When haemoglobin undergoes oxygenation, it changes colour, and this is what gives arterial blood its bright red colour. Since the absorption spectra of oxyhaemoglobin and deoxyhaemoglobin differ, the same concentration of a sample of haemoglobin can give different absorption readings depending on the degree of oxygenation. It is therefore necessary to convery haemoglobin into the stable non-oxygen binding form cyanmethaemoglobin before an accurate measurement can be made by spectrophotometric assay pooooo
No, assay by mass balance and assay by as is basis are not equivalent. Assay by mass balance calculates the amount of a component based on material balance equations, while assay by as is basis measures the amount of a component without accounting for any changes or losses that may occur during processing.
An icteric sample can be corrected by using a method that does not rely on colorimetric detection, such as turbidimetric or refractometric methods. Hemolysis can be corrected by using a spectrophotometric method that measures protein concentration at a wavelength where hemoglobin absorption is minimal. Lipemia can be corrected by using ultracentrifugation or filtration to remove the lipids before analyzing the sample for total protein.
An assay is a scientific test or analysis used to measure the presence, amount, or activity of a substance or compound in a sample. Assays are commonly used in biology, chemistry, and medicine to study a wide range of biological and chemical processes.
You can assay thrombin potency by measuring its ability to convert fibrinogen to fibrin, typically using a chromogenic or clot-based assay. The results are compared to a standard curve to determine the potency of the thrombin sample.
assay on as is basis includes the sample+water content+residual solvents+others. but assay on as is basis takes water content into account that means weight of the water present in the sample will be added in weighing the sample quantity of API required.
an assay that measures the appearance or disappearance of a fluorescent.
spectro assay of serratiopeptidase
In the spectrophotometric assay for protein quantification, the method typically detects tyrosine, tryptophan, and cysteine residues due to their absorption at specific wavelengths. These amino acids have distinct absorption spectra that enable the measurement of protein concentration based on the amount of light absorbed.
The procedures for carrying out spectrophotometric and fluorometric GUS assays are similar in that they both involve measuring the enzymatic activity of the GUS enzyme, but they differ in the detection method. In the spectrophotometric assay, absorbance changes at a specific wavelength are measured, while the fluorometric assay measures fluorescence emitted from a substrate after the GUS enzyme acts on it. Additionally, the sensitivity and specific conditions for each assay may vary, influencing the choice of method based on the experimental requirements.
A particular wavelength used for particular spectrophotometric assays is based upon the absorbance pecularity of the substance in consideration/used for the assay. That particular substance absorbs at a particular wavelength leaving other things alleviating the chances of background contamination/noise.
Protein assay is the determination of concentration or total level of protein in a solution.There are various protein assays employed like bradford assay and lowry assay
No, assay by mass balance and assay by as is basis are not equivalent. Assay by mass balance calculates the amount of a component based on material balance equations, while assay by as is basis measures the amount of a component without accounting for any changes or losses that may occur during processing.
You can't verify assay certificates.
United States Assay Commission was created in 1792.
United States Assay Commission ended in 1980.
The old miners in gold rush country took their nuggets to the local Assay Office, to determine -- to assay -- the value of the metal in their nuggets.
A bandshift assay is a type of assay using gel electrophoresis, in which the mobility of a DNA or RNA probe alone is compared to its mobility in combination with a particular protein.