MECP2 antibody

Synonyms:AUTSX3 antibody
Catalogue No.:FNab05082Reactivity:Human, Mouse
Host:RabbitTested Application:ELISA, IHC, WB
Clonality:polyclonalIsotype:IgG
  • SPECIFICATIONS
Product Name
MECP2 antibody
Catalogue No.
FNab05082
Size
100μg
Form
liquid
Purification
Immunogen affinity purified
Purity
≥95% as determined by SDS-PAGE
Clonality
polyclonal
Isotype
IgG
Storage
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.)
Immunogen
Immunogen
methyl CpG binding protein 2 (Rett syndrome)
Alternative Names
AUTSX3 antibody
UniProt ID
P51608
Observed MW
83 kDa
Application
Tested Applications
ELISA, IHC, WB
Recommended dilution
WB: 1:500 - 1:1000; IHC: 1:50 - 1:100
Validated Images
MDA-MB-453s cells were subjected to SDS PAGE followed by western blot with FNab05082(MECP2 Antibody) at dilution of 1:1000
Immunohistochemistry of paraffin-embedded human gastric cancer using FNab05082(MECP2 antibody) at dilution of 1:50
Background
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 isoforms.