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Merck
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Documentos Principais

16-222

Sigma-Aldrich

Anti-Phospho-Histone H3 (Ser10) Antibody, clone 3H10, FITC Conjugate

clone 3H10, Upstate®, from mouse

Sinônimo(s):

H3 histone, family 3A, H3S10P, Histone H3 (phospho S10), H3 histone, family 3A, H3 histone, family 3B, H3 histone, family 3B (H3.3B)

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About This Item

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

fonte biológica

mouse

Nível de qualidade

conjugado

FITC conjugate

forma do anticorpo

purified antibody

tipo de produto de anticorpo

primary antibodies

clone

3H10, monoclonal

reatividade de espécies

human

fabricante/nome comercial

Upstate®

técnica(s)

immunocytochemistry: suitable
immunofluorescence: suitable
western blot: suitable

Isotipo

IgG

nº de adesão NCBI

nº de adesão UniProt

Condições de expedição

wet ice

modificação pós-traducional do alvo

phosphorylation (pSer10)

Informações sobre genes

human ... HIST1H3F(8968)

Descrição geral

Histone H3 is one of the five main histone proteins involved in the structure of chromatin in eukaryotic cells. Featuring a main globular domain and a long N-terminal tail, H3 is involved with the structure of the nucleosomes of the ′beads on a string′ structure. The N-terminal tail of histone H3 protrudes from the globular nucleosome core and can undergo several different types of epigenetic modifications that influence cellular processes. These modifications include the covalent attachment of methyl or acetyl groups to lysine and arginine amino acids and the phosphorylation of serine or threonine.

Especificidade

Broad species cross-reactivity is expected.
Recognizes histone H3 phosphorylated at Ser10, MW 17 kDa.

Imunogênio

A proprietary immunogen based on a peptide sequence containing phospho-serine corresponding to residue 10 of human histone H3. Clone 3H10.
Epitope: Ser10

Aplicação

Anti-Phospho-Histone H3 (Ser10) Antibody, clone 3H10, FITC Conjugate is a Mouse Monoclonal for detection of Histone H3 phosphorylated at serine 10. This mAb, also known as H3S10p,is labeled with Fluorescein isothiocyanate (FITC), published in peer reviewed journals & validated in WB, ICC & IF.
Research Category
Epigenetics & Nuclear Function
Research Sub Category
Histones
Western Blot Analysis: 0.5-5 µg/mL of this lot detected phosphorylated histone H3 in acid extracted proteins from mitotic HeLa cells (Catalog # 17-306) treated with colcemid.

Qualidade

Immunocytochemistry: Mitotic HeLa cells showed positive chromosome staining with 4μg/mL of this antibody.

Descrição-alvo

17 kDa

forma física

Protein G Purified
Purified mouse monoclonal IgG in buffer containing PBS with 0.05% sodium azide, pH7.1.

Armazenamento e estabilidade

Stable for 1 year at from date of receipt.

Nota de análise

Control
Mitotic HeLa cells (IF).

Informações legais

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

Exoneração de responsabilidade

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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Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 2


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Tumor-suppressing function of caspase-2 requires catalytic site Cys-320 and site Ser-139 in mice.
Keqin Ren,Jing Lu,Aleksey Porollo,Chunying Du
The Journal of Biological Chemistry null
Antje M Wengner et al.
Molecular cancer therapeutics, 15(4), 583-592 (2016-02-03)
Monopolar spindle 1 (Mps1) has been shown to function as the key kinase that activates the spindle assembly checkpoint (SAC) to secure proper distribution of chromosomes to daughter cells. Here, we report the structure and functional characterization of two novel
Agata Zieba et al.
Molecular & cellular proteomics : MCP, 11(7), M111-M111 (2012-03-24)
Fundamental open questions in signal transduction remain concerning the sequence and distribution of molecular signaling events among individual cells. In this work, we have characterized the intercellular variability of transforming growth factor β-induced Smad interactions, providing essential information about TGF-β

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