INPP5D Kit ELISA
Aperçu rapide pour INPP5D Kit ELISA (ABIN6218880)
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Méthode de détection
Type de méthode
Gamme de detection
Application
Type d'échantillon
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Seuil minimal de détection
- 1.56 ng/mL
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Analytical Method
- Quantitative
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Sensibilité
- < 0.88 ng/mL
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Ingrédients
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The kit components listed are for reference only. The product manual may differ slightly. The product should be used as stated on the product manual included and delivered together with the product.
- Pre-coated 96-Well Microplate
- Standard
- Standard Diluent Buffer
- Wash Buffer
- Detection Reagent A
- Detection Reagent B
- Diluent A
- Diluent B
- TMB Substrate
- Stop Solution
- Plate Sealer
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Matériel non inclus
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- 37 °C incubator
- Multi and single channel pipettes and sterile pipette tips
- Squirt bottle or automated microplate washer
- 1.5 mL tubes
- Distilled water
- Absorbent filter papers
- 100 mL and 1 liter graduated cylinders
- Microplate reader (wavelength: 450 nm)
- ELISA Shaker
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Volume d'échantillon
- 100 µL
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Plaque
- Pre-coated
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Préparation des réactifs
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This procedure is provided for reference only. The product manual may differ slightly. The product should be used as stated on the product manual included and delivered together with the product.
- 1) Standard: Prepare the standard with the recommended volume of Standard Diluent Buffer, to make the standard solution. Then use the Standard Diluent buffer to carry out serial dilutions of the standard solution, as instructed in the Protocol.
- 2) Wash Buffer: Dilute the concentrated Wash Buffer with distilled water, as instructed in the Protocol.
- 3) Detection Reagent Preparation: Calculate the total volume of working solution required. Dilute Detection Reagent A and Detection Reagent B with Diluent A and Diluent B, respectively, at 1:100.
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Procédure de l'essai
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This procedure is provided for reference only. The product manual may differ slightly. The product should be used as stated on the product manual included and delivered together with the product.
- 1) Set standard, test samples and control wells.
- 2) Aliquot 100 μL of diluted standard into the standard wells.
- 3) Aliquot 100 μL of Standard Diluent buffer into control (zero) well.
- 4) Aliquot 100 μL of diluted samples into the sample wells. Incubate for 1 hr at 37 °C.
- 5) Aliquot 100 μL of Detection Reagent A to each well. Incubate for 1 hr at 37 °C.
- 6) Wash 3 times.
- 7) Aliquot 100 μL of Detection Reagent B to each well. Incubate for 30 mins at 37 °C.
- 8) Wash 5 times.
- 9) Aliquot 90 μL of TMB Substrate to each well. Incubate for 10-20 mins at 37 °C.
- 10) Aliquot 50 μL of Stop Solution.
- 11) Measure the OD at 450 nm.
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Calcul des résultats
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For calculation, average the O.D.450 duplicate readings for each reference standard and each sample and substract the average control (zero) O.D.450 reading. The standard curve can be plotted as the relative O.D.450 of each reference standard solution (Y) vs. the respective concentration of each standard solution (X). The INPP5D concentration of the samples can be interpolated from the standard curve.
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Restrictions
- For Research Use only
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Stock
- 4 °C
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Stockage commentaire
- Shipped at 4 °C. Upon receipt, store the kit according to the storage instruction in the kit's manual.The stability of the kit is determined by the rate of activity loss. The loss rate is less than 5% within the expiration date under appropriate storage conditions. To minimize performance fluctuations, operation procedures and lab conditions should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same user throughout.
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Date de péremption
- 6 months
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- INPP5D (Inositol Polyphosphate-5-Phosphatase, 145kDa (INPP5D))
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Autre désignation
- Phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase 1
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UniProt
- P97573
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Pathways
- TCR Signaling, BCR Signaling, L'effet Warburg
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