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Key Documents

ABE460

Sigma-Aldrich

Anti-dimethyl Histone H3 (Arg2), symmetric Antibody

serum, from rabbit

Synonyme(s) :

H3R2me2s, Histone H3/a, Histone H3/b, Histone H3/c, Histone H3/d, Histone H3/f, Histone H3/h, Histone H3/i, Histone H3/j, Histone H3/k, Histone H3/l

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About This Item

Code UNSPSC :
12352203
eCl@ss :
32160702
Nomenclature NACRES :
NA.41

Source biologique

rabbit

Niveau de qualité

Forme d'anticorps

serum

Type de produit anticorps

primary antibodies

Clone

polyclonal

Espèces réactives

human

Réactivité de l'espèce (prédite par homologie)

mouse (based on 100% sequence homology), rat (based on 100% sequence homology)

Technique(s)

ChIP: suitable
dot blot: suitable
immunohistochemistry: suitable
western blot: suitable

Numéro d'accès NCBI

Numéro d'accès UniProt

Conditions d'expédition

wet ice

Modification post-traductionnelle de la cible

dimethylation (Arg2)

Informations sur le gène

human ... HIST1H3F(8968)

Description générale

Histones are highly conserved proteins that serve as the structural scaffold for the organization of nuclear DNA into chromatin. The four core histones, H2A, H2B, H3, and H4, assemble into an octamer (2 molecules of each). Subsequently, 146 base pairs of DNA are wrapped around the octamer, forming a nucleosome, the basic subunit of chromatin. Histones are modified post-translationally by the actions of enzymes in both the nucleus and cytoplasm. These modifications regulate DNA transcription, repair, recombination, and replication. The most commonly studied modifications are acetylation, phosphorylation, methylation, and ubiquitination. These modifications can alter local chromatin architecture, or recruit trans-acting factors that recognize specific histone modifications (the "histone code" hypothesis). The modifications occur predominantly on the N-terminal and C-terminal tails that extend beyond the nucleosome core particle.

Immunogène

Epitope: Methylated Arg2
Linear peptide corresponding to human Histone H3 symmetrically dimethylated at Arg2.

Application

Dot Blot (Specificity) Analysis: A 1:1,000 dilution from a representative lot detected Histone H3 (Arg2) in an Absurance Histone H3 Specificity Array (Cat. No. 16-667).

Immunohistochemistry Analysis: A representative lot from an independent laboratory detected Histone H3 (Arg2) in drosophila chromosomes (Migliori, V., et al. (2012). Nat Struct Mol Biol. 19(2):136-144.).

Chromatin Immunoprecipitation Analysis: A representative lot from an independent laboratory immunoprecipitated Histone H3 (Arg2) from P493-6 cell lysate (Migliori, V., et al. (2012). Nat Struct Mol Biol. 19(2):136-144.).
Research Category
Epigenetics & Nuclear Function
Research Sub Category
Histones
This Anti-dimethyl Histone H3 (Arg2) antibody, symmetric is validated for use in western blotting, dot blot, IHC & ChIP for the detection of dimethyl Histone H3 (Arg2).

Qualité

Evaluated by Western Blotting in untreated and nocodazole treated HeLa cell lysate.

Western Blotting Analysis: A 1:1,000 dilution of this antibody detected dimethyl Histone H3 (Arg2) in 10 µg of nocodazole treated HeLa cell lysate and demonstrated a loss of signal in untreated HeLa cell lysate.

Description de la cible

~17 kDa observed. Uncharacterized band(s) may be observed in some cell lysates.

Forme physique

Rabbit polyclonal serum containing 0.05% sodium azide.
Unpurified

Stockage et stabilité

Stable for 1 year at -20°C from date of receipt.
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.

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 1


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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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Yanbo Wang et al.
Scientific reports, 5, 11031-11031 (2015-06-16)
During germ cell development, epigenetic modifications undergo extensive remodeling. Abnormal epigenetic modifications usually result in germ cell loss and reproductive defect. Prmt5 (Protein arginine methyltransferase 5) encodes a protein arginine methyltransferase which has been demonstrated to play important roles in
Yanbo Wang et al.
Biology of reproduction, 92(4), 104-104 (2015-03-27)
In mammals, germ cells undergo massive epigenetic remodeling during fetal development. However, the physiological functions of epigenetic modification in germ cell development remain unclear. In this study, we found that protein arginine methyltransferase 5 (Prmt5) was abundantly expressed in the
Gizem Günes Günsel et al.
Nature communications, 13(1), 1303-1303 (2022-03-16)
Extravasation of monocytes into tissue and to the site of injury is a fundamental immunological process, which requires rapid responses via post translational modifications (PTM) of proteins. Protein arginine methyltransferase 7 (PRMT7) is an epigenetic factor that has the capacity
Ruiqiong Liu et al.
Nucleic acids research, 46(13), 6608-6626 (2018-05-31)
Histone post-translational modifications regulate chromatin structure and function largely through interactions with effector proteins that often contain multiple histone-binding domains. PHF1 [plant homeodomain (PHD) finger protein 1], which contains two kinds of histone reader modules, a Tudor domain and two
Yanli Jin et al.
The Journal of clinical investigation, 126(10), 3961-3980 (2016-09-20)
Imatinib-insensitive leukemia stem cells (LSCs) are believed to be responsible for resistance to BCR-ABL tyrosine kinase inhibitors and relapse of chronic myelogenous leukemia (CML). Identifying therapeutic targets to eradicate CML LSCs may be a strategy to cure CML. In the

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