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Merck

H0788

Sigma-Aldrich

Monoclonal Anti-acetyl- & phospho-Histone H3 (Ac-Lys9, pSer10) antibody produced in mouse

~2 mg/mL, clone APH3-64, purified immunoglobulin, buffered aqueous solution

別名:

Anti-H3K9acS10p

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About This Item

MDL番号:
UNSPSCコード:
12352203
NACRES:
NA.41

由来生物

mouse

品質水準

結合体

unconjugated

抗体製品の状態

purified immunoglobulin

抗体製品タイプ

primary antibodies

クローン

APH3-64, monoclonal

形状

buffered aqueous solution

分子量

antigen ~17 kDa

化学種の反応性

Drosophila, bovine, chicken, rat, mouse, human, frog, Caenorhabditis elegans

濃度

~2 mg/mL

テクニック

immunoprecipitation (IP): suitable
indirect ELISA: suitable
microarray: suitable
western blot: suitable using whole cell extract of Jurkat cell line treated with nocodazole

アイソタイプ

IgG2a

UniProtアクセッション番号

輸送温度

dry ice

保管温度

−20°C

ターゲットの翻訳後修飾

acetylation (Lys9), phosphorylation (pSer10)

詳細

Monoclonal Anti-Acetyl & Phospho-Histone H3 (Ac-Lys9, pSer10) (mouse IgG2a isotype) is derived from the APH3-64 hybridoma produced by the fusion of mouse myeloma cells (NS1) and splenocytes from BALB/c mice immunized with a synthetic, acetylated and phosphorylated histone H3 peptide. Histone H3 is a component of the histone octamer of the nucleosome DNA complex. It possesses a lysine-rich N-terminal tail region.

特異性

Monoclonal Anti-Acetyl & Phospho-Histone H3 (Ac-Lys, pSer) specifically recognizes human histone H3 only when simultaneously acetylated on Lys and phosphorylated at Ser.

免疫原

synthetic, acetylated and phosphorylated histone H3 peptide (amino acids 7-20, Ac-Lys9, pSer10) corresponding to the N-terminus of human histone H3. The sequence is identical in many species.

アプリケーション

Monoclonal Anti-acetyl- & phospho-Histone H3 (Ac-Lys9, pSer10) antibody produced in mouse has been used in:
  • chromatin immunoprecipitation
  • antibody microarray
  • enzyme-linked immunosorbent assay (ELISA)
  • immunoblotting
  • immunoprecipitation

生物化学的/生理学的作用

Acetylation of histones on lysine residues within the N-terminal domain by histone acetyl-transferase (HATs) including histone acetyltransferase (Gcn5p), p300/CREB-binding protein-associated factor (P/CAF), E1A binding protein p300/CREB-binding protein (p300/CBP), and transcription initiation factor TFIID 250 kDa subunit (TAFII250) is associated with transcriptional activation. This modification results in remodeling of the nucleosome structure making it more accessible to transcription complexes. In most species, histone H3 is primarily acetylated at lysines 9, 14, 18, and 23. In some organisms, acetylation at lysine 9 appears to have a dominant role in histone deposition and chromatin assembly. Phosphorylation of histone H3 on Ser10 is tightly correlated with chromosome condensation during both mitosis and meiosis. Phosphorylation at serine is implicated with the induction of immediate-early oncogenes like c-jun, c-fos, and c-myc. Protein kinase A (PKA), 90 kDa ribosomal S6 kinase-2 (Rsk-2), and MAP- and Stress-activated kinase 1 (Msk-1) are necessary for histone H3 phosphorylation. The ERK and p38 pathways activate Msk-1 to phosphorylate histone H3. Monoclonal antibodies to acetylated and phosphorylated histone H3 are an important tool for studying chromatin remodeling and gene regulation.

物理的形状

Solution 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

保管および安定性

For continuous use, store at 2-8 °C for up to one month. For extended storage, freeze in working aliquots at −20 °C. Repeated freezing and thawing is not recom-mended. Storage in “frost-free” freezers is also not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if not used within 12 hours.

免責事項

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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保管分類コード

10 - Combustible liquids

WGK

WGK 2

引火点(°F)

Not applicable

引火点(℃)

Not applicable

個人用保護具 (PPE)

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


適用法令

試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。

Jan Code

H0788-200UL:
H0788-VAR:
H0788-BULK:


試験成績書(COA)

製品のロット番号・バッチ番号を入力して、試験成績書(COA) を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。

以前この製品を購入いただいたことがある場合

文書ライブラリで、最近購入した製品の文書を検索できます。

文書ライブラリにアクセスする

Christian Meinert et al.
Data in brief, 10, 354-363 (2016-12-27)
In 2016, Meinert et al. (doi: 10.1016/j.jprot.2015.09.020) published the first 25 proteins in a protein array regulated in Human Umbilical Vein Endothelial Cells (HUVEC) by the heptapeptide angiotensin (Ang)-(1-7) and the first 10 intracellular signaling cascades at different time points.
Anne-Marie Baird et al.
PloS one, 6(1), e14593-e14593 (2011-02-08)
Angiogenesis may play a role in the pathogenesis of Non-Small Cell Lung cancer (NSCLC). The CXC (ELR(+)) chemokine family are powerful promoters of the angiogenic response. The expression of the CXC (ELR(+)) family members (CXCL1-3/GROα-γ, CXCL8/IL-8, CXCR1/2) was examined in
Anne-Marie Baird et al.
Frontiers in oncology, 3, 162-162 (2013-06-27)
The Interleukin-23 (IL-23)/IL-23R signaling axis is an important inflammatory pathway, involved in the stimulation and regulation of the T helper (Th) 17 lymphocytes, resulting in the production of IL-17. Aside from auto-immunity, this cytokine has also been linked to carcinogenesis
B D Strahl et al.
Nature, 403(6765), 41-45 (2000-01-19)
Histone proteins and the nucleosomes they form with DNA are the fundamental building blocks of eukaryotic chromatin. A diverse array of post-translational modifications that often occur on tail domains of these proteins has been well documented. Although the function of
Signaling to chromatin through histone modifications.
P Cheung et al.
Cell, 103(2), 263-271 (2000-11-01)

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