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Thermo Fisher Scientific Phospho-MECP2 (Ser421) Polyclonal Antibody
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Thermo Fisher Scientific Phospho-MECP2 (Ser421) Polyclonal Antibody

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Phospho-MECP2 (Ser421) 항체로 인간, 생쥐, 랫드 시료에서 인산화된 MeCP2 단백질 검출에 적합. Western blot 및 면역세포염색(ICC/IF)에 사용 가능. 고순도 항원 친화 크로마토그래피 정제. PBS/BSA/글리세롤 완충액에 보관.

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마지막 업데이트 2025. 08. 02. 오전 09:41
Thermo Fisher Scientific PA5143717 Phospho-MECP2 (Ser421) Polyclonal Antibody 100 ul pk판매 단위 pk ·
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786,900원VAT 포함 865,590원

Thermo Fisher Scientific · Thermo Fisher Scientific Phospho-MECP2 (Ser421) Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500
Immunocytochemistry (ICC/IF) 1:250

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen phospho-MeCP2 (Ser-421) synthetic peptide (coupled to KLH) corresponding to amino acid residues surrounding serine 421 in mouse MeCP2. This peptide sequence is highly conserved in rat and human MeCP2, and has low homology to other nuclear proteins.
Conjugate Unconjugated
Form Liquid
Concentration 1.0 mg/mL
Purification Antigen affinity chromatography
Storage buffer PBS with 1 mg/mL BSA, 50% glycerol
Contains 0.05% sodium azide
Storage conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping conditions Wet ice
RRID AB_2942945

Product Specific Information

This antibody detects a 75 kDa protein corresponding to the molecular mass of MeCP2 on SDS-PAGE immunoblots of human PC3 cells treated with calyculin A and in mouse brain tissue. These reactivities are not observed after lambda phosphatase treatment.

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, a key modification in eukaryotic genomes crucial for mammalian development. It represses transcription from methylated gene promoters and, unlike other MBD family members, is X-linked and subject to X inactivation. MECP2 is dispensable in stem cells but essential for embryonic development. Mutations in the MECP2 gene are the primary cause of Rett syndrome, a progressive neurological developmental disorder and one of the most common causes of intellectual disability in females.


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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