siRNA / RNAi /miRNA transfection Human Cells THP-1

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Get tips on using Anti-TATA binding protein TBP antibody [58C9] - Loading Control (ab61411) to perform Western blotting TBP

Products Abcam Anti-TATA binding protein TBP antibody [58C9] - Loading Control (ab61411)

Get tips on using Monoclonal Anti-Collagen, Type III antibody produced in mouse to perform Western blotting Type III collagen

Products Sigma-Aldrich Monoclonal Anti-Collagen, Type III antibody produced in mouse

Get tips on using TopTaq Master Mix Kit to perform PCR Conventional / Qualitative PCR - mammalian DNA

Products Qiagen TopTaq Master Mix Kit

Get tips on using QIAexpress Type IV Kit to perform Protein tag Purification of His-tagged proteins

Products Qiagen QIAexpress Type IV Kit

Does anyone know how “strong” the PCR product of methylation specific PCR is? I kept my PCR products at 4C for about 3 weeks and then at room temperature for another week. Will I be able to use them for sequencing?

Discussions How “strong” is the PCR product of methylation specific PCR?

Get tips on using Type-it HRM PCR Kit (2000) to perform High-resolution melting (HRM) analysis Bacterial

Products Qiagen Type-it HRM PCR Kit (2000)

Get tips on using Anti-Collagen Type II Antibody, clone 6B3 to perform Immunohistochemistry Mouse - Col II

Products Merck Millipore Anti-Collagen Type II Antibody, clone 6B3

DNA Whole Genome Amplification Cell lines

The estimation of DNA methylation level heavily depends on the complete conversion of non-methylated DNA cytosines. It is crucial to ensure complete conversion of non-methylated cytosines in DNA. Therefore, it is important to incorporate controls for bisulfite reactions, as well as to pay attention to the appearance of cytosines in non-CpG sites after sequencing, which is an indicator of incomplete conversion.

DNA DNA methylation profiling Whole genome profiling rat liver tissue

The estimation of DNA methylation level heavily depends on the complete conversion of non-methylated DNA cytosines. It is crucial to ensure complete conversion of non-methylated cytosines in DNA. Therefore, it is important to incorporate controls for bisulfite reactions, as well as to pay attention to the appearance of cytosines in non-CpG sites after sequencing, which is an indicator of incomplete conversion.

DNA DNA methylation profiling Whole genome profiling rat mammary tissue

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