Quanticon™ Rat S100B(S100 Calcium Binding Protein B) ELISA Kit

Quanticon™ Rat S100B(S100 Calcium Binding Protein B) ELISA Kit

Principle of the Procedure

The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat S100B. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat S100B. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat S100B, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 Rat S100B in the samples is then determined by comparing the OD of the samples to the standard curve.

Cat no: ABQK-ES96-S100Brt
ABQK-ES96-S100Brt
Size: Rate
Rate
96T: $450
$450
48T: $230
$230

Product Name

Quanticon™ Rat S100B(S100 Calcium Binding Protein B) ELISA Kit

SKU

ABQK-ES96-S100Brt

Applications

ELISA

Reactivity

Rat

Alternative Name

S100-B, NEF, S100Beta, S-100 protein subunit beta

Standard

2000pg/mL.

Sensitivity

13.1pg/mL

Detection Range

31.2-2000pg/mL.

Sample Type

Serum, Plasma, Tissue homogenate, Urine, Saliva, Cerebrospinal fluid (CSF), Cell culture supernatant and Other biological samples

Sample Volume

100 ÎĽL

Assay Type

Sandwich

Assay Duration

3.5 H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations   

Quanticon™ Rat S100B(S100 Calcium Binding Protein B) ELISA Kit

Quanticon™ Rat S100B(S100 Calcium Binding Protein B) ELISA Kit

Quanticon™ Rat S100B(S100 Calcium Binding Protein B) ELISA Kit

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Principle of the Procedure

The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat S100B. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat S100B. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat S100B, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 Rat S100B in the samples is then determined by comparing the OD of the samples to the standard curve.

Cat no: ABQK-ES96-S100Brt ABQK-ES96-S100Brt Size: Rate Rate 96T: $450 $450 48T: $230 $230 Datasheet Get Quote MS/DS COA

Product Name

Quanticon™ Rat S100B(S100 Calcium Binding Protein B) ELISA Kit

SKU

ABQK-ES96-S100Brt

Applications

ELISA

Reactivity

Rat

Alternative Name

S100-B, NEF, S100Beta, S-100 protein subunit beta

Standard

2000pg/mL.

Sensitivity

13.1pg/mL

Detection Range

31.2-2000pg/mL.

Sample Type

Serum, Plasma, Tissue homogenate, Urine, Saliva, Cerebrospinal fluid (CSF), Cell culture supernatant and Other biological samples

Sample Volume

100 ÎĽL

Assay Type

Sandwich

Assay Duration

3.5 H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

 

Citations   

Product Name

Quanticon™ Rat S100B(S100 Calcium Binding Protein B) ELISA Kit

SKU

ABQK-ES96-S100Brt

Applications

ELISA

Reactivity

Rat

Alternative Name

S100-B, NEF, S100Beta, S-100 protein subunit beta

Standard

2000pg/mL.

Sensitivity

13.1pg/mL

Detection Range

31.2-2000pg/mL.

Sample Type

Serum, Plasma, Tissue homogenate, Urine, Saliva, Cerebrospinal fluid (CSF), Cell culture supernatant and Other biological samples

Sample Volume

100 ÎĽL

Assay Type

Sandwich

Assay Duration

3.5 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