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ENOSF1 Rabbit anti-Human, Polyclonal, Bioss
SDP

Rabbit Polyclonal Antibody

Supplier:  Bioss BS13070R

Encompass_Preferred

Catalog No. 50-198-2593


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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.
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
Protein A
RUO
55556
-20°C
Liquid
Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot
1 μg/mL
PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH
Q7L5Y1
ENOSF1
KLH conjugated synthetic peptide derived from human ENOSF1.
100 μL
Primary
Human
Antibody
IgG
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