DNMT3A Polyclonal Antibody


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Cat.No.:  EAb-0526
Product Name:  DNMT3A Polyclonal Antibody
Antibody Type:  Polyclonal
Immunogen:  This antibody was developed against synthetic peptides corresponding to areas around amino acids 125-175 and another around 175-225 of Dnmt3a.
Host:  Rabbit
Isotype:  IgG
Antibody Target:  DNMT3A
Purification:  Protein G purified
Appearance:  Liquid
Formulation:  0.2 ml PBS and 0.05% BSA
Applications:  WB
Recommended Dilutions/Conditions:  Western Blot 3 - 5ug/ml
Recommended dilutions/conditions may not be available for all applications. Specific conditions for reactivity should be optimized by the end user.
Species Reactivity:  Human
Storage:  -20°C
Storage Buffer:  0.05% Sodium Azide
Warning:  For Research Use Only! Not For Use in Humans.
Alternative Name:  DNA (cytosine-5-)-methyltransferase 3 alpha; DNA (cytosine-5)-methyltransferase 3A; DNA cytosine methyltransferase 3A2; DNA methyltransferase HsaIIIA; DNA MTase HsaIIIA; DNMT3A; DNMT3A2; EC 2.1.1.37; M.HsaIIIA
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, 3 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 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 occurs in patients with a rare autosomal recessive disorder, termed ICF (immunodeficiency, centromeric instability, and facial anomalies) syndrome.

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

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