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Merck

07-371

Anti-Histone H2B Antibody

Upstate®, from rabbit

Synonyme(s) :

H2B, Histone H2B, H2B histone family, member Q, histone 2, H2be, histone cluster 2, H2be

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A propos de cet article

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
polyclonal
Application:
WB
Citations:
165
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biological source

rabbit

conjugate

unconjugated

antibody form

purified antibody

antibody product type

primary antibodies

clone

polyclonal

species reactivity

human, chicken

species reactivity (predicted by homology)

yeast (based on 100% sequence homology), Xenopus (based on 100% sequence homology)

manufacturer/tradename

Upstate®

technique(s)

western blot: suitable

isotype

IgG

NCBI accession no.

UniProt accession no.

shipped in

dry ice

target post-translational modification

unmodified

Quality Level

Gene Information

Saccharomyces cerevisiae ... Htb2(852284)
human ... H2BC1(255626)

General description

Histone H2B type 3-B (UniProt: Q8N257; also known as H2B type 12) is encoded by the HIST3H2BB gene (Gene ID: 128312) chez l'être humain. Histones are basic nuclear proteins that are responsible for the nucleosome structure of chromatin in eukaryotes. Deux molécules de chacune des quatre histones fondamentales (H2A, H2B, H3 et H4) forment un octamère autour duquel l'ADN est enroulé sous forme d'unités répétitives appelées nucléosomes. Ceci limite l'accès de la machinerie cellulaire à l'ADN, dont elle a besoin comme matrice. Les histones jouent donc un rôle central dans la régulation de la transcription, la réparation de l'ADN, la réplication de l'ADN et la stabilité chromosomique. L'accessibilité de l'ADN est régulée par l'intermédiaire d'un ensemble complexe de modifications post-traductionnelles des histones, aussi appelé code des histones, et du remodelage des nucléosomes. Histone H2B is one of the main histone proteins involved in the structure of chromatin in eukaryotic cells. ′′ Histone H2B can be monoubiquitinated on Lysine123 by RAD6/UBC2-BRE1 complex to form H2BK123Ub1 complex that gives a specific tag for epigenetic transcriptional activation and is also a prerequisite for H3K4me and H3K79me formation. H2BK123ub1 is reported to modulates the formation of double-strand breaks during meiosis and is a required for DNA-damage checkpoint activation. Histone H2B is phosphorylated by STE20 to form H2BS10ph during progression through meiotic prophase and may be correlated with chromosome condensation. Histone H2B can undergo acetylation by GCN5, a component of the SAGA complex, to form H2BK11ac and H2BK16ac. Acetylation of N-terminal lysines and particularly formation of H2BK11acK16ac has a positive effect on transcription.
Poids réel (observé) : env. 17 kDa ; poids théorique (calculé) : 13,91 kDa. Des bandes non caractérisées peuvent être observées avec certains lysats.

Immunogen

KLH-conjugated linear peptide corresponding to 9 amino acids from the C-terminus of human Histone H2B type 3-B.

Application

Analyse par western blotting : µ
Anti-Histone H2B Antibody, Cat. No. 07-371, is a highly specific rabbit polyclonal antibody that targets Histone H2B and has been tested in Western Blotting.
Domaine de recherche
Épigénétique et fonction nucléaire
Sous-domaine de recherche
Histones

Biochem/physiol Actions

This rabbit polyclonal antibody detects Histone H2B in human and chicken. It targets an epitope within 9 amino acids from the C-terminus region.

Physical form

Chromatographie sur protéine A
Format : Produit purifié
Purified rabbit polyclonal antibody in buffer containing 0.02 M phosphate buffer, pH 7.6, 0.25 M NaCl, with 0.1% sodium azide and 30% glycerol.

Preparation Note

Stable à -20 ºC pendant 1 an à compter de la date de réception.

Analysis Note



µ

Other Notes

Concentration : pour connaître la concentration spécifique du lot, voir le certificat d'analyse.
Remplace le(s) produit(s) suivant(s) : MABE15

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

10 - Combustible liquids

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

Histone variant macroH2A1 deletion in mice causes female-specific steatosis.
Boulard, M; Storck, S; Cong, R; Pinto, R; Delage, H; Bouvet, P
Epigenetics & Chromatin null
Miia M Rytinki et al.
Cellular and molecular life sciences : CMLS, 68(19), 3219-3232 (2011-01-22)
Small ubiquitin-related modifiers (SUMOs) are important regulator proteins. Caenorhabditis elegans contains a single SUMO ortholog, SMO-1, necessary for the reproduction of C. elegans. In this study, we constructed transgenic C. elegans strains expressing human SUMO-1 under the control of pan-neuronal
Mary G Rhoads et al.
European journal of cancer (Oxford, England : 1990), 46(1), 191-197 (2009-10-28)
The mechanisms eliciting cancer cachexia are not well understood. Wasting of skeletal muscle is problematic because it is responsible for the clinical deterioration in cancer patients and for the ability to tolerate cancer treatment. Studies done on animals suggest that
Lietta Nicolaides et al.
Virology, 414(2), 137-145 (2011-04-15)
The E6 protein from high-risk human papillomaviruses appears necessary for persistence of viral episomes in cells but the underlying mechanism is unclear. E6 has many activities, including its ability to bind and degrade PDZ domain-containing proteins, such as hScrib. However
Kaori Fujita et al.
Nature cell biology, 12(12), 1205-1212 (2010-11-09)
The telomere-capping complex shelterin protects functional telomeres and prevents the initiation of unwanted DNA-damage-response pathways. At the end of cellular replicative lifespan, uncapped telomeres lose this protective mechanism and DNA-damage signalling pathways are triggered that activate p53 and thereby induce

Contenu apparenté

Cancer is a complex disease manifestation. At its core, it remains a disease of abnormal cellular proliferation and inappropriate gene expression. In the early days, carcinogenesis was viewed simply as resulting from a collection of genetic mutations that altered the gene expression of key oncogenic genes or tumor suppressor genes leading to uncontrolled growth and disease (Virani, S et al 2012). Today, however, research is showing that carcinogenesis results from the successive accumulation of heritable genetic and epigenetic changes. Moreover, the success in how we predict, treat and overcome cancer will likely involve not only understanding the consequences of direct genetic changes that can cause cancer, but also how the epigenetic and environmental changes cause cancer (Johnson C et al 2015; Waldmann T et al 2013). Epigenetics is the study of heritable gene expression as it relates to changes in DNA structure that are not tied to changes in DNA sequence but, instead, are tied to how the nucleic acid material is read or processed via the myriad of protein-protein, protein-nucleic acid, and nucleic acid-nucleic acid interactions that ultimately manifest themselves into a specific expression phenotype (Ngai SC et al 2012, Johnson C et al 2015). This review will discuss some of the principal aspects of epigenetic research and how they relate to our current understanding of carcinogenesis. Because epigenetics affects phenotype and changes in epigenetics are thought to be key to environmental adaptability and thus may in fact be reversed or manipulated, understanding the integration of experimental and epidemiologic science surrounding cancer and its many manifestations should lead to more effective cancer prognostics as well as treatments (Virani S et al 2012).

Numéro d'article de commerce international

RéférenceGTIN
07-37104053252362811

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