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05-928

Sigma-Aldrich

Anti-Histone H3 Antibody, CT, pan, clone A3S, rabbit monoclonal

clone A3S, Upstate®, from rabbit

同義詞:

H3, Histone H3, H3 histone, family 3A

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About This Item

分類程式碼代碼:
12352203
eCl@ss:
32160702
NACRES:
NA.41

生物源

rabbit

品質等級

抗體表格

purified antibody

抗體產品種類

primary antibodies

無性繁殖

A3S, monoclonal

物種活性

Saccharomyces cerevisiae, mouse, chicken, yeast, human, rat

製造商/商標名

Upstate®

技術

ChIP: suitable
western blot: suitable

同型

IgG

NCBI登錄號

UniProt登錄號

運輸包裝

wet ice

目標翻譯後修改

unmodified

基因資訊

human ... H3F3B(3021)

一般說明

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.

特異性

Broad species cross-reactivity expected due to sequence homology.
Recognizes Histone H3, Mr 17 kDa

免疫原

KLH-conjugated, synthetic peptide corresponding to the C-terminus of human Histone H3.

應用

Chromatin Immunoprecipitation:
2 μL of this antibody immunoprecipitated chromatin associated with Histone H3 from a wild type yeast lysate.
Use Anti-Histone H3 Antibody, CT, pan, clone A3S (Rabbit Monoclonal Antibody) validated in ChIP, WB to detect Histone H3 also known as Histone H3.

品質

Routinely evaluated by western blot analysis.

Western Blot Analysis:
1:2,000-1:20,000 dilution of this lot detected Histone H3 in a modification independent manner in acid extracted proteins from untreated, sodium butyrate or colcemid treated HeLa cells.

標靶描述

17 kDa

外觀

Format: Purified
Purified rabbit monoclonal IgG in buffer containing 0.014 M phosphate buffer, pH 7.6, 0.175 M NaCl, 0.07% sodium azide and 30% glycerol.

儲存和穩定性

Stable for 1 year at -20ºC 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. Note: Variability in freezer temperatures below -20°C may cause glycerol-containing solutions to become frozen during storage.

分析報告

Control
Acid extracted proteins from HeLa cells, HeLa nuclear extracts or acid extracted HeLa cells treated with sodium butyrate.

其他說明

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

法律資訊

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

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儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 2


分析證明 (COA)

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Epichromatin is conserved in Toxoplasma gondii and labels the exterior parasite chromatin throughout the cell cycle.
Vanagas, L; Dalmasso, MC; Dubremetz, JF; Portiansky, EL; Olins, DE; Angel, SO
Parasitoloty null
Soraya Bravo et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 21(7), 1403-1412 (2013-05-29)
Cancer development involves changes driven by the epigenetic machinery, including nucleosome positioning. Recently, the concept that adenoviral replication may be driven by tumor specific promoters (TSPs) gained support, and several conditionally replicative adenoviruses (CRAd) exhibited therapeutic efficacy in clinical trials.
Jamie Benoit et al.
Brain structure & function, 221(8), 3963-3978 (2015-11-04)
Histone acetylation is considered a major epigenetic process that affects brain development and synaptic plasticity, as well as learning and memory. The transcriptional effectors and morphological changes responsible for plasticity as a result of long-term modifications to histone acetylation are
The death-associated protein DAXX is a novel histone chaperone involved in the replication-independent deposition of H3.3.
Drane P, Ouararhni K, Depaux A, Shuaib M, Hamiche A
Genes & Development null
Vijay S Thakur et al.
Carcinogenesis, 33(2), 377-384 (2011-11-25)
Green tea polyphenols (GTPs) reactivate epigenetically silenced genes in cancer cells and trigger cell cycle arrest and apoptosis; however, the mechanisms whereby these effects occur are not well understood. We investigated the molecular mechanisms underlying the antiproliferative effects of GTP

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