MECP2 Polyclonal Antibody, Invitrogen™
Manufacturer: Invitrogen
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | 50-255-0797-Each-of-1 | In Stock | ₹ 40,050.00 |
50-255-0797 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 40,050.00
GST (18%): ₹ 7,209.00
Total Price: ₹ 47,259.00
Antigen
MECP2
Classification
Polyclonal
Conjugate
Unconjugated
Gene
Mecp2
Gene Alias
1500041B07Rik, AUTSX3, D630021H01Rik, DKFZp686A24160, Mbd5, MECP2, MeCp-2 protein, methyl CpG binding protein 2, methyl-CpG binding protein 2, methyl-CpG-binding protein 2, MRX16, MRX79, MRXS13, MRXSL, PPMX, RS, RTS, RTT, testis tissue sperm-binding protein Li 41a, WBP10
Host Species
Rabbit
Purification Method
Affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
4204
Content And Storage
-20°, C, Avoid Freeze/Thaw Cycles
Isotype
IgG
Applications
ChIP Assay, ELISA, Immunoprecipitation, Immunoprecipitation, Western Blot
Concentration
Conc. Not Determined
Formulation
PBS with 0.05% ProClin 300, 0.05% sodium azide
Gene Accession No.
P51608
Gene Symbols
Mecp2
Immunogen
Raised against the C-term of human MECP2.
Quantity
50 μg
Primary or Secondary
Primary
Target Species
Human
Form
Liquid
Related Products
Description
- MECP2 belongs to a family of nuclear proteins (including MBD1, MBD2, MBD3 and MBD4) that have a methyl-CpG binding domain
- MECP2 is capable of binding specifically to methylated DNA
- DNA methylation is the major modification of eukaryotic genomes and plays an essential role in mammalian development
- MECP2 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.