ARG52331

anti-MeCP2 phospho (Ser80) antibody

anti-MeCP2 phospho (Ser80) antibody for Immunohistochemistry,Western blot and Human,Mouse,Rat

Gene Regulation antibody; Neuroscience antibody

Overview

Product Description Rabbit Polyclonal antibody recognizes MeCP2 phospho (Ser80)
Tested Reactivity Hu, Ms, Rat
Tested Application IHC, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name MeCP2
Antigen Species Human
Immunogen Synthetic phospho-peptide corresponding to amino acid residues surrounding Ser80 conjugated to KLH
Conjugation Un-conjugated
Alternate Names MRXSL; RS; MeCp2; Methyl-CpG-binding protein 2; MeCp-2 protein; RTT; AUTSX3; RTS; MRX79; PPMX; MRXS13; MRX16

Application Instructions

Application Suggestion
Tested Application Dilution
IHC1:100
WB1:1000
Application Note Specific for the ~75 kDa MECP2 protein phosphorylated at Ser80 in Western blots of human, Rat and mouse brain extracts. The antibody has also been used successfully for immunohistochemistry on mouse brain sections.
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Serum
Buffer 10 mM HEPES (pH 7.5), 150 mM NaCl, 0.1 mg/ml BSA and 50% Glycerol
Stabilizer 0.1 mg/ml BSA, 50% Glycerol
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 17257 Mouse MECP2

GeneID: 29386 Rat MECP2

GeneID: 4204 Human MECP2

Gene Symbol MECP2
Gene Full Name methyl CpG binding protein 2
Background MECP2 (Methyl-CpG Binding Protein 2) is a chromosomal protein that binds to methylated DNA. It can bind specifically to a single methyl-CpG pair and is not influenced by sequences flanking the methyl-CpGs. MECP2 has been shown to mediate transcriptional repression through interaction with histone deacetylase and the corepressor SIN3A. Defects in MECP2 are the cause of Rett syndrome (RTT). RTT is an X-linked dominant disease, it is a progressive neurologic developmental disorder and one of the most common causes of mental retardation in females. Recent studies have reported a new phosphorylation site at Ser80. Phosphorylation and dephosphorylation of this site may be involved in modulating the dynamic function of MECP2 in neurons transiting between resting and active states within neural circuits that underlie behaviors. (Tao et al., 2009)
Research Area Gene Regulation antibody; Neuroscience antibody
Calculated MW 52 kDa
PTM Phosphorylated on Ser-423 in brain upon synaptic activity, which attenuates its repressor activity and seems to regulate dendritic growth and spine maturation.