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P3804

Sigma-Aldrich

o-Phenylendiamin -dihydrochlorid

tablet, 5 mg substrate per tablet

Synonym(e):

1,2-Phenylenediamine tablet, OPD, OPD Tablet

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About This Item

Lineare Formel:
C6H4(NH2)2·2HCl
CAS-Nummer:
615-28-1
Molekulargewicht:
181.06
Beilstein:
3912045
EG-Nummer:
210-418-7
MDL-Nummer:
MFCD00012966
UNSPSC-Code:
12352204
PubChem Substanz-ID:
24898457
NACRES:
NA.83

Qualitätsniveau

200

Form

tablet

mp (Schmelzpunkt)

258 °C (dec.) (lit.)

Löslichkeit

water: 1 tablet/10 mL, clear, colorless

Lagertemp.

2-8°C

SMILES String

Cl[H].Cl[H].Nc1ccccc1N

InChI

1S/C6H8N2.2ClH/c7-5-3-1-2-4-6(5)8;;/h1-4H,7-8H2;2*1H

InChIKey

RIIWUGSYXOBDMC-UHFFFAOYSA-N

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Allgemeine Beschreibung

o-Phenylendiamindihydrochlorid (OPD) ist ein chromogenes Substrat, das in Enzyme-linked-Immunosorbent-Assay(ELISA)-Verfahren eingesetzt werden kann, da es Meerrettichperoxidasekonjugate nutzt. Das Substrat produziert ein lösliches Endprodukt mit orange-brauner Farbe, das bei 450 nm spektrofotometrisch gemessen werden kann. Die OPD-Reaktion kann mit 3 N HCl oder 3 mol/l H2SO4 gestoppt und bei 492 nm gemessen werden.

Anwendung

o-Phenylenediamine dihydrochloride has been used:
  • as a chromogenic substrate in indirect enzyme-linked immunosorbent assay (ELISA) to detect immunoglobin G (IgG) antibodies against certain recombinant antigens/proteins
  • as a streptavidin-horseradish peroxidase (HRP) substrate sandwich ELISA to analyze human interleukin (IL)-17A, IL-23, and IP-10
  • as a substrate in ELISA for determination of IgG-class antibodies to Mycobacterium bovis in serum

Verpackung

16 mg total tablet weight

Rekonstituierung

Dissolve one tablet in 0.05 M phosphate-citrate buffer, pH 5.0, to the desired concentration (typically an OPD concentration of 0.4 mg/ml is used). Add 40 μl of fresh 30% hydrogen peroxide per 100 ml of substrate buffer solution, immediately prior to use. Tablets are individually packaged in foil packets.

Signalwort

Warning

Gefahreneinstufungen

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Irrit. 2 - Muta. 2 - Skin Sens. 1

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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o-Phenylendiamin -dihydrochlorid peroxidase substrate

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H G Marco et al.
Peptides, 21(9), 1313-1321 (2000-11-10)
We have isolated a peptide from extracts of sinus glands from a South African spiny lobster species, Jasus lalandii, by high-performance liquid chromatography (HPLC) and identified it as a putative molt-inhibiting hormone (MIH) by (i) an in vitro assay with
Joanne L Casey et al.
Methods in molecular biology (Clifton, N.J.), 421, 111-124 (2008-10-02)
Large repertoires of peptides displayed on bacteriophage have been extensively used to select for ligand-binding molecules. This is a relatively straightforward process involving several cycles of selection against target molecules, and the resulting ligands can be tailored to various applications.
Cassandra Koole et al.
The Journal of pharmacology and experimental therapeutics, 353(1), 52-63 (2015-01-30)
The glucagon-like peptide-1 receptor (GLP-1R) is a class B G protein-coupled receptor that has a critical role in the regulation of glucose homeostasis, principally through the regulation of insulin secretion. The receptor system is highly complex, able to be activated
Florian Krammer et al.
Clinical and vaccine immunology : CVI, 21(8), 1153-1163 (2014-06-20)
Emerging H7N9 influenza virus infections in Asia have once more spurred the development of effective prepandemic H7 vaccines. However, many vaccines based on avian influenza viruses--including H7--are poorly immunogenic, as measured by traditional correlates of protection. Here we reevaluated sera
Sarah L Rowland et al.
The Journal of experimental medicine, 211(10), 1977-1991 (2014-09-03)
Plasmacytoid dendritic cells (pDCs) have long been implicated in the pathogenesis of lupus. However, this conclusion has been largely based on a correlative link between the copious production of IFN-α/β by pDCs and the IFN-α/β "signature" often seen in human
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