During electrophoresis the temperature of the first sample and the reference sample is changed by an amount sufficient to change an electrophoretic mobility of at least one of the first or reference polynucleotides.
The first sample and a reference sample are subjected to electrophoresis in the presence of at least one intercalating dye.
The methods involve determining the amount of folate receptor alpha in a sample derived from a subject and comparing this level with the level of folate receptor alpha in a control sample or reference sample.
A sample of the cell suspension is retained as a negative control sample.
A control sample comprising the first sample and a redox probe is exposed to the liposomes.
Inclusion of a negative control sample is optional.
A control including the microorganism in the diluent is also prepared.
Provided is an analyzer which can perform analysis of a reagent blank by using an optimal blank sample for each item of analysis without increasing the time being spent for analysis of a reagent blank.
The test includes comparing amounts and sizes of red blood cells, leukocytes and/or platelets in a control sample and at least one test sample.
A sample from the patient is provided, and the level of oviduct-specific glycoprotein (OGP) in the sample is determined and compared to a control sample.
A detecting system is provided for testing a control sample and a sample of the fluid from the fluid line.
The kit comprises a control sample and a product sample, where each of the sample comprises a set of super absorbent polymer beads.
One specimen shall be stored in a dark and dry container for subsequent use as reference unexposed specimen.
A control sample is run and analyzed to generate an exclusion list of unwanted sample components.
A second aliquot of said sample functions as a control sample, in which protein components are labelled with a different, mono functional dye.
Then, a limited sampling of the sensors is tested for accuracy using a control sample.
limit of detection means the output signal or concentration value above which it can be affirmed, with a stated level of confidence that a sample is different from a blank sample containing no determinand of interest
With this method, to evaluate protein expression of a disease or a drug treated sample in comparison with a control sample, two converse collaborative labeling experiments are performed in parallel.
As apparatus and method for assessing colour fastness involves the use of digital imaging means to capture an image of a test sample and a control sample.
A test agent contained in a test sample in which parkin ligase activity exceeds the ligase activity in said control sample is identified as a candidate compound for treatment of Parkinson's Disease.