Rat Urea transporter 1, SLC14A1 CLIA KIT
96 Tests
Operating instruction
FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE BEGINNING!
Synonyms
SLC14A1,SLC14A1 JK; HUT11; HsT1341; RACH1; RACH2; UT-B1; UT1; UTE; UT-B,UT11,UT3,urea transporter member 1; urea transporter JK glycoprotein; urea transporter erythrocyte; urea transporter-B1; solute carrier family 14 member 1, Urea transporter 1
Search name
Rat SLC14A1 CLIA KIT ,Rat SLC14A1 JK CLIA KIT ,Rat HUT11 CLIA KIT ,Rat HsT1341 CLIA KIT ,Rat RACH1 CLIA KIT ,Rat RACH2 CLIA KIT ,Rat UT-B1 CLIA KIT ,Rat UT1 CLIA KIT ,Rat UTE CLIA KIT ,Rat UT-B CLIA KIT ,Rat UT11 CLIA KIT ,Rat UT3 CLIA KIT ,Rat urea transporter member 1 CLIA KIT ,Rat urea transporter JK glycoprotein CLIA KIT ,Rat urea transporter erythrocyte CLIA KIT ,Rat urea transporter-B1 CLIA KIT ,Rat solute carrier family 14 member 1 CLIA KIT ,Rat Urea transporter 1 CLIA KIT
Intended use
This chemiluminescenceimmunoassay kit allows for the in vitro quantitative determination of Rat Urea transporter 1 concentrations in serum, plasma, tissue homogenates, cell culture supernates, and other biological fluids.
Test principle
The microtiter plate provided in this kit has been pre-coated with an antibody specific to Urea transporter 1. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated monoclonal antibody preparation specific forUrea transporter 1 and Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a luminol substrate solution is added to each well. Only those wells that contain Urea transporter 1, biotin-conjugated antibody and enzyme-conjugated Avidin will emission wavelength of radiation 425nm (max)chemiluminescence by HRP catalyzed.The concentration of Urea transporter 1 in the samples was positively correlated with the light value. Luminosity is determined bymicroplate chemiluminescence analyzer(RLU.S-1.PW-1). The concentration of Urea transporter 1 in the samples is then determined by comparing the light value of the samples to the standard curve.
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