Get tips on using RNeasy Plus Universal Kits to perform RNA isolation / purification Tissue - Mouse Thymus
Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - Mouse Muscle
Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - Mouse Liver
Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - Mouse Kidney
Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - Mouse Brain
Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - Mouse Bone
Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - Mouse Lung
Get tips on using NucleoSpin® miRNA to perform RNA isolation / purification Tissue - Mouse Brain
Get tips on using TriPure Isolation Reagent to perform RNA isolation / purification Tissue - rat pancreas tissue
DNA microarrays enable researchers to monitor the expression of thousands of genes simultaneously. However, the sensitivity, accuracy, specificity, and reproducibility are major challenges for this technology. Cross-hybridization, combination with splice variants, is a prime source for the discrepancies in differential gene expression calls among various microarray platforms. Removing (either from production or downstream bioinformatic analysis) and/or redesigning the microarray probes prone to cross-hybridization is a reasonable strategy to increase the hybridization specificity and hence, the accuracy of the microarray measurements.
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