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Advanced Glycosylation end Products ELISA KIT
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Advanced Glycosylation end Products ELISA KIT
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Advanced Glycosylation end Products ELISA KIT

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País:

China

N º de Modelo:

E01A0002

Precio FOB:

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Persona de contacto tang

hongliu, Shanghai, Shanghai

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Especificaciones del producto

Descripción del producto


INTENDED USE
ThisB.GAGEs ELISA kit is intended Laboratory for Research use only and is not for use in diagnostic or therapeutic procedures. The Stop Solution changes the color from blue to yellow and the intensity of the color is measured at **0nm using a spectrophotometer. In order to measure the concentration of AGEs in the sample, this AGEs ELISA Kit includes a set of calibration standards. The calibration standards are assayed at the same time as the samples and allow the operator to produce a standard curve of Optical Density versus AGEs concentration. The concentration of AGEs in the samples is then determined by comparing the O.D. of the samples to the standard curve.
PRINCIPLE OF THE ASSAY
The coated well immunoenzymatic assay for the quantitative measurement of serum AGEs utilizes a monoclonal anti-AGEs and a AGEs-HRP conjugate. The assay sample and buffer are incubated together with anti-AGEs antibody coated plate for sixty and washed. The diluted AGEs-HRP conjugate is then added to each well and incubated. After the incubation period, the wells are decanted and washed three times. The wells are then incubated with a substrate for the enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stopping solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at **0nm in a microplate reader. The intensity of the color is inversely proportional to the AGEs concentration since AGEs from samples and AGEs-HRP conjugate compete for the anti-AGEs antibody binding site. Since the number of sites is limited, as more sites are occupied by AGEs from the sample, fewer sites are left to bind AGEs-HRPconjugate. Standards of known AGEs concentrations are run concurrently with the samples being assayed and a standard curve is plotted relating the intensity of the color (Optical Density) to the concentration of AGEs. The unknown AGEs
 
 
concentration in each sample is interpolated from this curve.
REAGENTS PROVIDED
All reagents provided are stored at **8° C. Refer to the expiration date on the label.
1.         MICROTITER PLATE *6 wells
2.         ENZYMECONJUGATE 6.0 mL 1 vial
3.         STANDARD.1  0pg/ml  1 vial
4.         STANDARD.2  *0pg/ml  1 vial
5.         STANDARD.3 **0pg/ml  1 vial
6.         STANDARD.4 **0pg/ml  1 vial
7.         STANDARD.5 **0pg/ml  1 vial
8.         STANDARD.6 ***0pg/ml  1 vial
9.         SUBSTRATE A 6.0 mL 1 vial
*0.      SUBSTRATE B 6.0 mL 1 vial
*1.      STOP SOLUTION 6.0 mL 1 vial
*2.      WASH SOLUTION x**0 *0 mL 1 vial
*3.      Instruction   1
 
SAMPLE COLLECTION AND STORAGE
Serum-Use a serum separator tube(SST) and allow samples to clot for *0minutes before centrifugation for *5minutes at approximately ***0xg. Remove serum and assay immediately or aliquot and store samples at **0 °C or **0°C.
Plasma- Collect plasma using EDTA or heparin as an anticoagulant. Centrifuge samples for *5 minutes at ***0 x g at **8°C within *0minutes of collection. Store samples at **0°C or **0°C.Avoid repeated freeze-thaw cycles.
Cell culture fluid and other biological fluids- Remove particulates by centrifugation and assay immediately or aliquot and store samples at **0°C or **0°C.Avoid repeated freeze-thaw cycles.
 
 
NOTE:Serum, plasma, and cell culture fluid samples to be used within 7 days may be stored at **8°C, otherwise samples must stored at **0°C(2months) or **0°C(6months) to avoid loss of bioactivity and contamination. Avoid freeze-thaw cycles .When performing the assay slowly bring samples to room temperature.
DO NOT USE HEAT-TREATED SPECIMENS.
 
MATERIALS REQUIRED BUT NOT SUPPLIED
1.         Microplate reader capable of measuring absorbance at **0 nm.
2.         Precision pipettes to deliver 2 ml to 1 ml volumes.
3.         Adjustable *0ml ***0ml pipettes for reagent preparation.
4.         Adjustable *0ml ***0ml pipettes for reagent preparation.
5.         **0 ml and 1 liter graduated cylinders.
6.         Calibrated adjustable precision pipettes, preferably with disposable plastic tips. (A manifold multi-channel pipette is desirable for large assays.)
7.         Absorbent paper.
8.         *7°C incubator.
9.         Distilled or deionized water.
*0.      Data analysis and graphing software. Graph paper: linear (Cartesian), log-log or semi-log, or log-logit as desired.
*1.      Tubes to prepare standard or sample dilutions.
 
PRECAUTIONS
1.         Do not substitute reagents from one kit lot to another. Standard, conjugate and microtiter plates are matched for optimal performance. Use only the reagents supplied by manufacturer.
2.         Allow kit reagents and materials to reach room temperature (****5°C) before use. Do not use water baths to thaw samples or reagents.
3.         Do not use kit components beyond their expiration date.
 
4.         Use only deionized or distilled water to dilute reagents.
5.         Do not remove microtiter plate from the storage bag until needed. Unused strips should be stored at **8°C in their pouch with the desiccant provided.
6.         Use fresh disposable pipette tips for each transfer to avoid contamination.
7.         Do not mix acid and sodium hypochlorite solutions.
8.         Serum and plasma should be handled as potentially hazardous and capable of transmitting disease. Disposable gloves must be worn during the assay procedure, since no known test method can offer complete assurance that products derived from human blood will not transmit infectious agents. Therefore, all blood derivatives should be considered potentially infectious and good laboratory practices should be followed.
9.         All samples should be disposed of in a manner that will inactivate viruses.
*0.      Solid Waste: Autoclave *0 min. at **1°C.
*1.      Liquid Waste: Add sodium hypochlorite to a final concentration of 1.0%. The waste should be allowed to stand for a minimum of *0 minutes to inactivate the viruses before disposal.
*2.      Substrate Solution is easily contaminated. If bluish prior to use,do not use

País: China
N º de Modelo: E01A0002
Precio FOB: Obtener el precio más reciente
Lugar de origen: -
Precio de pedido mínimo: -
Cantidad de pedido mínimo: -
Detalle de embalaje: -
El tiempo de entrega: -
Capacidad de suministro: -
Tipo de pago: -
Grupo de productos : Shanghai Bluegene Biotech

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