution (ready-to-use), suitable for ELISA

Synonyme(s) :

ABTS Solution, ABTS

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About This Item

Code UNSPSC :
12352204

Forme

solution (ready-to-use)

Niveau de qualité

Utilisation

sufficient for 1,500-3,000 assays (ELISA)

Conditionnement

pkg of 3 × 100 mL

Fabricant/nom de marque

Roche

Technique(s)

ELISA: suitable

Température de stockage

2-8°C

Description générale

ABTS Solution is a ready to use substrate for peroxidase-driven indicator reactions. It contains 2,2-azino-di-[3-ethylbenzthiazoline sulfonate (6)] and H2O2 in glycin/citric acid buffer and is available in slightly green color.

Application

ABTS Solution is a chromogenic substrate for peroxidase in ELISA assays.

Actions biochimiques/physiologiques

2,2′-azino-di-(3-ethylbenzthiazoline sulfonic acid) or ABTS acts a substrate for HRP (horseradish peroxidase) conjugate during enzyme-linked immunosorbent assay (ELISA). It is the most sensitive, and stable substrate when compared to three other substrates namely, 5-aminosalicylic acid (5AS), O-phenylenediamine (OPD), O-tolidine (OT). It also produces the best visual results, where it gives a bluish-green color. ELISA using ABTS is a highly sensitive, specific and reproducible technique This solution is an excellent substrate for enzyme immunoassays with horseradish peroxidase as a marker enzyme.

Forme physique

Reaction product:
Color: green
Evaluation: photometric (405nm)

Remarque sur l'analyse

Absorption: ABTS absorption spectrum reference must always be measured and is determined by a spectrum. The Reference wavelength of 490 nm or higher should be selected due to no measureable absorption. The Reference absorption is usually automatically subtracted by the Plate Reader (background).

Autres remarques

For life science research only. Not for use in diagnostic procedures.

Informations légales

ABTS is a trademark of Roche

Classe de danger pour l'eau (WGK)

nwg

Point d'éclair (°F)

does not flash

Point d'éclair (°C)

does not flash


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Consulter la Bibliothèque de documents

Gang Chen et al.
Biomolecules, 11(10) (2021-10-24)
Most recently, a technology termed TRIM-Away has allowed acute and rapid destruction of endogenous target proteins in cultured cells using specific antibodies and endogenous/exogenous tripartite motif 21 (TRIM21). However, the relatively large size of the full-size mAbs (150 kDa) results
Yuanyuan Kuang et al.
EBioMedicine, 57, 102825-102825 (2020-06-20)
Numerous currently incurable human diseases have been causally linked to mutations in connexin (Cx) genes. In several instances, pathological mutations generate abnormally active Cx hemichannels, referred to also as "leaky" hemichannels. The goal of this study was to assay the
Sylvia Herter et al.
Molecular cancer therapeutics, 12(10), 2031-2042 (2013-07-23)
We report the first preclinical in vitro and in vivo comparison of GA101 (obinutuzumab), a novel glycoengineered type II CD20 monoclonal antibody, with rituximab and ofatumumab, the two currently approved type I CD20 antibodies. The three antibodies were compared in
H Matsuda et al.
The Japanese journal of experimental medicine, 54(3), 131-138 (1984-06-01)
A micro-technique of enzyme-linked immunosorbent assay (ELISA) using ABTS, 2,2'-azino-di-(3-ethylbenzthiazoline sulfonic acid), as a substrate for horseradish peroxidase (HRP) conjugate was studied. In a comparative study among 4 substrates, namely; 5-aminosalicylic acid (5AS), O-phenylenediamine (OPD), O-tolidine (OT) and ABTS, for
Monica Musiani et al.
Nature protocols, 2(10), 2502-2510 (2007-10-20)
PCR is an established technique providing rapid and highly productive amplification of specific DNA sequences. The demand for equally rapid, sensitive and objective methods to achieve detection of PCR products has led to the coupling of PCR with ELISA. PCR-ELISA

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