|Full Name||methyl CpG binding protein 2 (Rett syndrome)|
|Product Description||Rabbit Polyclonal antibody to MECP2 (methyl CpG binding protein 2 (Rett syndrome))|
|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 some cases of Rett syndrome, a progressive neurologic developmental disorder and one of the most common causes of mental retardation in females. [provided by RefSeq]|
|Synonyms||AUTSX3 antibody, DKFZp686A24160 antibody, MRX16 antibody, MRX79 antibody, MRXS13 antibody, MRXSL antibody, PPMX antibody, RS antibody, RTS antibody, RTT antibody, MECP2 antibody, meCp-2 protein antibody, methyl-CpG-binding protein 2 antibody, methyl CpG binding protein 2 (Rett syndrome) antibody|
|Cellular Localization||Nucleus |
|Immunogen||Recombinant protein encompassing a sequence within the center region of human MECP2. The exact sequence is proprietary.|
|Predicted Cross Reactivity species Predicted cross-reactivity:|
Predicted cross-reactivity is based on sequence homology, with greater than 80% immunogen sequence identity considered positive.
Please note that we are only able to guarantee products to work in applications and species in which they have been tested.
|Human, Mouse, Rat, Rabbit, Rhesus Monkey, Bovine|
|Predict Reactivity Note||Human (100%), Mouse (97%), Rat (97%), Rabbit (94%), Rhesus Monkey (99%), Bovine (98%)|