DNA Methyltransferase 3a Monoclonal Antibody (Clone 64B814.1)


  • Specification
  • Target Information
  • Related Products
Cat.No.:  EAb-0287
Product Name:  DNA Methyltransferase 3a Monoclonal Antibody (Clone 64B814.1)
Product Overview:  Monoclonal antibody to detect DNMT3a in Human and Mouse samples
Antibody Type:  Monoclonal
Clone Designation:  64B814.1
Immunogen:  Recombinant mouse His-tagged DNMT3a expressed in bacteria
Host:  Mouse
Isotype:  IgG1κ
Antibody Target:  DNMT3A
Purification:  Protein G purified
Appearance:  Liquid
Formulation:  100 µg protein G-purified IgG in 200 µl PBS containing 0.05% BSA and 0.05% sodium azide
Applications:  Western blot, Immunofluorescence, Immunocytochemistry
Recommended Dilutions/Conditions:  Western blot: 1-3 µg/ml, IF/ICC: 5 µg/ml.
Recommended dilutions/conditions may not be available for all applications. Specific conditions for reactivity should be optimized by the end user.
Positive Control:  Western blot: Transfected 293 cell lysate, untransfected 293 cell lysate
Species Reactivity:  Human, mouse
Shipping:  Wet ice
Storage:  -20°C
Warning:  For Research Use Only! Not For Use in Humans.
Accession:  O88508
Alternative Name:  DNMT3a
Scientific Background:  Methylation of DNA at cytosine residues plays an important role in regulation of gene expression, genomic imprinting, and is essential for mammalian development. Hypermethylation of CpG islands in tumor suppressor genes or hypomethylation of bulk genomic DNA may be linked with development of cancer. To date, three families of mammalian DNA methyltransferase genes have been identified which include DNMT1, DNMT2, and DNMT3. DNMT1 is constitutively expressed in proliferating cells and inactivation of this gene causes global demethylation of genomic DNA and embryonic lethality. DNMT2 is expressed at low levels in adult tissues and its inactivation does not affect DNA methylation or maintenance of methylation. The DNMT3 family members, DNMT3a and DNMT3b, are strongly expressed in embryonic stem (ES) cells but their expression is down regulated in differentiating ES cells and is low in adult somatic tissue. Recently, it has been shown that naturally occurring mutations of DNMT3b gene occur in patients with a rare autosomal recessive disorder, termed ICF (immunodeficiency, centromeric instability, and facial anomalies) syndrome.

Online Inquiry

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

USA

Enter your email here to subscribe.

Follow us on

Easy access to products and services you need from our library via powerful searching tools

Copyright © Creative BioMart. All Rights Reserved.