-
-
Overview
-
Key Features
· Highly accurate and sensitive. Quantitation limit is 330 nM for NAD+ in whole blood measured in two 96-well plate assays.
· Easy to handle. One step metabolite extraction is followed by separate measurement of NAD+ in the extract. Detection time is less than 10 minutes.
· High throughput. Can be easily adopted into high-throughput 96-well plate assay to analyze hundreds of samples per day.
Principals
The principle of the assay is a cyclic enzymatic reaction with a colorimetric end-point detection. First, NAD+ is extracted from a blood sample in a single step. After this NAD+ is stabilized and measured.
Reagents Provided
Extraction BUFFER A, NAD+ stabilizing reagent, NAD+ standard stock, Assay BUFFER C, Assay color reagent, Enzyme, Stop solution, Positive control
Kit Requires
Multi-channel pipets. Two clear-bottom 96-well plates suitable for colorimetric assays, heat block with adjustable temperature (up to 80°C), spectrophotometric plate reader
Precautions and Warnings
· For research use only by trained personnel.
· The Stop Solution may cause skin, eye, and respiratory irritation. Avoid breathing in fumes.
· Assay color reagent may cause skin irritation. Handle with care, use gloves.
· BUFFER A can cause eye irritation. Handle with care, use googles.Please contact us at for specific academic pricing.
-
- Properties
-
Overview