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Methyl CpG Binding Protein 2 (Rett Syndrome) (MECP2) ELISA Kits

DNA methylation is the major modification of eukaryotic genomes and plays an essential role in mammalian development.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Mouse MECP2 MECP2 17257 Q9Z2D6
Anti-Rat MECP2 MECP2 29386 Q00566
Anti-Human MECP2 MECP2 4204 P51608
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More ELISA Kits for Methyl CpG Binding Protein 2 (Rett Syndrome) Interaction Partners

Zebrafish Methyl CpG Binding Protein 2 (Rett Syndrome) (MECP2) interaction partners

  1. A mecp2-null allele mutation zebrafish model is developed and the animals are viable and fertile.

Mouse (Murine) Methyl CpG Binding Protein 2 (Rett Syndrome) (MECP2) interaction partners

  1. Cigarette smoke induces proteosomal-mediated degradation of MeCP-2 in embryonic orofacial cells.

  2. Study shows that embryonic primary cortical neurons of Mecp2 null mice display reduced neurite complexity possibly reflecting transcriptional changes that occur long before onset of Rett symptoms.

  3. MeCP2 binding downstream of promoters correlates with increased expression in Mecp2-deficient neurons. Genome-wide association with methylation is in part due to MeCP2's affinity to GC-rich (show RELB ELISA Kits) chromatin.

  4. MeCP2 induced aggregation of heterochromatin that was enhanced in PARP1 (show PARP1 ELISA Kits)-/- cells.

  5. Findings establish miR (show MLXIP ELISA Kits)-199a as a critical downstream target of MeCP2 in RTT pathogenesis by linking MeCP2 with mTOR (show FRAP1 ELISA Kits) signaling.

  6. Results together reveal an important role of MeCP2 SUMOylation in social interaction, memory and synaptic plasticity, and that abnormal MeCP2 SUMOylation is implicated in Rett syndrome.

  7. These results provide new insight into both the fundamental neurobiology of RTT, and potential therapeutic strategies via NF-kappaB (show NFKB1 ELISA Kits) pathway modulation.

  8. Loss of MeCP2 in astrocytes alone is sufficient to result in a dramatic attenuation of the HCVR.

  9. Disturbance of cardiac gene expression and cardiomyocyte structure predisposes Mecp2-null mice to arrhythmias.

  10. a general deficiency of MeCP2 causes an important muscle hypotrophy that is probably the main cause of hypotonia characterizing most Rett syndrome patients.

Human Methyl CpG Binding Protein 2 (Rett Syndrome) (MECP2) interaction partners

  1. The aim of the present study was to evaluate the potential of MeCP2 for use as a therapeutic target for human colorectal cancer.

  2. Functional performance in Rett syndrome patients may relate to the type of Mecp2 mutation

  3. The MECP-2 is the direct targets of miR (show MLXIP ELISA Kits)-370 and miR (show MLXIP ELISA Kits)-373, respectively, in human articular chondrocytes.

  4. revealed a genotype-specific effect of methyl-CpG-binding protein-2 (MeCP2) dysfunction on iPSC-derived neuronal migration and maturation (reduced neurite outgrowth and fewer synapses) in 3D layered hydrogels

  5. Rett Syndrome Mutant Neural Cells Lacks MeCP2 Immunoreactive Bands.

  6. Study suggests that polymorphism in the MECP2 locus is associated with the susceptibility of Iranian patients to systemic lupus erythematosus.

  7. The authors identify NUDT21 (show NUDT21 ELISA Kits) as a novel candidate for intellectual disability and neuropsychiatric disease, and elucidate a mechanism of pathogenesis by MeCP2 dysregulation via altered alternative polyadenylation.

  8. MeCP2 is expressed throughout the gastrointestinal tract (GI). MeCP2 is expressed specifically in the enteric nervous system of the GI.

  9. Study describes the various mutations of MECP2 associated with specific phenotypes and symptoms of Rett syndrome in a large cohort.

  10. MECP2 targets short interspersed nuclear elements, but does not exclude RNA Polymerase III.

Methyl CpG Binding Protein 2 (Rett Syndrome) (MECP2) Antigen Profile

Antigen Summary

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.

Gene names and symbols associated with MECP2

  • methyl CpG binding protein 2 (mecp2) antibody
  • methyl CpG binding protein 2 (Mecp2) antibody
  • methyl CpG binding protein 2 (Rett syndrome) (MECP2) antibody
  • methyl CpG binding protein 2 (Rett syndrome) (mecp2) antibody
  • 1500041B07Rik antibody
  • AUTSX3 antibody
  • BB130002 antibody
  • D630021H01Rik antibody
  • Mbd5 antibody
  • MRX16 antibody
  • MRX79 antibody
  • MRXS13 antibody
  • MRXSL antibody
  • PPMX antibody
  • RS antibody
  • RTS antibody
  • RTT antibody
  • WBP10 antibody
  • wu:fk96a04 antibody
  • zgc:111857 antibody

Protein level used designations for MECP2

methyl-CpG-binding protein 2 , meCp-2 protein , meCP-2 protein , methyl-CpG-binding protein MeCP2

335250 Danio rerio
17257 Mus musculus
29386 Rattus norvegicus
4204 Homo sapiens
612973 Canis lupus familiaris
100328751 Oryctolagus cuniculus
398087 Xenopus laevis
539629 Bos taurus
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