Mouse Monoclonal 5-Methylcytosine antibody - conjugated to Biotin. Suitable for ICC/IF and reacts with Chemical samples. Cited in 1 publication. Immunogen corresponding to Chemical / Small Molecule corresponding to 5-Methylcytosine.
IgM
Mouse
Biotin
pH: 6 - 8.5
Constituents: 50% Glycerol (glycerin, glycerine), 50% PBS
Liquid
Monoclonal
ICC/IF | |
---|---|
Chemical | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Chemical | Dilution info 1/50.00000 - 1/100.00000 | Notes - |
Select an associated product type
5 Methycytosine, 5-Me Cytidine, 5-Me Cytosine, 5-Methyl-Cytidine, 5-Methyl-Cytosine, 5-MethylCytidine, 5-MethylCytosine, 5-mC, 5-meC, methyl CpG
Mouse Monoclonal 5-Methylcytosine antibody - conjugated to Biotin. Suitable for ICC/IF and reacts with Chemical samples. Cited in 1 publication. Immunogen corresponding to Chemical / Small Molecule corresponding to 5-Methylcytosine.
5 Methycytosine, 5-Me Cytidine, 5-Me Cytosine, 5-Methyl-Cytidine, 5-Methyl-Cytosine, 5-MethylCytidine, 5-MethylCytosine, 5-mC, 5-meC, methyl CpG
IgM
Mouse
Biotin
pH: 6 - 8.5
Constituents: 50% Glycerol (glycerin, glycerine), 50% PBS
Liquid
Monoclonal
5MC-CD
IgM fraction
Blue Ice
1-2 weeks
+4°C
-20°C
Upon delivery aliquot
Avoid freeze / thaw cycle
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5-methylcytosine often referred to as 5-mC 5-methyl cytosine or 5-methylcytidine is a methylated form of the nucleobase cytosine found in the DNA of various organisms. This modification typically occurs at the carbon 5 position of the cytosine ring contributing to the epigenetic regulation of gene expression. While the mass of 5-mC itself is relatively small since it is a modified nucleotide its impact on gene regulation is significant. 5-mC is widely expressed in the genome of higher eukaryotes particularly in CpG dinucleotides where it plays a role in mammalian development and cell differentiation.
Cytosine methylation affects DNA-protein interactions leading to changes in chromatin structure and the regulation of gene activity. 5-methylcytosine is an important player in the chromatin modification complex where it collaborates with other epigenetic marks to control gene expression profiles. This modified nucleotide helps to stabilize gene silencing maintaining the closed chromatin state which inhibits the transcription machinery's access to specific genomic regions. Such silencing is vital during processes like X-chromosome inactivation and imprinting.
Researchers have identified 5-mC within two critical pathways: DNA methylation and demethylation cycle and histone modification pathway. In the DNA methylation pathway 5-mC interacts closely with proteins like DNA methyltransferases (DNMTs) which directly add methyl groups to cytosine bases. In the context of histone modification 5-mC influences the binding of methyl-CpG-binding domain (MBD) proteins which read and interpret methylated DNA marks affecting histone modification and DNA accessibility.
The dysregulation of 5-methylcytosine patterns associates prominently with cancer and neurological disorders. Abnormal methylation patterns where 5-mC is either hypermethylated or hypomethylated can lead to the silencing of tumor suppressor genes or activation of oncogenes forming a basis for cancer development. In neurological disorders altered 5-mC levels link to conditions such as Rett syndrome where the dysfunction of the associated protein MeCP2 an important reader of 5-mC contributes to the disease pathology.
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This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
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Immunofluorescence analysis of Clamydomonas me-1 cells, labeling 5-Methyl Cytosine using ab179914 at a 1/50 dilution, followed by FITC-conjugated secondary antibody (green). DAPI was used to stain DNA (magenta). Upper panels (a, b and c) correspond to vegetative cells and lower panels (d, e and f) to gametes.
Immunofluorescence analysis of mouse embryonic cells, labeling 5-Methyl Cytosine using ab179914 at a 1/50 dilution. DAPI was used to stain DNA (magenta).
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