Product Overview
HeLa cell lines were engineered into double-knockout lines by CRISPR technology. The double knockout genotype was verified by PCR followed by sequencing. The DNMT3B knockout cell lysate are the cell homogenate in RIPA buffer made from the KO cell lines. A vial of lysate from the parental cell line was also provided as an internal control.
Alternative Names
DNMT3B; DNA methyltransferase 3B; DNA (cytosine-5)-methyltransferase 3B; m.MmuIIIB; DNA MTase MmuIIIB; DNA methyltransferase MmuIIIB; MGC124407;
Application Notes
Prior to SDS-PAGE fractionation, boil the lysate for 5 minutes.
Dilution
Lysate samples can be diluted with 2x SDS Sample Buffer.
After dilution, the protein sample should be aliquoted and stored at -20°C for long term storage.
Concentration
The protein concentration was determined with BCA assay.
Storage
Store at -20°C. Avoid repeated freeze-thaw cycles.
Citations
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Peters, DD; Lepikhov, K; et al. Effect of IVF and laser zona dissection on DNA methylation pattern of mouse zygotes. MAMMALIAN GENOME 20:664-673(2009).
Coppede, F; Ricciardi, R; et al. Association of the DNMT3B-579G > T Polymorphism with Risk of Thymomas in Patients with Myasthenia Gravis. PLOS ONE 8:-(2013).