Immunofluorscence  53BP1 [H-300] Rabbit Human

Get tips on using DMEM HIGH GLUCOSE to perform Mammalian cell culture media HFLS-OA

Get tips on using SPLInsert™ Hanging to perform Cell migration / Invasion cell type - HaCat

Get tips on using pBud-hIL-7 to perform Protein Expression Eukaryotic cells - CHO hIL-7

Get tips on using HIF-1 alpha Antibody to perform Western blotting HIF-1 alpha

Get tips on using HSP60 monoclonal antibody (LK-1) to perform Western blotting Hsp60

Get tips on using HDAC1 Antibody (10E2): sc-81598 to perform Western blotting HDAC1

Get tips on using ErbB2 (HER-2) Antibody Cocktail to perform Western blotting HER2

Get tips on using jetPEI®-HUVEC to perform DNA transfection Mammalian cells - Primary cells HUVEC

Get tips on using HuR siRNA to perform siRNA / miRNA gene silencing Rat - IEC-6 HuR Lipid

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.