PDP Kit ELISA
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- Antigène Voir toutes PDP Kits ELISA
- PDP (Pyruvate Dehydrogenase Phosphatase (PDP))
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Reactivité
- Humain
- Méthode de détection
- Colorimetric
- Type de méthode
- Sandwich ELISA
- Gamme de detection
- 0.312 ng/mL - 20 ng/mL
- Seuil minimal de détection
- 0.312 ng/mL
- Application
- ELISA
- Fonction
- The kit is a sandwich enzyme immunoassay for the in vitro quantitative measurement of PDP in human tissue homogenates, cell lysates and other biological fluids.
- Type d'échantillon
- Cell Lysate, Tissue Homogenate
- Analytical Method
- Quantitative
- Specificité
- This assay has high sensitivity and excellent specificity for detection of this index.
- Réactivité croisée (Details)
- No significant cross-reactivity or interference between this index and analogues was observed. Note: Limited by current skills and knowledge, it is impossible for us to complete the cross- reactivity detection between this index and all the analogues, therefore, cross reaction may still exist.
- Sensibilité
- 0.099 ng/mL
- Ingrédients
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- Pre-coated, ready to use 96-well strip plate
- Standard (freeze dried)
- Standard Diluent
- Detection Reagent A
- Detection Reagent B
- Assay Diluent A
- Assay Diluent B
- TMB
- Stop Solution
- Wash Buffer (30X)
- Plate sealer for 96 wells
- Instruction manual
- Matériel non inclus
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- Microplate reader with 450 ± 10nm filter.
- Precision single or multi-channel pipettes and disposable tips.
- Eppendorf Tubes for diluting samples.
- Deionized or distilled water.
- Absorbent paper for blotting the microtiter plate.
- Container for Wash Solution.
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- Volume d'échantillon
- 100 μL
- Durée du test
- 1 - 4.5 h
- Plaque
- Pre-coated
- Protocole
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1. Prepare all reagents, samples and standards
2. Add 100µL standard or sample to each well. Incubate 2 hours at 37°C
3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C
4. Aspirate and wash 3 times
5. Add 100µL prepared Detection Reagent B. Incubate 1 hour at 37°C
6. Aspirate and wash 5 times
7. Add 90µL Substrate Solution. Incubate 15-25 minutes at 37°C
8. Add 50µL Stop Solution. Read at 450nm immediately. - Procédure de l'essai
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The microtiter plate provided in this kit has been pre-coated with an antibody specific to the index. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific to the index. 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 the index, 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 the index in the samples is then determined by comparing the O.D. of the samples to the standard curve.
- Précision du teste
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- Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level the index were tested 20 times on one plate, respectively.
- Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level the index were tested on 3 different plates, 8 replicates in each plate.
- CV(%) = SD/meanX100
- Intra-assay: CV<10%
- Inter-assay: CV<12%
- Restrictions
- For Research Use only
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- Précaution d'utilisation
- The Stop Solution suggested for use with this kit is an acid solution. Wear eye, hand, face, and clothing protection when using this material.
- Conseil sur la manipulation
- The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5 % within the expiration date under appropriate storage conditions. Note: To minimize unnecessary influences on the performance, operation procedures and lab conditions, especially room temperature, air humidity and incubator temperatures should be strictly regulated. It is also strongly suggested that the whole assay is performed by the same experimenter from the beginning to the end.
- Stock
- 4 °C,-20 °C
- Stockage commentaire
- The Assay Plate, Standard, Detection Reagent A and Detection Reagent B should be stored at -20°C upon being received. After receiving the kit , Substrate should be always stored at 4°C.Other reagents are kept according to the labels on vials. But for long term storage, please keep the whole kit at -20°C. The unused strips should be kept in a sealed bag with the desiccant provided to minimize exposure to damp air. The test kit may be used throughout the expiration date of the kit (six months from the date of manufacture). Opened test kits will remain stable until the expiring date shown, provided it is stored as prescribed above.
- Date de péremption
- 12 months
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- Antigène Voir toutes PDP Kits ELISA
- PDP (Pyruvate Dehydrogenase Phosphatase (PDP))
- Autre désignation
- PDP (PDP Produits)
- Synonymes
- 153332_at Kit ELISA, CG12151 Kit ELISA, Dmel\\CG12151 Kit ELISA, PDP Kit ELISA, pdp Kit ELISA, PDH Kit ELISA, PDPC Kit ELISA, PPM2C Kit ELISA, Gm1024 Kit ELISA, Ppm2c Kit ELISA, im:7157162 Kit ELISA, zgc:174908 Kit ELISA, pdp1 Kit ELISA, ppm2c Kit ELISA, Pyruvate dehydrogenase phosphatase Kit ELISA, pyruvate dehydrogenase [acetyl-transferring]-phosphatase 1, mitochondrial Kit ELISA, pyruvate dehyrogenase phosphatase catalytic subunit 1 Kit ELISA, pyruvate dehyrogenase phosphatase catalytic subunit 1 L homeolog Kit ELISA, Pdp Kit ELISA, LOC413080 Kit ELISA, PDP1 Kit ELISA, Pdp1 Kit ELISA, pdp1 Kit ELISA, pdp1.L Kit ELISA
- Sujet
- Alternative name: PDP1, PDH, PPM2C, Protein Phosphatase 2C Magnesium-Dependent Catalytic Subunit, Pyruvate Dehyrogenase Phosphatase Catalytic Subunit 1
- ID gène
- 54704
- UniProt
- Q9P0J1
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