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anti-Methyl CpG Binding Protein 2 (Rett Syndrome) (MECP2) Antibodies

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

list all antibodies 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 Antibodies against 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. 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 Antibodies) chromatin.

  2. MeCP2 induced aggregation of heterochromatin that was enhanced in PARP1 (show PARP1 Antibodies)-/- cells.

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

  4. 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.

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

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

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

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

  9. The data of this study demonstrated a role for MeCP2 in growth and maturation of newborn granule cells in developing fetal and adult hippocampus

  10. These results demonstrate a novel role for miR (show MLXIP Antibodies)-15a in neuronal development and provide a missing link in the regulation of BDNF (show BDNF Antibodies) by MeCP2.

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

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

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

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

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

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

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

  7. MECP2, a gene associated with Rett syndrome in humans, shows conserved coding regions, independent Alu insertions, and a novel transcript across primate evolution

  8. Results show that these antibodies are highly specific for dense fine speckles 70 (show PSIP1 Antibodies) protein DFS70 (show PSIP1 Antibodies)/LEDGFp75 and do not target methyl CpG binding protein 2 (MeCP2).

  9. this study describes somatic, neurologic and mental symptoms of the patients with X chromosome distal long arm microduplications encompassing the MECP2 gene.

  10. Effects of the most common Rett Syndrome -causing mutations on the stability of methyl-CpG-binding domain of MeCP2 have been investigated through in silico and in vitro studies.

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

Protein 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

GENE ID SPECIES
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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