生物来源
rabbit
质量水平
抗体形式
purified antibody
抗体产品类型
primary antibodies
克隆
15-10C-E4, monoclonal
种属反应性
human
制造商/商品名称
Upstate®
技术
ChIP: suitable (ChIP-seq)
ELISA: suitable
dot blot: suitable
inhibition assay: suitable (peptide)
multiplexing: suitable
western blot: suitable
同位素/亚型
IgG
NCBI登记号
UniProt登记号
运输
wet ice
靶向翻译后修饰
trimethylation (Lys4)
基因信息
human  ...  H3F3B(3021)   
一般描述
免疫原
应用
代表性批次数据。使用Magna ChIP HiSens试剂盒(目录号17-10460),3 µL 抗三甲基组蛋白H3(Lys4)抗体(目录号05-745R),20 µL蛋白A/G珠和1e6交联 HeLa细胞染色质进行染色质免疫沉淀,然后使用磁珠进行DNA纯化。使用标准规程从 Input 和 ChIP DNA 样品制备文库,带 Illumina 条形码适配器,并在 Illumina HiSeq 仪器上进行分析。在去除 TagDust(http://genome.gsc.riken.jp/osc/english/dataresource)标签后,使用 Bowtie(http://bowtie-bio.sourceforge.net/manual.shtml)映射了 FastQ 文件中的超过1800万次读取。使用 MACS(http://luelab.dfci.harvard.edu/MACS/)识别峰,并从 BigWig 和 BED 文件在 UCSC Genome Browser(http://genome.ucsc.edu)中以自定义轨道的形式显示峰和读数。在05-745R和07-473数据集中识别出的最高25%峰与HeLa S3的ENCODE H3K27Ac BROAD组蛋白轨迹中识别出的峰有99%重叠。
组蛋白
表观遗传学&核功能
生化/生理作用
外形
制备说明
处理建议:收到后,在取下瓶盖之前,将小瓶离心并轻轻混合溶液。分装到微量离心管中,并储存于 -20°C。避免反复冻融,其可能会破坏IgG并影响产品性能。注意:冷藏室温度变化至低于-20°C时可能导致-含甘油的溶液在储存过程中冻结。
分析说明
其他说明
法律信息
免责声明
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储存分类代码
12 - Non Combustible Liquids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
相关内容
Signaling Product Guide: Antibodies, small molecule inhibitors, kits, assays and proteins for signaling research.
"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).
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