
Thermo Fisher Scientific MeCP2 Polyclonal Antibody
Human MeCP2 단백질을 인식하는 토끼 폴리클로날 항체로, Western blot, IHC, ELISA 등에 사용 가능. 고순도 친화 크로마토그래피 정제. -20°C에서 안정적 보관 가능하며 MeCP2 관련 연구에 적합.
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Applications
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:1,000 |
| Immunohistochemistry (IHC) | 1:200 |
| ELISA | 1:10,000–1:15,000 |
Product Specifications
| Specification | Description |
|---|---|
| Species Reactivity | Chicken, Human |
| Host/Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Anti-MeCP2 antibody prepared from whole rabbit serum immunized with a synthetic peptide corresponding to the C-terminal portion of human MeCP2 conjugated to Keyhole Limpet Hemocyanin (KLH). |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Affinity chromatography |
| Storage buffer | 0.02M potassium phosphate, pH 7.2, with 0.15M NaCl |
| Contains | 0.01% sodium azide |
| Storage conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping conditions | Ambient (domestic); Wet ice (international) |
Product Specific Information
Store vial at -20°C prior to opening. Aliquot contents and freeze at -20°C or below for extended storage. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature.
This product is stable for several weeks at 4°C as an undiluted liquid. Dilute only prior to immediate use.
This affinity-purified antibody is directed against human MeCP2. A BLAST analysis suggests cross-reactivity with mouse, rat, and Macaca fascicularis based on 100% sequence homology.
Target Information
MECP2 belongs to a family of nuclear proteins (including MBD1, MBD2, MBD3, and MBD4) that contain a methyl-CpG binding domain. MECP2 binds specifically to methylated DNA, playing a key role in mammalian development and transcriptional repression of methylated gene promoters.
Unlike other MBD family members, MECP2 is X-linked and subject to X inactivation. It is dispensable in stem cells but essential for embryonic development. Mutations in the MECP2 gene cause most cases of Rett syndrome, a progressive neurological developmental disorder and a major cause of mental retardation in females.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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