DNA transfection Mammalian cells Primary cells

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DNA DNA isolation / purification Processed food

DNA DNA isolation / purification Plants Fungus

DNA PCR ORNi-PCR Plasmid DNA

The DNA concentration after using this DNA isolation kit is sometimes too low and thus it is not sufficient for my follow-up experiments. How can I improve it?

Discussions How can I improve my DNA yield?

Get tips on using REPLI-g Mitochondrial DNA Kit (25) to perform Whole Genome Amplification Human

Products Qiagen REPLI-g Mitochondrial DNA Kit (25)

Get tips on using E.Z.N.A.® BAC/PAC DNA-kits to perform Plasmid Isolation Acinetobacter towneri

Products Omega Bio Tek E.Z.N.A.® BAC/PAC DNA-kits

Get tips on using AllPrep DNA/RNA/miRNA Universal Kit to perform RNA isolation / purification Tissue - Mouse Adipose

Products Qiagen AllPrep DNA/RNA/miRNA Universal Kit

Get tips on using AllPrep DNA/RNA/miRNA Universal Kit to perform RNA isolation / purification Tissue - Human Lung

Products Qiagen AllPrep DNA/RNA/miRNA Universal Kit

Get tips on using AllPrep DNA/RNA/Protein Mini Kit to perform Protein isolation Tissue - Human placental tissue

Products Qiagen AllPrep DNA/RNA/Protein Mini Kit

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 MCF-7, MDA-MB-453 human breast cancer

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