H3K27ac(组蛋白H3赖氨酸27乙酰化)抗体符合EpiCypher的批次特异性SNAP-Certified™标准,在CUT&RUN和CUT&Tag应用中具有特异性和高效的靶标富集。这需要与相关组蛋白 PTMs (使用加标对照的 SNAP-CUTANA™ K-AcylStat Panel 测定,EpiCypher RD193002)的交叉反应性 <20%(图 1 和 图5)。在不同的细胞起始条件下,一致的基因组富集结果证实了高靶标效率:CUT&RUN中500k和50k的细胞量(图2-3),CUT&Tag中100k和10k的细胞量(图6-7)。即使在细胞数量减少的情况下,高效抗体也显示出相似的峰结构(图3和7)和高度保守的全基因组信号(图2和6)。H3K27ac与基因激活相关,并在活性增强子和启动子中富集[1]。
产品详情
产品名称:H3K27ac Antibody, SNAP-Certified™ for CUT&RUN and CUT&Tag/欣博盛生物
宿主来源:Rabbit
实验应用:CUT&RUN, CUT&Tag
免疫原:A synthetic peptide corresponding to histone H3 acetylated at lysine 27
克隆性:Monoclonal[2114-3E4]
保存温度:自收到之日起,4℃下可稳定储存1年。
验证数据
—— CUT&RUN
|
Figure 1: Average SNAP specificity analysis from two CUT&RUN experiments |
| CUT&RUN was performed as described in Figure 4. CUT&RUN sequencing reads were aligned to the unique DNA barcodes corresponding to each nucleosome in the K-AcylStat panel (x-axis). Data are expressed as a percent relative to on-target recovery (H3K27ac set to 100%). The antibody showed recovery of H3K27ac spike-in nucleosomes as well as H3K27ac nucleosomes that contain a proximal phosphorylation at S28 at both 500k and 50k cells. The antibody cross-reacts with extended acyl states (butyrylation and crotonylation) at H3K27, but these are typically low abundance in cells [2]. |
|
Figure 2: CUT&RUN genome-wide enrichment |
| CUT&RUN was performed as described in |
H3K27ac抗体在CUT&RUN和CUT&Tag中的特异性与高效富集研究

本文详细描述了一种H3K27ac抗体,该抗体符合EpiCypher批次特异性SNAP-Certified标准,适用于CUT&RUN和CUT&Tag方法。实验结果显示抗体在不同细胞起始条件下具有高靶标效率和一致性,证实了其在基因激活区域的富集特性。


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