PIPA599877
ENOSF1 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA599877-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA599877 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
ENOSF1
Classification
Polyclonal
Conjugate
Unconjugated
Gene
ENOSF1
Gene Alias
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
Host Species
Rabbit
Purification Method
Affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
55556
Content And Storage
-20°C
Form
Liquid
Applications
Western Blot
Concentration
1 mg/mL
Formulation
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4
Gene Accession No.
Q7L5Y1
Gene Symbols
ENOSF1
Immunogen
A synthesized peptide derived from human ENOSF1(Accession Q7L5Y1), corresponding to amino acid residues V388-L438.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
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.