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17-229

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Acetyl-Histone H4 Immunoprecipitation (ChIP) Assay Kit

Acetyl-Histone H4 Immunoprecipitation (ChIP) Assay Kit used to immunoprecipitate transcriptionally active chromatin from mammalian cells using anti-Acetyl-Histone H4, ChIP grade rabbit antiserum.

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About This Item

Código UNSPSC:
12161503
eCl@ss:
32161000
NACRES:
NA.52

Nivel de calidad

fabricante / nombre comercial

Upstate®

técnicas

immunoprecipitation (IP): suitable

Nº de acceso NCBI

Nº de acceso UniProt

Condiciones de envío

dry ice

Descripción general

For use to immunoprecipitate transcriptionally active chromatin from mammalian cells using anti-Acetyl-Histone H4, ChIP grade rabbit antiserum. Detection of the gene or promoter of interest in immunoprecipitated chromatin must be empirically determined by the researcher using quantitative PCR or Southern slot-blot analysis, using promotor specific primers or probe.

Aplicación

Acetyl-Histone H4 Immunoprecipitation (ChIP) Assay Kit used to immunoprecipitate transcriptionally active chromatin from mammalian cells using anti-Acetyl-Histone H4, ChIP grade rabbit antiserum.

Envase

Kit capacity: 22 assays

Componentes

Anti-acetyl-Histone H4 (Cat.# 06-866)

Protein A agarose/Salmon Sperm DNA (Cat.# 16-157)

All necessary buffers

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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Palabra de señalización

Warning

Frases de peligro

Clasificaciones de peligro

Aquatic Chronic 3 - Eye Irrit. 2

Código de clase de almacenamiento

10 - Combustible liquids


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Guocheng He et al.
Molecular and cellular biology, 22(9), 2965-2973 (2002-04-10)
Repression of human immunodeficiency virus type 1 (HIV-1) transcription may contribute to the establishment or maintenance of proviral quiescence in infected CD4(+) cells. The host factors YY1 and LSF cooperatively recruit histone deacetylase 1 (HDAC1) to the HIV-1 long terminal
Hui Liu et al.
Blood, 104(8), 2505-2513 (2004-07-01)
Cyclin D1 expression is deregulated by chromosome translocation in mantle cell lymphoma and a subset of multiple myeloma. The molecular mechanisms involved in long-distance gene deregulation remain obscure, although changes in acetylated histones and methylated CpG dinucleotides may be important.
Shaojing Chang et al.
Journal of immunology (Baltimore, Md. : 1950), 181(12), 8372-8381 (2008-12-04)
Forming and removing epigenetic histone marks at gene loci are central processes in differentiation. Here, we explored mechanisms establishing long-range H4 acetylation marks at the Ifng locus during Th1 lineage commitment. In Th0 cells, histone deacetylase (HDAC)-Sin3A complexes recruited to
Lata Balakrishnan et al.
Journal of molecular biology, 365(1), 18-30 (2006-10-24)
SV40 chromosomes undergoing transcription operationally defined by the presence of RNA polymerase II (RNAPII) were immune-selected with antibody to RNAPII and subjected to secondary chromatin immunoprecipitation with antibodies to hyperacetylated or unacetylated H4 or H3. Immune selection fragmentation and immunoprecipitation
Melker Göransson et al.
International journal of cancer, 115(4), 556-560 (2005-02-03)
The myxoid/round cell liposarcoma oncogene FUS-DDIT3 is the result of a translocation derived gene fusion between the splicing factor FUS and DDIT3. In order to investigate the downstream targets of DDIT3, and the transforming effects of the FUS-DDIT3 fusion protein

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