MBD5

gene product
FLJ11113, KIAA1461
This gene encodes a member of the methyl-CpG-binding domain (MBD) family. The MBD consists of about 70 residues and is the minimal region required for a methyl-CpG-binding protein binding specifically to methylated DNA. In addition to the MBD domain, this protein contains a PWWP domain (Pro-Trp-Trp-Pro motif), which consists of 100-150 amino acids and is found in numerous proteins that are involved in cell division, growth and differentiation. Mutations in this gene cause mental retardation autosomal dominant type 1. Haploinsufficiency of this gene is associated with a syndrome involving microcephaly, intellectual disabilities, severe speech impairment, and seizures. Alternatively spliced transcript variants have been found, but their full-length nature is not determined. [provided by RefSeq, Mar 2010]
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102 antibodies from 17 providers.

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AntibodyRefsTypeWBELICCIPIHCFC
Novus Biologicals
3 antibodies
Abnova Corporation
4 antibodies
antibodies-online
29 antibodies
Biorbyt
6 antibodies
NovoPro Bioscience Inc.
1 antibody
Proteintech Group
1 antibody
Atlas Antibodies
1 antibody
GeneTex
1 antibody
Invitrogen Antibodies
1 antibody
Abiocode, Inc.
2 antibodies
LifeSpan BioSciences, Inc.
31 antibodies
Creative Diagnostics
2 antibodies
MyBioSource
2 antibodies
Creative Biolabs
1 antibody
United States Biological
12 antibodies
Abbexa
3 antibodies
Sigma-Aldrich
2 antibodies