MeCP2 rabbit pAb

MeCP2 rabbit pAb

• Description: DNA methylation is the major modification of eukaryotic genomes and plays an essential role in mammalian development. Human proteins MECP2, MBD1, MBD2, MBD3, and MBD4 comprise a family of nuclear proteins related by the presence in each of a methyl-CpG binding domain (MBD). Each of these proteins, with the exception of MBD3, is capable of binding specifically to methylated DNA. MECP2, MBD1 and MBD2 can also repress transcription from methylated gene promoters. In contrast to other MBD family members, MECP2 is X-linked and subject to X inactivation. MECP2 is dispensible in stem cells, but is essential for embryonic development. MECP2 gene mutations are the cause of most cases of Rett syndrome, a progressive neurologic developmental disorder and one of the most common causes of mental retardation in females. Alternative splicing results in multiple transcript variants encoding different isofor
• Synonyms: Methyl-CpG-binding protein 2 (MeCp-2 protein) (MeCp2)
• Gene ID: 4204
• UniProt: P51608
• Cellular Locus: Nucleus. Colocalized with methyl-CpG in the genome. Colocalized with TBL1X to the heterochromatin foci..
• Host: Rabbit
• Species Reactivity: Human
• Immunogen: Synthetic Peptide of MeCP2 AA range: 313-363
• Clonality: Polyclonal
• Validated Applications: WB
• Stability: 1 year
• Dilution: WB: 1:2000
• Molecular Weight: 53kD
• Storage Conditions: PBS with 0.02% sodium azide and 50% glycerol pH 7.4. Store at -20°C. Avoid repeated freeze-thaw cycles.