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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
4℃
- 保质期:
1年
- 英文名:
3x BRD Homogeneous Assay Buffer 1
- 库存:
100
- 供应商:
艾美捷科技
- CAS号:
无
3x BRD 均质检测缓冲液 1,3x BRD Homogeneous Assay Buffer 1 ,3x BRD 均质检测缓冲液 1,3x BRD Homogeneous Assay Buffer 1
3x BRD 均质检测缓冲液 1-3x BRD Homogeneous Assay Buffer 1
产品货号:BPS-33001
产品规格:10ml

该3x BRD 均质检测缓冲液 1的背景资料请参阅该产品的英文datasheet。

3x BRD 均质检测缓冲液 1,3x BRD Homogeneous Assay Buffer 1
Bromodomain/Assay Kit

3x BRD 均质检测缓冲液 1-3x BRD Homogeneous Assay Buffer 1 该3x BRD 均质检测缓冲液 1的保存建议请参阅该产品的英文datasheet。
点击:3x BRD 均质检测缓冲液 1-3x BRD Homogeneous Assay Buffer 1 更多BPS biosciencer产品信息欢迎联系我们

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Therapeutic Potential of Dimethyl Fumarate for the Treatment of High-Fat/High-Sucrose Diet-Induced Obesity.
Inhibitors of malaria parasite cyclic nucleotide phosphodiesterases block asexual blood-stage development and mosquito transmission
Analysis of RB Action in DNA Damage Checkpoint Response
checkpoint response: (1) transcriptional repression of E2F-regulated genes (cyclin A reporter assay); (2) induction of cell cycle arrest (Brd-U incorporation assay); and (3) inhibition of DNA double-strand break accumulation (phosphorylated-histone H2A.X
RNase Protection Assay--RNA酶保护试验
RNA酶保护试验(RNase Protection Assay,RPA)是通过液相杂交的方式,用反义RNA探针与样品杂交,以检测RNA表达的技术。与Northern杂交和RT-PCR比较,RPA有以下几个优点:1. 检测灵敏度比Northern杂交高。由于Northern杂交步骤中转膜和洗膜都将造成样品和探针的损失,使灵敏度下降,而RPA将所有杂交体系进行电泳,故损失小,提高了灵敏度。2. 由于PCR扩增过程中效率不均一和反应“平台”问题,基于PCR产物量进行分析所得数据的可靠性将下降
RNA酶保护试验((RNase Protection Assay,RPA)方法
,再加入3M NaAc 10μl、预冷无水乙醇250μl,混匀后,-20OC静置30min。4OC离心13500g×10min。弃上清液,沉淀用75%乙醇100μl洗涤,4OC离心13500g×2min, 弃上清液。室温下挥发残留乙醇。加入50μl杂交缓冲液溶解沉淀,4OC下保存待用。可用尿素-聚丙烯酰胺凝胶电泳检测探针质量。(参见本节电泳步骤)。 2.杂交 (1) RNA提取后溶解在杂交缓冲液中,浓度为1μg/μl。 (2)取8μl RNA加入1-3μl探针(根据探针检测
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