p-Nitrophenyl Phosphate

Description

• General description: p-Nitrophenyl phosphate is the most common substrate for alkaline phosphatase-based ELISA assays. Hydrolysis of the phosphate ester liberates p-nitrophenol, a soluble, yellow chromogen that can be measured spectrophotometrically at 405 nm (ε = 1.83 x 104 M-1cm-1). As the reaction is linear, kinetic assays can be performed. Endpoint determinations can also be performed by stopping the reaction with strong base and measuring the absorbance at 405 nm. This p-NPP preparation is a stable, convenient, liquid concentrate in a proprietary solvent.
• Application: ELISA
• Biochem/physiol Actions: Primary TargetSubstrate for alkaline phosphatase-based ELISA assays
• Warning: Toxicity: Standard Handling (A)
• Physical form: Supplied as a 50X concentrate.
• Reconstitution: Discard if solution turns bright yellow or becomes turbid.
• Other Notes: Functionality check performed on the final product in ELISA.Suggested procedure for use of p-NPP in alkaline phosphatase-based ELISAs:1. Prepare 1X p-NPP Substrate Solution: To 39 parts dH2O add 1 part 50X p-NPP Concentrate and 10 parts p-NPP Substrate Buffer (Cat. No. 487664). Mix well and store protected from light. This diluted reagent is suitable for up to 10 h after preparation.Note: Cat. No. 487664 is an AMP (2-amino-2-methyl-1-propanol)-based buffer. Other buffers, e.g. diethanolamine (DEA)-based and 2-amino-2-methyl-1,3-propanediol (AMPD)-based, may also be employed.2. Complete all required incubations with antibodies and alkaline phosphatase-labeled probes.3. Wash plate wells at least 4 times with Tris-buffered saline (TBS) containing 0.1% Tween®-20 detergent. DO NOT USE PHOSPHATE BUFFERS; inorganic phosphate is a potent inhibitor of alkaline phosphatase.4. After the final wash, shake and blot all residual buffer from the wells. 5. Add 100 µl of 1X p-NPP Substrate Solution (prepared in Step 2) to each well and incubate for 15-60 min. (If a kinetic study is desired, readings at 405 nm may be taken at intermediate intervals).[Note: Optimal incubation times may vary depending on the amount of enzyme present. If color develops too quickly, dilution of the probe, antibody, or alkaline phosphatase-labeled reagent may be required.]6. Stop the reaction by adding 100 µl 1 N NaOH. 7. Read absorbance at 405 nm.Note: Variations in time, reagent volumes, and temperature may require further standardization by the user.
• Legal Information: CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany