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Merck

16-157

プロテインAアガロース/サケ精子DNA、2.5 mL

for use in chromatin immunoprecipitations (ChIP assays)

別名:

ChIP agarose beads, ChIP agaraose A beads, ChIP assays

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この商品について

UNSPSC Code:
12352202
NACRES:
NA.32
eCl@ss:
32160405
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製品名

プロテインAアガロース/サケ精子DNA、2.5 mL, for use in chromatin immunoprecipitations (ChIP assays)

biological source

Staphylococcus aureus

form

liquid

manufacturer/tradename

Upstate®

technique(s)

ChIP: suitable

suitability

suitable for immunoprecipitation

shipped in

wet ice

Quality Level

Analysis Note

アセチル化ヒストンに架橋されたDNAを切断することにより、クロマチン免疫沈降で定常的に評価済み。その後の検出は、抗アセチルヒストンH4 ChIPグレード(06-866)を用いて実施

Application

クロマチン免疫沈降(ChIP)アッセイでの使用に適しています

General description

超音波処理したサケ精子DNAを含むアルキルアミン結合によりアガロースに共有結合させたプロテインA。 サケ精子DNAは、クロマチンIP(ChIP)アッセイに使用するビーズとの非特異的相互作用を阻害します。ChIPキットに含まれる部品番号16-157Cは別途入手できないことに注意し、16-157を購入してください。
黄色ブドウ球菌由来のプロテインAは、IgG分子のFc領域に非常に高い親和性を示します。ビーズ上にプロテインAを添加すると、粗血清、腹水または細胞培養上清からIgG画分を精製するために使用できる親和性樹脂が得られます。

Physical form

0.05%アジ化ナトリウムを含有する10 mM Tris-HCl、1 mM EDTA(pH 8.0)。

Legal Information

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

保管分類

12 - Non Combustible Liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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

Requirement of Smad3 and CREB-1 in mediating transforming growth factor-beta (TGF beta) induction of TGF beta 3 secretion.
Guangming Liu, Wei Ding, Jill Neiman, Kathleen M Mulder
The Journal of Biological Chemistry null
A note on penicillin resistance and beta-lactamase production in strains of Staphylococcus aureus recovered from different clinical materials in Nsukka, Nigeria.
Oguike, J U, et al.
The Journal of Communicable Diseases, 23, 200-201 (1991)
Mohammad Kamran et al.
Journal of immunology (Baltimore, Md. : 1950), 205(12), 3311-3318 (2020-11-15)
IL-13 plays a critical role in mediating many biological processes responsible for allergic inflammation. Mast cells express Il13 mRNA and produce IL-13 protein in response to antigenic stimulation. Enhancers are essential in promoting gene transcription and are thought to activate
Generation of p53 target database via integration of microarray and global p53 DNA-binding site analysis.
Suxing Liu, Asra Mirza, Luquan Wang
Methods in Molecular Biology null
Guodong Huang et al.
Autophagy, 12(8), 1292-1309 (2016-05-14)
Autophagy is a highly conserved intracellular degradation system, and recently was shown to display circadian rhythms in mice. The mechanisms underlying circadian regulation of autophagy, however, are still unclear. Here, we observed that numbers of autophagosomes and autolysosomes exhibit daily

関連コンテンツ

Protein and nucleic acid interaction reagents and resources for investing protein-RNA, protein-DNA, and protein-protein interactions and associated applications.

タンパク質-RNA、タンパク質-DNA、タンパク質-タンパク質相互作用の検討および関連するアプリケーションのためのタンパク質-核酸相互作用試薬およびリソース。

"Epigenetics describes heritable changes in gene expression caused by non-genetic mechanisms instead of by alterations in DNA sequence. These changes can be cell- or tissue-specific, and can be passed on to multiple generations. Epigenetic regulation enriches DNAbased information, allowing a cell to vary its response across diverse biological and environmental contexts. Although epigenetic mechanisms are primarily centered in the nucleus, these mechanisms can be induced by environmental signals such as hormones, nutrients, stress, and cellular damage, pointing to the involvement of cytoplasmic and extracellular factors in epigenetic regulation."

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).

グローバルトレードアイテム番号

カタログ番号GTIN
16-15704053252515330

ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.

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