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H0788

Sigma-Aldrich

Monoclonal Anti-acetyl- & phospho-Histone H3 (Ac-Lys9, pSer10) antibody produced in mouse

~2 mg/mL, clone APH3-64, purified immunoglobulin, buffered aqueous solution

Synonyme(s) :

Anti-H3K9acS10p

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About This Item

Numéro MDL:
Code UNSPSC :
12352203
Nomenclature NACRES :
NA.41

Source biologique

mouse

Conjugué

unconjugated

Forme d'anticorps

purified immunoglobulin

Type de produit anticorps

primary antibodies

Clone

APH3-64, monoclonal

Forme

buffered aqueous solution

Poids mol.

antigen ~17 kDa

Espèces réactives

Drosophila, bovine, chicken, rat, mouse, human, frog, Caenorhabditis elegans

Concentration

~2 mg/mL

Technique(s)

immunoprecipitation (IP): suitable
indirect ELISA: suitable
microarray: suitable
western blot: suitable using whole cell extract of Jurkat cell line treated with nocodazole

Isotype

IgG2a

Numéro d'accès UniProt

Conditions d'expédition

dry ice

Température de stockage

−20°C

Modification post-traductionnelle de la cible

acetylation (Lys9), phosphorylation (pSer10)

Description générale

Monoclonal Anti-Acetyl & Phospho-Histone H3 (Ac-Lys9, pSer10) (mouse IgG2a isotype) is derived from the APH3-64 hybridoma produced by the fusion of mouse myeloma cells (NS1) and splenocytes from BALB/c mice immunized with a synthetic, acetylated and phosphorylated histone H3 peptide. Histone H3 is a component of the histone octamer of the nucleosome DNA complex. It possesses a lysine-rich N-terminal tail region.

Spécificité

Monoclonal Anti-Acetyl & Phospho-Histone H3 (Ac-Lys, pSer) specifically recognizes human histone H3 only when simultaneously acetylated on Lys and phosphorylated at Ser.

Immunogène

synthetic, acetylated and phosphorylated histone H3 peptide (amino acids 7-20, Ac-Lys9, pSer10) corresponding to the N-terminus of human histone H3. The sequence is identical in many species.

Application

Monoclonal Anti-acetyl- & phospho-Histone H3 (Ac-Lys9, pSer10) antibody produced in mouse has been used in:
  • chromatin immunoprecipitation
  • antibody microarray
  • enzyme-linked immunosorbent assay (ELISA)
  • immunoblotting
  • immunoprecipitation

Actions biochimiques/physiologiques

Acetylation of histones on lysine residues within the N-terminal domain by histone acetyl-transferase (HATs) including histone acetyltransferase (Gcn5p), p300/CREB-binding protein-associated factor (P/CAF), E1A binding protein p300/CREB-binding protein (p300/CBP), and transcription initiation factor TFIID 250 kDa subunit (TAFII250) is associated with transcriptional activation. This modification results in remodeling of the nucleosome structure making it more accessible to transcription complexes. In most species, histone H3 is primarily acetylated at lysines 9, 14, 18, and 23. In some organisms, acetylation at lysine 9 appears to have a dominant role in histone deposition and chromatin assembly. Phosphorylation of histone H3 on Ser10 is tightly correlated with chromosome condensation during both mitosis and meiosis. Phosphorylation at serine is implicated with the induction of immediate-early oncogenes like c-jun, c-fos, and c-myc. Protein kinase A (PKA), 90 kDa ribosomal S6 kinase-2 (Rsk-2), and MAP- and Stress-activated kinase 1 (Msk-1) are necessary for histone H3 phosphorylation. The ERK and p38 pathways activate Msk-1 to phosphorylate histone H3. Monoclonal antibodies to acetylated and phosphorylated histone H3 are an important tool for studying chromatin remodeling and gene regulation.

Forme physique

Solution 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

Stockage et stabilité

For continuous use, store at 2-8 °C for up to one month. For extended storage, freeze in working aliquots at −20 °C. Repeated freezing and thawing is not recom-mended. Storage in “frost-free” freezers is also not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if not used within 12 hours.

Clause de non-responsabilité

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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Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Consulter la Bibliothèque de documents

Christian Meinert et al.
Data in brief, 10, 354-363 (2016-12-27)
In 2016, Meinert et al. (doi: 10.1016/j.jprot.2015.09.020) published the first 25 proteins in a protein array regulated in Human Umbilical Vein Endothelial Cells (HUVEC) by the heptapeptide angiotensin (Ang)-(1-7) and the first 10 intracellular signaling cascades at different time points.
D E Sterner et al.
Microbiology and molecular biology reviews : MMBR, 64(2), 435-459 (2000-06-06)
The state of chromatin (the packaging of DNA in eukaryotes) has long been recognized to have major effects on levels of gene expression, and numerous chromatin-altering strategies-including ATP-dependent remodeling and histone modification-are employed in the cell to bring about transcriptional
Signaling to chromatin through histone modifications.
P Cheung et al.
Cell, 103(2), 263-271 (2000-11-01)
Anne-Marie Baird et al.
PloS one, 6(1), e14593-e14593 (2011-02-08)
Angiogenesis may play a role in the pathogenesis of Non-Small Cell Lung cancer (NSCLC). The CXC (ELR(+)) chemokine family are powerful promoters of the angiogenic response. The expression of the CXC (ELR(+)) family members (CXCL1-3/GROα-γ, CXCL8/IL-8, CXCR1/2) was examined in
B D Strahl et al.
Nature, 403(6765), 41-45 (2000-01-19)
Histone proteins and the nucleosomes they form with DNA are the fundamental building blocks of eukaryotic chromatin. A diverse array of post-translational modifications that often occur on tail domains of these proteins has been well documented. Although the function of

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