Quanticon™ Nitrofuran Furazolidone (AOZ) ELISA Kit

Quanticon™ Nitrofuran Furazolidone (AOZ) ELISA Kit

Quanticon™ Nitrofuran Furazolidone (AOZ) ELISA Kit

Principle of the Procedure        

This assay employs the competitive inhibition enzyme immunoassay technique. The kit consists of an enzyme-labeled plate pre-coated with coupled antigens, horseradish enzyme markers, antibodies, standard substances, and other supporting reagents. During detection, standard substances or sample solutions are added. AOZ in the samples competes with the pre-coated coupled antigens on the enzyme-labeled plate for AOZ antibody. After adding the enzyme markers, TMB substrate is used for color development. The absorbance value of the sample is negatively correlated with the content of AOZ it contains, and the residual amount of AOZ in the sample can be obtained by comparing with the standard curve.

Cat no: ABQF-EC96-AOZge
ABQF-EC96-AOZge
Size: Rate
Rate
96T: $450
$450
48T: $230
$230

Product Name

Quanticon™ Nitrofuran Furazolidone (AOZ) ELISA Kit

SKU

ABQF-EC96-AOZge

Applications

ELISA

Reactivity

General

Standard

4.05 ppb

Sensitivity

0.05 ppb (ng/mL)

Detection Range

0.05 ppb~4.05 ppb

Sample Type

Milk, Milk Powder & Egg Powder, Honey, Muscle (Livestock, Fish, Shrimp), Cooked Food

Sample Volume

50 ÎĽL

Assay Type

Competitive

Assay Duration

1 H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations   

Quanticon™ Nitrofuran Furazolidone (AOZ) ELISA Kit

Quanticon™ Nitrofuran Furazolidone (AOZ) ELISA Kit

Quanticon™ Nitrofuran Furazolidone (AOZ) ELISA Kit

elisa-kit-images-e1737629308569-removebg-preview
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Principle of the Procedure        

This assay employs the competitive inhibition enzyme immunoassay technique. The kit consists of an enzyme-labeled plate pre-coated with coupled antigens, horseradish enzyme markers, antibodies, standard substances, and other supporting reagents. During detection, standard substances or sample solutions are added. AOZ in the samples competes with the pre-coated coupled antigens on the enzyme-labeled plate for AOZ antibody. After adding the enzyme markers, TMB substrate is used for color development. The absorbance value of the sample is negatively correlated with the content of AOZ it contains, and the residual amount of AOZ in the sample can be obtained by comparing with the standard curve.

Cat no: ABQF-EC96-AOZge ABQF-EC96-AOZge Size: Rate Rate 96T: $450 $450 48T: $230 $230 Datasheet Get Quote MS/DS COA

Product Name

Quanticon™ Nitrofuran Furazolidone (AOZ) ELISA Kit

SKU

ABQF-EC96-AOZge

Applications

ELISA

Reactivity

General

Standard

4.05 ppb

Sensitivity

0.05 ppb (ng/mL)

Detection Range

0.05 ppb~4.05 ppb

Sample Type

Milk, Milk Powder & Egg Powder, Honey, Muscle (Livestock, Fish, Shrimp), Cooked Food

Sample Volume

50 ÎĽL

Assay Type

Competitive

Assay Duration

1 H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations   

Product Name

Quanticon™ Nitrofuran Furazolidone (AOZ) ELISA Kit

SKU

ABQF-EC96-AOZge

Applications

ELISA

Reactivity

General

Standard

4.05 ppb

Sensitivity

0.05 ppb (ng/mL)

Detection Range

0.05 ppb~4.05 ppb

Sample Type

Milk, Milk Powder & Egg Powder, Honey, Muscle (Livestock, Fish, Shrimp), Cooked Food

Sample Volume

50 ÎĽL

Assay Type

Competitive

Assay Duration

1 H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations   

Principle of the Procedure

This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Pig CCK. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Pig CCK. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Pig CCK in the samples is then determined by comparing the OD of the samples to the standard curve.

Citations  Â