Comparison

Anti-MeCP2 (Ser421) Antibody

Item no. ABC-AN1445
Manufacturer Abcepta
Amount 100 ul
Category
Specific against other
Host Rabbit
Isotype IgG
Alias AUTSX 3 antibody,AUTSX3 antibody,DKFZp686A24160 antibody,Mbd 5 antibody,Mbd5 antibody,MECP 2 antibody,MeCP 2 protein antibody,MeCP-2 protein antibody,Mecp2 antibody,MECP2_HUMAN antibody,Methyl CpG binding protein 2 (Rett syndrome) antibody,Methyl CpG binding protein 2 antibody,Methyl-CpG-binding protein 2 antibody,MRX 16 antibody,MRX 79 antibody,MRX16 antibody,MRX79 antibody,MRXS 13 antibody,MRXS13 antibody,MRXSL antibody,PPMX antibody,RS antibody,RTS antibody,RTT antibody,WBP 10 antibody,WBP10 antibody
Available
Manufacturer - Category
Primary Antibodies; Neuroscience
Manufacturer - Targets
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 (Nan et al., 1998). Defects in MeCP2 are the cause of Rett syndrome (RTT) (Amir et al., 1999). 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 Ser-421. Phosphorylation and dephosphorylation of this site may be involved in regulation of behavioral responses to chronic antidepressant treatment (Hutchinson et al., 2012).
Bio 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 (Nan et al., 1998). Defects in MeCP2 are the cause of Rett syndrome (RTT) (Amir et al., 1999). 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 Ser-421. Phosphorylation and dephosphorylation of this site may be involved in regulation of behavioral responses to chronic antidepressant treatment (Hutchinson et al., 2012).
Clonality
Polyclonal
Gene Name
Mecp2
Subtitle
Our Anti-MeCP2 (Ser421) rabbit polyclonal phosphospecific primary antibody from PhosphoSolutions is
Calculated Molecular Weight
52307
Formulation
Antigen Affinity Purified from Pooled Serum

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 100 ul
Available: In stock
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