Site Directed Mutagenesis (SDM) Human Insertion IMR-32

Get tips on using Smad1 Antibody (A-4): sc-7965 to perform Western blotting Smad1

Get tips on using Recombinant Anti-Smad4 antibody [EP618Y] (ab40759) to perform Western blotting Smad4

Get tips on using Smad4 Antibody (B-8): sc-7966 to perform Western blotting Smad4

Get tips on using Smad2 Antibody (YZ-13): sc-101153 to perform Western blotting Smad2

Get tips on using Anti-Smad2 (phospho S467) antibody (ab53100) to perform Western blotting Smad2

Get tips on using Phospho-SMAD2 (Ser465, Ser467) Monoclonal Antibody (H.205.4) to perform Western blotting Smad2

Get tips on using Recombinant Anti-alpha smooth muscle Actin antibody [E184] (ab32575) to perform Western blotting Smooth muscle actin

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.

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.