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Western blot of neonatal rat brain showing specific immunolabeling of the ~75k MeCP2 protein phosphorylated at Ser 80 using MeCP2 (phospho Ser80) antibody (GTX82658).
Western blot of neonatal rat brain showing specific immunolabeling of the ~75k MeCP2 protein phosphorylated at Ser 80 using MeCP2 (phospho Ser80) antibody (GTX82658).
Western blot of neonatal rat brain showing specific immunolabeling of the ~75k MeCP2 protein phosphorylated at Ser 80 using MeCP2 (phospho Ser80) antibody (GTX82658).

MECP2 (phospho Ser80) antibody

GTX82658
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetMECP2
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Overview

  • Supplier
    GeneTex
  • Product Name
    MECP2 (phospho Ser80) antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    Optimal working dilutions should be determined experimentally by the end user.
  • Applications
    Western Blot, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID4204
  • Target name
    MECP2
  • Target description
    methyl-CpG binding protein 2
  • Target synonyms
    AUTSX3; meCp-2 protein; methyl-CpG-binding protein 2; MRX16; MRX79; MRXS13; MRXSL; PPMX; RS; RTS; RTT
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP51608
  • Protein Name
    Methyl-CpG-binding protein 2
  • Scientific 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 cognitive disability in females. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2015]
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Association of CaMK2A and MeCP2 signaling pathways with cognitive ability in adolescents. Lee LC et al., 2021 Oct 4, Mol Brain
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