Test ID: UREDF
Reducing Substance, Feces
Method Description 
Describes how the test is performed and provides a method-specific reference
The Clinitest tablet contains cupric sulfate, citric acid, sodium bicarbonate, and anhydrous sodium hydroxide. The test is a qualitative, nonspecific test for the presence of reducing substances in stool. This test utilizes the ability of sugars to reduce cupric to cuprous ions in the presence of heat and alkali, causing a color change from blue to green to orange depending on the amount of reducing substance present.(Package insert: Bayer Clinitest Reagent Tablets. Bayer Corporation, Elkhart, IN)
Day(s) and Time(s) Test Performed Outlines the days and times the test is performed. This field reflects the day and time the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time required before the test is performed. Some tests are listed as continuously performed, which means assays are performed several times during the day.
Monday through Friday
Analytic Time Defines the amount of time it takes the laboratory to setup and perform the test. This is defined in number of days. The shortest interval of time expressed is "same day/1 day," which means the results may be available the same day that the sample is received in the testing laboratory. One day means results are available 1 day after the sample is received in the laboratory.
1 day
Maximum Laboratory Time Defines the maximum time from specimen receipt at Mayo Medical Laboratories until the release of the test result
3 days
Specimen Retention Time Outlines the length of time after testing that a specimen is kept in the laboratory before it is discarded
7 days
Performing Laboratory Location The location of the laboratory that performs the test
Rochester
External
link
PDF
document
Excel
document
Word
document