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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) 폴리클로날 항체로, Western blot, IHC, ICC/IF에 사용 가능. Mouse와 Rat에 반응하며, Rabbit IgG 유래. 친화 크로마토그래피로 정제되었으며, -20°C에서 보관. 인간 및 영장류에도 반응 예측됨.

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마지막 업데이트 2025. 08. 02. 오후 07:55
Thermo Fisher Scientific PA535396 Phospho-MECP2 (Ser421) Polyclonal Antibody 100 ul pk판매 단위 pk ·
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699,000원VAT 포함 768,900원

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

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1:1,000 View 2 publications
Immunohistochemistry (IHC) - View 1 publication
Immunocytochemistry (ICC/IF) - View 1 publication

Product Specifications

항목 내용
Species Reactivity Mouse, Rat
Published Species Not Applicable
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic phospho-peptide corresponding to amino acid residues surrounding Ser421 of mouse MeCP2 conjugated to KLH
Conjugate Unconjugated
Form Liquid
Concentration ~0.25 mg/mL
Purification Affinity chromatography
Storage Buffer 0.01M HEPES, pH 7.5, with 0.1 mg/mL BSA, 50% glycerol, 0.15M NaCl
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2552706

Product Specific Information

  • This antibody is predicted to react with human and non-human primate based on 100% sequence homology.
  • Contains enough material to conduct approximately 10 mini-Western blots.

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 essential for mammalian development. It can repress transcription from 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 are the primary cause of Rett syndrome, a progressive neurological developmental disorder and a common 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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