Search results for DNMT3B antibody

Anti-DNMT3B Antibody (R3X23), AntibodySystem, RHJ72201

Anti-DNMT3B Antibody (R3X24), AntibodySystem, RHJ72202

Dnmt3b Antibody (YA4550)(PBS only), MedChemexpress, HY-P84853A

Dnmt3b Antibody (YA4550) is a Mouse-derived and non-conjugated IgG2a monoclonal antibody, targeting to Dnmt3b.

DNA Methyltransferase 3B (DNMT3B) Antibody, Abbexa, abx131181

DNA Methyltransferase 3B Antibody is a Rabbit Polyclonal against DNA Methyltransferase 3B.

Anti-Dnmt3b antibody [EPR26716-583], Abcam, AB321879

Patented technology Our RabMAb ® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb ® patents . What are the advantages of a recombinant monoclonal antibody? This product is a recombinant monoclonal antibody, which offers several advantages including: - High batch-to-batch consistency and reproducibility - Improved sensitivity and specificity - Long-term security of supply - Animal-free batch production For more information, read more on recombinant antibodies .

Anti-Dnmt3b antibody - N-terminal, Abcam, AB227883

DNA Methyltransferase 3 Beta (DNMT3B) Antibody, Abbexa, abx313927

DNMT3B Antibody is a Rabbit Polyclonal against DNMT3B.

DNA Methyltransferase 3 Beta (DNMT3B) Antibody, Abbexa, abx125774

DNMT3B Antibody is a Rabbit Polyclonal against DNMT3B.

DNA Methyltransferase 3 Beta (DNMT3B) Antibody, Abbexa, abx119570

DNMT3B Antibody is a Rabbit Polyclonal antibody against DNMT3B.

DNA Methyltransferase 3 Beta (DNMT3B) Antibody, Abbexa, abx002130

DNMT3B Antibody is a Rabbit Polyclonal antibody against DNMT3B. CpG methylation is an epigenetic modification that is important for embryonic development, imprinting, and X-chromosome inactivation. Studies in mice have demonstrated that DNA methylation is required for mammalian development. This gene encodes a DNA methyltransferase which is thought to function in de novo methylation, rather than maintenance methylation. The protein localizes primarily to the nucleus and its expression is developmentally regulated. Mutations in this gene cause the immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome. Eight alternatively spliced transcript variants have been described. The full length sequences of variants 4 and 5 have not been determined. [provided by RefSeq, May 2011].