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Invitrogen™ ENOSF1 Polyclonal Antibody

Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA599877

Catalog No. PIPA599877


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Description

Description

Antibody detects endogenous levels of total ENOSF1.

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.
TRUSTED_SUSTAINABILITY
Specifications

Specifications

ENOSF1
Polyclonal
Unconjugated
ENOSF1
antisense RNA to thymidylate synthase; enolase superfamily member 1; ENOSF1; HSRTSBETA; L-fuconate dehydratase; mitochondrial enolase superfamily member 1; rTS; rTS alpha; rTS beta; TYMSAS
Rabbit
Affinity chromatography
RUO
55556
-20°C
Liquid
Western Blot
1 mg/mL
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4
Q7L5Y1
ENOSF1
A synthesized peptide derived from human ENOSF1(Accession Q7L5Y1), corresponding to amino acid residues V388-L438.
100 μL
Primary
Human
Antibody
IgG
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