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|Tested species reactivity||Human, Mouse, Pig, Rat, Zebrafish|
|Published species reactivity||Not Applicable|
|Host / Isotype||Mouse / IgG1, kappa|
|Immunogen||Synthetic peptide corresponding to amino acids 637-650 (EKDDREDKENAFKR) of human Dnmt1.|
|Contains||0.05% sodium azide|
|Storage Conditions||Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.|
|Tested Applications||Dilution *|
|ChIP assay (ChIP)||1:10-1:500|
|Immunohistochemistry (Frozen) (IHC (F))||1:1000|
|Immunohistochemistry - Free Floating (IHC (Free))||1:1000|
|Immunohistochemistry (Paraffin) (IHC (P))||1-2 µg/ml|
|Western Blot (WB)||0.1-0.5 µg/ml|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
|Western Blot (WB)||See 1 publications below|
Suggested positive control: human kidney (IHC), mouse ES cells (WB).
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. Dnmt1 co-purifies with the retinoblastoma (Rb) tumour suppressor gene product, E2F1, and HDAC1. Dnmt1 also cooperates with Rb to repress transcription from promoters containing E2F-binding sites suggesting a link between DNA methylation, histone deacetylase and sequence-specific DNA binding activity, as well as a growth-regulatory pathway that is disrupted in nearly all cancer cells.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
DNMT1 and HDAC2 Cooperate to Facilitate Aberrant Promoter Methylation in Inorganic Phosphate-Induced Endothelial-Mesenchymal Transition.
MA5-16169 was used in western blot to study the interaction between DNMT1 and HDAC2 and how they cooperate to facilitate aberrant promoter methylation in inorganic phosphate-induced endothelial-mesenchymal transition
|Tan X,Xu X,Zeisberg M,Zeisberg EM||PloS one (11:null)||2016|
CXXC finger protein 9; CXXC-type zinc finger protein 9; CXXC9; ddn; DNA (cytosine-5)-methyltransferase 1; DNA methyltransferase 1; DNA methyltransferase HsaI; DNA methyltransferase MmuI; DNA MTase HsaI; DNA MTase MmuI; DNMT; Dnmt1; HSN1E; m.HsaI; MCMT
ADCADN; AIM; cb1075; cb983; CXXC9; dmnt1; DNMT; DNMT1; Dnmt1o; fb05h01; HSN1E; m.HsaI; m.MmuI; MCMT; Met-1; Met1; MommeD2; mta; MTase; Uim; wu:fb05h01