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Key Documents

07-013

Sigma-Aldrich

Anti-MeCP2 Antibody

Upstate®, from rabbit

Sinónimos:

MeCP-2 protein, mental retardation, X-linked 16, mental retardation, X-linked 79, methyl CpG binding protein 2, methyl CpG binding protein 2 (Rett syndrome)

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About This Item

Código UNSPSC:
12352203
eCl@ss:
32160702
NACRES:
NA.41

origen biológico

rabbit

Nivel de calidad

forma del anticuerpo

purified immunoglobulin

tipo de anticuerpo

primary antibodies

clon

polyclonal

reactividad de especies

rat, mouse

envase

antibody small pack of 25 μg

fabricante / nombre comercial

Upstate®

técnicas

western blot: suitable

isotipo

IgG

Nº de acceso NCBI

Nº de acceso UniProt

Condiciones de envío

ambient

modificación del objetivo postraduccional

unmodified

Información sobre el gen

mouse ... Mecp2(17257)
rat ... Mecp2(29386)

Descripción general

NA methyltransferases methylate the 5-position of cytosine in the context of CpG dinucleotides. DNA methylation is crucial for normal embryonic development, imprinting, and X chromosome inactivation. Methyl CpG binding proteins (MeCPs) specifically recognize methylated regions of DNA and repress transcription both directly and by association with known corepressor proteins which include members of the histone deacetylase protein families.

Especificidad

Predicted to cross-react with human based on the conservation of the immunogenic sequence.
Recognizes MeCP2, Mr 75 kDa. A protein at ~75 kDa was also observed in HeLa nuclear extract. This protein was competed by pre-incubation of the antibody with the immunogenic peptide, suggesting that some HeLa strains contain MeCP2 or a related protein, contrary to a previous report.

Inmunógeno

KLH-conjugated, synthetic peptide corresponding to amino acids 465-478 of mouse MeCP2 (C-PRPNREEPVDSRTP) with an N-terminal cysteine added for conjugation purposes.

Aplicación

Research Category
Epigenetics & Nuclear Function
Research Sub Category
Histones
Use Anti-MeCP2 Antibody (rabbit polyclonal antibody) validated in WB to detect MeCP2 also known as MeCP-2 protein, mental retardation X-linked 16, mental retardation X-linked 79, methyl CpG binding protein 2.

Calidad

Evaluated by Western Blot on Mouse Brain lysates.

Descripción de destino

~75 kDa observed

Forma física

Format: Purified
Protein A purified
Purified rabbit polyclonal IgG in buffer containing 0.1 M Tris-glycine, pH 7.4, 0.15 M NaCl, 0.05% sodium azide.

Almacenamiento y estabilidad

Stable for 1 year at 2-8°C from date of receipt.

Nota de análisis

Control
Mouse Brain lysate.

Otras notas

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Información legal

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

Cláusula de descargo de responsabilidad

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Referencia del producto
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Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Visite la Librería de documentos

A WW domain binding region in methyl-CpG-binding protein MeCP2: impact on Rett syndrome.
Jan P Buschdorf, Wolf H Stratling
Journal of Molecular Medicine null
MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome.
M Wan, K Zhao, S S Lee, U Francke
Human Molecular Genetics null
The methyl-CpG-binding protein MeCP2 links DNA methylation to histone methylation.
Fuks, F; Hurd, PJ; Wolf, D; Nan, X; Bird, AP; Kouzarides, T
The Journal of Biological Chemistry null
SKI promotes Smad3 linker phosphorylations associated with the tumor-promoting trait of TGFbeta.
Lin, Q; Chen, D; Timchenko, NA; Medrano, EE
Cell Cycle null
Ocular MECP2 protein expression in patients with and without Rett syndrome.
Jain D, Singh K, Chirumamilla S, Bibat GM, Blue ME, Naidu SR, Eberhart CG
Pediatric Neurology null

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