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Merck

P6140

Peroxidase from horseradish

Type X, ammonium sulfate suspension

Synonim(y):

Donor:hydrogen-peroxide oxidoreductase, Horseradish peroxidase

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2000 UNITS

395,00 zł

5000 UNITS

693,00 zł

25000 UNITS

2510,00 zł

395,00 zł


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Informacje o tej pozycji

Numer CAS:
eCl@ss:
32160410
UNSPSC Code:
12352204
NACRES:
NA.54
EC Number:
232-668-6
MDL number:
Specific activity:
≥225 units/mg protein (biuret, using pyrogallol)
Biological source:
horseradish
Concentration:
≥1.0 mg/mL

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Pozwól nam pomóc

SMILES string

[O+H2]O[O-]

InChI key

JSPLKZUTYZBBKA-UHFFFAOYSA-N

InChI

1S/H2O3/c1-3-2/h1-2H

biological source

horseradish

type

Type X

form

ammonium sulfate suspension

specific activity

≥225 units/mg protein (biuret, using pyrogallol)

mol wt

~44 kDa

concentration

≥1.0 mg/mL

absorbance ratio

RZ 2.5-3.5

storage temp.

2-8°C

Quality Level

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Ta pozycja
P8125P6782P8415
specific activity

≥225 units/mg protein (biuret, using pyrogallol)

specific activity

≥50 units/mg solid (using pyrogallol)

specific activity

≥250 units/mg solid (using pyrogallol), 950-2000 units/mg solid (using ABTS)

specific activity

≥250 units/mg solid (using pyrogallol)

biological source

horseradish

biological source

-

biological source

-

biological source

-

form

ammonium sulfate suspension

form

essentially salt-free, lyophilized powder

form

essentially salt-free, lyophilized powder

form

essentially salt-free, lyophilized powder

concentration

≥1.0 mg/mL

concentration

-

concentration

-

concentration

-

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

mol wt

~44 kDa

mol wt

~44 kDa

mol wt

~44 kDa

mol wt

~44 kDa

General description

Horseradish peroxidase is isolated from horseradish roots (Amoracia rusticana) and belongs to the ferroprotoporphyrin group of peroxidases. HRP is a single chain polypeptide containing four disulfide bridges. It is a glycoprotein containing 18% carbohydrate. The carbohydrate composition consists of galactose, arabinose, xylose, fucose, mannose, mannosamine, and galactosamine depending upon the specific isozyme. Its molecular weight (~44 kDa) includes the polypeptide chain (33,890 Daltons), hemin plus Ca2+ (~700 Daltons), and carbohydrate (~9,400 Daltons). At least seven isozymes of HRP exist. The isoelectric point for horseradish peroxidase isozymes ranges from 3.0 - 9.0.

Application

Horseradish peroxidase (HRP) is isolated from horseradish roots (Amoracia rusticana). It is used in biochemistry applications such as western blots, ELISA and Immunohistochemistry. Horseradish peroxidase is used to amplify a weak signal and increase detectability of a target molecule, such as a protein[1]. Product P6140 has been used to detect low density lipoprotein (LDL)[2].
The enzyme from Sigma has been used while assessing the skin sensitization potential of pro-haptens.[3] It has also been used to show that peroxidase (PO) activity and its heat stability correlate with the availability of free Ca2+ ions.[4]

Biochem/physiol Actions

When incubated with a substrate, horseradish peroxidase produces a coloured, fluorimetric, or luminescent derivative of the labeled molecule, allowing quantification[1]. Horseradish peroxidase has been shown to slightly reduce the level of inhibition in a cydAB mutant[5].
HRP readily combines with hydrogen peroxide (H2O2) and the resultant [HRP-H2O2] complex can oxidize a wide variety of hydrogen donors. The optimal pH is 6.0-6.5 and the enzyme is most stable in the pH range of 5.0-9.0. HRP can be conjugated to antibodies by several different methods that include the use of glutaraldehyde, periodate oxidation, disulfide bonds, and also via amino- and thiol-directed cross-linkers. It is smaller and more stable than the enzyme labels, β-galactosidase and alkaline phosphatase. Hence, it is the most desired label. Also, its glycosylation leads to lower non-specific binding. It is also used for the determination of glucose and peroxides in solution. Sodium azide, cyanide, L-cystine, dichromate, ethylenethiourea, hydroxylamine, sulfide, vanadate, p-aminobenzoic acid, and Cd2+, Co2+, Cu2+, Fe3+, Mn2+, Ni2+, Pb2+ ions are found to inhibit its enzyme activity.

Physical form

Crystalline suspension in 3.2 M (NH4)2SO4 solution containing potassium phosphate buffer, pH 6.0

Preparation Note

Water may be used to dilute suspension if needed.

Analysis Note

Preliminary studies indicate the presence of two basic and no acidic isoenzymes
The RZ (Reinheitszahl) is the absorbance ratio A403/A275 determined at 0.5-1.0 mg/ml in deionized water. It is a measure of hemin content, not enzymatic activity. Even preparations with high RZ may have low enzymatic activity.

Other Notes

One pyrogallol unit will form 1.0 mg purpurogallin from pyrogallol in 20 sec at pH 6.0 at 20 °C.
View more information on peroxidase at www.sigma-aldrich.com/enzymeexplorer.
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pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Resp. Sens. 1

Klasa składowania

11 - Combustible Solids

wgk

WGK 1

ppe

Eyeshields, Gloves, type N95 (US)


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Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

David Stuart Thompson et al.
Plants (Basel, Switzerland), 10(7) (2021-07-03)
The extensibility of synthetic polymers is routinely modulated by the addition of lower molecular weight spacing molecules known as plasticizers, and there is some evidence that water may have similar effects on plant cell walls. Furthermore, it appears that changes
Christoph Plieth et al.
Plant signaling & behavior, 7(6), 650-660 (2012-05-15)
In this paper we demonstrate how peroxidase (PO) activities and their heat stability correlate with the availability of free Ca(2+) ions. Calcium ions work as a molecular switch for PO activity and exert a protective function, rendering POs heat stable.
N Santanam et al.
Journal of lipid research, 39(11), 2111-2118 (1998-11-04)
Estradiol has been documented to inhibit the oxidation of low density lipoprotein (LDL). We show that physiological concentrations of estradiol do not inhibit the oxidation of LDL by copper. LDL samples isolated from a) premenopausal and postmenopausal women and from
John W Callahan et al.
Methods in molecular biology (Clifton, N.J.), 347, 321-330 (2006-10-31)
This chapter describes in detail a practical procedure for the preparation of radiolabeled galactocerebroside and its use in the assay of galactocerebrosidase (GalCase), the enzyme deficient in globoid cell leukodystrophy (Krabbe disease). The reference range for leukocytes and fibroblasts is
Y P Chau et al.
Acta anatomica, 153(2), 135-144 (1995-01-01)
Vascular permeability in various rat sympathetic ganglia, including superior cervical ganglia, thoracic ganglia and the celiac-mesenteric ganglia (CMG) complex, was investigated by using lanthanum and horseradish peroxidase (HRP) as tracers with special attention to the neuronal and small granule-containing (SGC)

Produkty

Odkryj naszą peroksydazę z enzymów chrzanowych, produkty, substraty i inhibitory do testów ELISA, testów immunologicznych i zastosowań białkowych.

Discover our peroxidase from horseradish enzymes, products, substrates, and inhibitors for your ELISA, immunoassay, and protein application needs.

Instructions for working with enzymes supplied as ammonium sulfate suspensions

Protokoły

Ta procedura służy do oznaczania aktywności enzymatycznej peroksydazy przy użyciu pirogallolu jako substratu.

Reinheitszahl (RZ) is the ratio of absorbance due to hemin (A403, Soret region) to absorbance due to protein (A275).

This procedure is for the determination of Peroxidase enzymatic activity using Pyrogallol as the substrate.

To standardize a procedure for the assay of Peroxidase using 2,2'-Azino-bis(3-Ethylbenzthiazoline-6-Sulfonic Acid) as a substrate.

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