Background/Introduction: Urea, or carbamide, is the end product of protein nitrogen metabolism and is the primary vehicle for removing toxic ammonia from the body. Urea is synthesized in the liver from the ammonia produced from the catabolism of amino acids via the hepatic urea cycle. The conversion from ammonia to urea is regulated by N-acetylglutamate, which activates carbamoyl phosphate synthetase in the urea cycle. Urea is transported in the blood to the kidneys where it is excreted in the urine. In addition to its role as a carrier of waste nitrogen, urea also has a role in the countercurrent exchange system of the nephrons in which water and ions are re-absorbed from excreted urine. It is freely filtered by the glomeruli and partially passively resorbed as filtrate transverses the renal tubules. Urea reabsorption is inversely proportional to urine flow rate. Consequently, urea concentration depends upon protein intake, protein catabolism, and kidney function. Urea quantitation is one of the most widely applied tests for kidney function evaluation. The analysis of urea in serum, plasma and urine is an important clinical test for renal disease and dysfunction. The test is frequently tested in conjunction with creatinine determination for identification of pre-renal, renal, and post renal uremia. Toxic urea levels are associated with renal, liver, or other system dysfunction. Pre-renal uremia relates to water depletion, increased protein catabolism, infection, hypovolemia, or cardiac decomposition. Glomerulonephritis, tubular necrosis, nephrosclerosis, chronic nephritis, and polycystic kidney are examples of renal uremia, while post renal uremia is predominantly urinary tract obstructions or leakage. Increased urea levels can also be linked to other disease states such as liver disease, diabetes, and congestive heart failure. High plasma urea levels are known as Azotemia. Decreased urea levels are associated with acute hepatic insufficiency or excess parenteral fluid therapy. Urea Assay Kit is based on the Berthelot reaction. Urea is first degraded into ammonia and carbon dioxide, which further reacts with an alkaline developer to produce a blue-green colored product that can be measured with a standard spectrophotometric plate reader at an optical density between 580-630 nm. Each kit provides sufficient reagents to perform up to 200 assays, including blanks, urea standards and unknown samples and controls.
2. Sands, J.M. et al. (2009) Semin Nephrol. 29(3): 178-195.
3. Walker, V. (2009) Diabetes, Obes and Metab. 11(9): 823-835.
4. Young, D.S. et al. (1972) Clin. Chem. 18: 1041-1303.
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Product Notes
The Urea (Catalog #AAA168363) is an Assay Kit and is intended for research purposes only. The product is available for immediate purchase. It is sometimes possible for the material contained within the vial of "Urea, Assay Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.Precautions
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