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A propos de cet article
UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Clone:
polyclonal
Species reactivity:
human, vertebrates
Application:
ELISA, ICC, WB, inhibition assay
Citations:
39
Service technique
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Laissez-nous vous aiderbiological source
rabbit
Quality Level
antibody form
affinity purified immunoglobulin
antibody product type
primary antibodies
clone
polyclonal
purified by
affinity chromatography
species reactivity
human, vertebrates
manufacturer/tradename
Upstate®
technique(s)
ELISA: suitable, immunocytochemistry: suitable, inhibition assay: suitable (peptide), western blot: suitable
isotype
IgG
NCBI accession no.
UniProt accession no.
shipped in
dry ice
target post-translational modification
trimethylation (Arg17)
Gene Information
human ... H3C1(8350)
General description
L'histone H3.1t (UniProt : Q16695; also known as H3/t, H3tm, H3/g) is encoded by the HIST3H3 (also known as H3FT) gene (Gene ID: 8290) chez l'être humain. Histone H3 has two main variants, H3.1 and H3.3, which show different genomic localization patterns in animals. The H3.1 and H3.3 complexes also possess distinct histone chaperones, CAF-1 and HIRA, which play important role in mediating DNA-synthesis-dependent and -independent nucleosome assembly. It has been reported that Histone H3.1 serves as the canonical histone, which is incorporated during DNA replication, whereas H3.3 acts as the replacement histone that can be incorporated outside of S-phase during chromatin-disrupting processes like transcription. Histone H 3.1 is a core component of nucleosome that is present only in mammals and is usually enriched in acetylation of Lysine 15 and demethylation of lysine 10 (HeK9Me2). It is expressed during S phase, then expression decreases significantly as cell division slows down during the process of differentiation. Histone H 3.1 expression is shown to be replication dependent. It s presence at the site of UV-induced DNA damage has also been reported. It has also been shown that H3.1/H4 tetramers do not split and remain intact during replication dependent deposition of H3.1 variant. Dimethylation of H3 on Arginine 17 has been linked to gene activation and activation of this modification is linked to cell fate regulation and increases the pluripotency potential of stem cells. In pancreatic beta cells expression of Protein arginine methyltransferase 4 (PRMT4) and demethylation of Arginine 17 is shown to increase under high glucose conditions. (réf. : Kim, JK et al. (2015). J. Mol. Endocrinol. 54(3); 315-24).
Poids réel (observé) : env. 17 kDa ; poids théorique (calculé) : 15,51 kDa. Des bandes non caractérisées peuvent être observées avec certains lysats.
Immunogen
BSA-conjugated linear peptide corresponding to 11 amino acids from the N-terminal region of human Histone H3 dimethylated on Arginine 17 (methionine removed).
Application
&&
Domaine de recherche
Épigénétique et fonction nucléaire
Épigénétique et fonction nucléaire
Peptide Inhibition Assay Analysis/Western Blotting: A 1:7,500 dilution from a representative lot detected dimethyl-Histone H3 (Arg17) in Histone H3 with CARM1.
un précédent lot de cet anticorps a été utilisé en ELISA. At dilutions greater than 1:2000 this antibody is specific for peptides containing dimethylated Arg17.
An independent laboratory showed positive immunostaining for CARM-1 specific methylation of Histone H3 in 3134 cells.
un précédent lot de cet anticorps a été utilisé en ELISA. At dilutions greater than 1:2000 this antibody is specific for peptides containing dimethylated Arg17.
An independent laboratory showed positive immunostaining for CARM-1 specific methylation of Histone H3 in 3134 cells.
Sous-domaine de recherche
Histones
Histones
Biochem/physiol Actions
Broad cross-reactivity expected based on sequence homology among species.
This rabbit polyclonal antibody specifically detects human Histone H3 dimethylated on Arginine 17.
Physical form
Anticorps polyclonal de lapin purifié, dans un tampon à base de Tris-glycine 0,1 M (pH 7,4) et de NaCl 150 mM contenant 0,05 % d'azoture de sodium.
Chromatographie d'immuno-affinité
Preparation Note
Stable à -20 °C pendant 1 an à compter de la date de réception. Recommandations relatives à la manipulation du produit : dès réception, et avant le retrait du bouchon, centrifuger le flacon et mélanger délicatement la solution. Répartir en aliquotes dans des microtubes à centrifuger et conserver ces derniers à -20 °C. Éviter les congélations/décongélations répétées, qui peuvent détériorer les IgG et nuire aux performances du produit.
Analysis Note
A 1:7,500 dilution of this antibody detected dimethyl-Histone H3 (Arg17) in Histone H3 treated with Histone-arginine methyltransferase (CARM1).
Other Notes
Concentration : pour connaître la concentration spécifique du lot, voir le certificat d'analyse.
Legal Information
UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
Sauf indication contraire dans notre catalogue ou toute autre documentation associée au(x) produit(s), nos produits sont uniquement destinés à la recherche et ne sauraient être utilisés à d'autres fins, ce qui inclut, sans s'y limiter, les utilisations commerciales non autorisées, les utilisations diagnostiques in vitro, les utilisations thérapeutiques ex vivo ou in vivo, ou tout type de consommation ou d'application chez l'être humain ou chez l'animal.
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Classe de stockage
12 - Non Combustible Liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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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Coactivator-associated arginine methyltransferase-1 enhances nuclear factor-kappaB-mediated gene transcription through methylation of histone H3 at arginine 17.
Miao, F; Li, S; Chavez, V; Lanting, L; Natarajan, R
Molecular Endocrinology null
Donghang Cheng et al.
Molecular cell, 25(1), 71-83 (2007-01-16)
The coactivator-associated arginine methyltransferase CARM1 is recruited by many different transcription factors as a positive regulator. To understand the mechanism by which CARM1 functions, we sought to isolate its substrates. We developed a small-pool screening approach for this purpose and
Caroline S Dacwag et al.
Molecular and cellular biology, 29(7), 1909-1921 (2009-02-04)
Temporal regulation of gene expression is a hallmark of cellular differentiation pathways, yet the mechanisms controlling the timing of expression for different classes of differentiation-specific genes are not well understood. We previously demonstrated that the class II arginine methyltransferase Prmt5
Numéro d'article de commerce international
| Référence | GTIN |
|---|---|
| 07-214 | 04053252515095 |