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Merck

06-1358

Anti-acetyl (Lys34) phospho (Ser36) Histone H1 Antibody

from rabbit, purified by affinity chromatography

Sinonimo/i:

Histone H1.4, Histone H1b

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Informazioni su questo articolo

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

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Origine biologica

rabbit

Livello qualitativo

Forma dell’anticorpo

affinity isolated antibody

Tipo di anticorpo

primary antibodies

Clone

polyclonal

Purificato mediante

affinity chromatography

Reattività contro le specie

human, bovine

Reattività contro le specie (prevista in base all’omologia)

canine (based on 100% sequence homology), rhesus macaque (based on 100% sequence homology)

tecniche

dot blot: suitable
western blot: suitable

N° accesso NCBI

N° accesso UniProt

Condizioni di spedizione

wet ice

modifica post-traduzionali bersaglio

phosphorylation (pSer36), acetylation (Lys34)

Informazioni sul gene

bovine ... H1-4(617854)
dog ... H1-4(488269)
human ... H1-4(3008)
rhesus monkey ... H1-4(696872)

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Questo articolo
06-137205-45707-353
species reactivity

human, bovine

species reactivity

human

species reactivity

bovine, human, plant

species reactivity

Saccharomyces cerevisiae, yeast, human

biological source

rabbit

biological source

rabbit

biological source

mouse

biological source

rabbit

clone

polyclonal

clone

polyclonal

clone

AE-4, monoclonal

clone

polyclonal

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

purified immunoglobulin

antibody form

serum

shipped in

wet ice

shipped in

wet ice

shipped in

dry ice

shipped in

dry ice

Gene Information

bovine ... H1-4(617854)
dog ... H1-4(488269)
human ... H1-4(3008)
rhesus monkey ... H1-4(696872)

Gene Information

dog ... H1-4(488269)
human ... H1-4(3008)
rhesus monkey ... H1-4(696872)

Gene Information

bovine ... H1-4(617854)
human ... H1-4(3008)

Gene Information

human ... H3C1(8350)

Descrizione generale

H1.4 is one of four variants of histone H1 (H1.2-H1.5) that is found in somatic cells. The H1 histones may function as linker proteins binding DNA via their GH domain, and enabling the wrapping of DNA around the core nucleosomal structure formed from the association of H2A, H2B, H3, and H4. In response to various stimuli, histones undergo a number of post-translational modifications (PTM) including acetylation, phoshorylation, and methylation. Previous studies have suggested that H1.4 may be phosphorylated during mitosis and interphase resulting in increased transcription of target genes by RNA polymerase I and II, and therefore this PTM on H1.4 may have implications for cell growth. H1.4 may also undergo acetylation of its N-terminal lysine residues. Often, it is the pattern of different modifications on several histone residues that alter chromatin and affect gene expression, rather than modification of single residues.
~34 kDa observed

Immunogeno

Epitope: Acetylated Lys34 and phosphorylated Ser36
KLH-conjugated linear peptide corresponding to human Histone H1 acetylated at Lys34 and phosphorylated at Ser36.

Applicazioni

Dot Blot Specificity Analysis: Unmodified and various modified Histone peptides (see Table) were probed with acetyl (Lys34) phospho (Ser36) Histone H1.
Research Category
Epigenetics & Nuclear Function
Research Sub Category
Histones
Use Anti-acetyl (Lys34) phospho (Ser36) Histone H1 Antibody (Rabbit Polyclonal Antibody) validated in WB & DB to detect acetyl (Lys34) phospho (Ser36) Histone H1 also known as Histone H1b.

Azioni biochim/fisiol

Other homologies: Mouse and Rat (90% sequence homology).
This antibody recognizes Histone H1 acetylated at Lys34 and phosphorylated at Ser36.

Stato fisico

Affinity purified
Purified rabbit polyclonal in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Nota sulla preparazione

Stable for 1 year at 2-8°C from date of receipt.

Risultati analitici

Control
Calf thymus histone extract
Evaluated by Western Blot in calf thymus histone extract.

Western Blot Analysis: A 1:37 dilution of this antibody detected Histone H1 on 10 µg of calf thymus histone extract.

Altre note

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Esclusione di responsabilità

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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Codice della classe di stoccaggio

12 - Non Combustible Liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Contenuto correlato

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).

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