The largest database of trusted experimental protocols

Urea nitrogen test

Manufactured by EKF Diagnostics
Sourced in United States

The Urea Nitrogen Test is a laboratory diagnostic device used to measure the concentration of urea nitrogen in a patient's blood sample. It provides a quantitative analysis of the urea nitrogen levels, which is a key indicator of kidney function and nitrogen metabolism.

Automatically generated - may contain errors

5 protocols using urea nitrogen test

1

Liver MPS Functional Characterization

Check if the same lab product or an alternative is used in the 5 most similar protocols
Perfusion of the liver MPS was initiated 2 days after loading to allow recovery and spreading of the hiPSC-Heps. Media was collected every two days and analyzed for albumin and urea secretion. Albumin was measured using an enzyme-linked immunosorbent assay (Bethyl Laboratories). Urea nitrogen was measured using a colorimetric assay (urea nitrogen test, Stanbio Laboratory) modified to be performed in a 384-well microtiter plate, including increase in the incubation time of reactants from 60 to 90 min at 60°C prior to reading. All the biochemical assays were performed in 10 µL of media and measured on a SpectraMax i3 plate reader (Molecular Devices). All the sample results were calculated by interpolation of sample raw values from standard curves performed in parallel. The same assays were repeated for conventional cell cultures of hiPSC-Heps.
+ Open protocol
+ Expand
2

Quantitative Biochemical Assays for Cell Efflux

Check if the same lab product or an alternative is used in the 5 most similar protocols
Albumin was measured using an enzyme linked immunosorbent assay (Bethyl Laboratories, Montgomery, TX, USA). LDH (CytoTox 96, Promega, Madison, WI, USA) and urea nitrogen (Urea Nitrogen Test, Stanbio Laboratory) was measured using colorimetric assays. Human TNF-α chemi-luminescent ELISA was performed as described by manufacturer guidelines (ThermoFisher, Pittsburgh, PA, USA). All biochemical assays performed on the efflux media were performed in 384 well microplates according to manufacturer's instructions with the exception of the blood urea nitrogen (BUN) assay, which was modified from the manufacturer's protocol by reconfiguring for a 384 well microtiter plate and increasing the incubation of reactants from 60 to 90 min at 60° C before reading. All biochemical assays were conducted on 10 μL of media for each readout and measured on a SpectraMax M2 (Molecular Devices, Sunnyvale, CA, USA) microtiter plate reader. All sample results were calculated by interpolation of sample values from standard curves performed in parallel.
+ Open protocol
+ Expand
3

Biochemical Assays for Organ-on-Chip Research

Check if the same lab product or an alternative is used in the 5 most similar protocols
Albumin, urea, LDH and TNF-α were measure as previously reported.17 The albumin ELISA kit was purchased from Bethyl Laboratories (Montgomery TX), the LDH CytoTox 96 kit from ProMega (Madison, WI), urea nitrogen test from StanBio Laboratory (Boerne, TX) and human TNF-α from ThermoFisher Scientific (Waltham, MA). Urea nitrogen, LDH and the TNF-α assays require 10 μL of media each per sample per time point. The assays were conducted following the manufacturer's guidelines with the exception of the urea nitrogen test, which was reconfigured to a 384 well format.17 ,18 The albumin ELISA measurement was determined from 1 μl of media per sample per time point following the manufacture's instructions. All media efflux assay measurements were collected with the SpectraMax M2 (Molecular Devices, Sunnyvale CA) microtiter plate reader. A Data Import Tool (DIT) was used to process raw data from biochemical assays and format the processed data for uploading into the MPS-Db. The DIT is designed to process raw data using a logistic, polynomial or linear regression algorithm to best fit the standard curve for calculating test sample results and format the processed data for uploading into the MPS-Db. For the studies reported here, the logistic regression fit was used.
+ Open protocol
+ Expand
4

Plasma Analysis of Metabolites

Check if the same lab product or an alternative is used in the 5 most similar protocols
Blood samples were collected 4 to 6 h after feeding on the last day of each period by puncture of a coccygeal vessel into vacutainers containing sodium heparin (BD Diagnostics, Franklin Lakes, NJ). Plasma was separated by centrifugation at 2,000 × g for 15 min at 4°C and analyzed for urea N (Urea Nitrogen Test, reference no. 0580-250; Stanbio Laboratory Inc., Boerne, TX), glucose (Glucose Test C, reference no. 439-90901; Wako Chemicals USA Inc., Richmond, VA), and nonesterified fatty acids (NEFA; HR Series NEFA-HR 1, reference no. Wako Chemicals USA Inc.) .
+ Open protocol
+ Expand
5

Plasma Metabolite Analysis in Livestock

Check if the same lab product or an alternative is used in the 5 most similar protocols
Blood samples were collected on the last day of each period by puncture of a coccygeal vessel into Vacutainers containing sodium heparin (BD Diagnostics, Franklin Lakes, NJ). Plasma was separated by centrifugation at 2,000 × g for 15 min at 4°C and analyzed for urea nitrogen (Urea Nitrogen Test, reference no. 0580-250; Stanbio Laboratory Inc., Boerne, TX), glucose (Glucose Test C, reference no. 439-90901; Wako Chemicals USA Inc., Richmond, VA), BHB (procedure no. 2440; Stanbio Laboratory Inc.), and fatty acids (HR Series NEFA-HR 1, reference no. Wako Chemicals USA Inc. ). An aliquot (5 mL) of plasma was shipped on dry ice to Virginia Tech University (Blacksburg) and analyzed for AA and α-aminoadipic acid following the methods of Burrin et al. (1995) .
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!