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methyl CpG binding protein 2 (Rett syndrome), Mouse, Clone: 4B6, Abnova™

Mouse monoclonal antibody raised against a partial recombinant MECP2.

Supplier:  Abnova Corporation H00004204M01

Catalog No. 89-014-149


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Description

Description

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. [provided by RefSeq

Sequence: PKQRRSIIRDRGPMYDDPTLPEGWTRKLKQRKSGRSAGKYDVYLINPQGKAFRSKVELIAYFEKVGDTSLDPNDFDFTVTGRGSPSRREQ
Specifications

Specifications

methyl CpG binding protein 2 (Rett syndrome)
Monoclonal
Unconjugated
PBS with no preservative; pH 7.4
BC011612
MECP2
MECP2 (AAH11612, 81 a.a. ∼ 170 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
100 μg
Transcription Regulation
4204
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
IgG2a κ
ELISA, Immunohistochemistry (PFA fixed), Western Blot
4B6
Mouse monoclonal antibody raised against a partial recombinant MECP2.
MECP2
AUTSX3/DKFZp686A24160/MRX16/MRX79/MRXS13/MRXSL/PPMX/RTS/RTT
Mouse
Affinity Purified
RUO
Primary
Human, Mouse
Antibody
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