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This work demonstrates a new immobilisation platform for the development of a sensitive and label-less impedimetric and piezoelectric immunosensor.
The sequence data obtained was used for the development of a sensitive PCR which is entirely specific for H. hammondi and incorporates an internal control.
For therapeutic monitoring and pharmacokinetic studies of lenalidomide (LND), the potent drug for treatment of multiple myeloma (MM), a specific antibody was required for the development of a sensitive immunoassay system for the accurate determination of LND in plasma.
This enabled the use of specific limits for any variation of variables amongst those tested to be set up, resulting in the apparatus necessary for the development of a sensitive continuous control system.
Importanly, the layered QDs with highly intense ECL could provide a promising candidate for the development of a sensitive ECL biosensor, and it is for the first time that layered QDs were used as ECL probe and combined with recycling amplification for highly sensitive detection of biomolecules.
This provides a rationale for the development of a sensitive assay that can detect tat/ rev msRNA upon maximal stimulation.
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The development of a sensitive analytical method for the determination of perchlorate is therefore of the highest interest or public health.
We herefore report the formation and application of the Prussian blue complex in the development of a sensitive spectrophotometric method for the determination of ETD.
Here we describe the development of a sensitive single step RT-PCR assay for the detection of KFD viral RNA.
There is an unmet need for the development of a rapid, sensitive test for the identification of viruses and classification of viral strains.
Thus, this gene is probably the best target for the development of a highly sensitive detection method.
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