What are the potential sources of error in Bradford’s assay and LDH activity test?
Sources of error in Bradford assay
The absorbance of the protein sample is lower than expected
The absorbance of the protein sample is higher than expected
The absorbance of the standard is lower than expected
Samples are dark blue
Detergents in your protein buffer:
Dialyze your protein sample or dilute the sample to reduce the level of detergents.
Sources of error in LDH activity
Hemolysis RBCs found in serum(contain 100-150 times )
Analyte stability
Run assay asap or store at room temperature
Prolonged contact of serum and cells
use of poor quality of reagents e.g NADH & NAD+, homeolysed sample
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