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相关概念视频

Ribosome Profiling02:24

Ribosome Profiling

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Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique...
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Phase II Reactions: Methylation Reactions01:17

Phase II Reactions: Methylation Reactions

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Methylation is a phase II biotransformation process involving the attachment of a methyl group to a substrate. Enzymes known as methyltransferases orchestrate this reaction.
The mechanism of methylation unfolds in two stages. The first stage sees a methyltransferase enzyme facilitating the transfer of a methyl group from S-adenosylmethionine (SAM) to the substrate, forming S-adenosylhomocysteine (SAH). The second stage involves further metabolism of SAH into homocysteine, which can be recycled...
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DNA Topoisomerases02:02

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Topoisomerases are enzymes that relax overwound DNA molecules during various cell processes, including DNA replication and transcription. These enzymes regulate positive and negative DNA supercoiling without changing the nucleotide sequence. DNA overwinding in a clockwise direction results in positively supercoiled DNA, whereas underwinding in a counterclockwise direction produces negatively supercoiled DNA.
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DNA unwinding helicase enzymes are a type of motor protein. Motor proteins can translocate along filaments or polymers using energy generated from ATP hydrolysis. Helicases are involved in all the important cellular processes where DNA unwinding is required, such as DNA replication, repair, recombination, and transcription. They are present in all living organisms, but vary in their structure, function, and mechanism of action. For example, in prokaryotes, DnaB helicase binds and translocates...
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DNA replication involves the separation of the two strands of the double helix, with each strand serving as a template from which the new complementary strand is copied.  After replication, each double-stranded DNA includes one parental or “old” strand and one “new” strand. This is known as semiconservative replication. The resulting DNA molecules have the same sequence and are divided equally into the two daughter cells.
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相关实验视频

Updated: Feb 4, 2026

Laser Capture Microdissection of Mammalian Tissue
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激光捕获微解剖,随后进行DNA甲基化剖析.

Lu Liu1, Yingchuo Hu2,3,4, Chunhong Zheng5

  • 1Changping Laboratory, Beijing, China. luliu@cpl.ac.cn.

Methods in molecular biology (Clifton, N.J.)
|February 2, 2026
PubMed
概括

我们将激光捕获微解剖与酶性甲基-seq (EM-seq) 结合起来,分析罕见细胞中的DNA甲基化. 这种方法提供高质量的表观遗传数据,仅从100个细胞获得,用于生物标志物发现和个性化医学.

关键词:
没有二硫酸盐的转换.基因组甲基化概况的DNA甲基化分析酶性甲基-seqq 的使用.低输入的图书馆准备工作.空间分辨的甲基化分析

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相关实验视频

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16:34

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科学领域:

  • 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
  • 分子生物学分子生物学
  • 基因组学就是基因组学.

背景情况:

  • 组织异质性混了DNA甲基化分析.
  • 激光捕获微解剖 (LCM) 隔离了特定的细胞群,但产生了较低的DNA.
  • 传统的双硫酸盐测序需要大量的DNA输入,并导致降解.

研究的目的:

  • 开发一种低输入的DNA甲基化分析方法,用于LCM分离的细胞.
  • 将LCM与无二硫酸盐酶转化技术集成在一起.
  • 为了能够对罕见细胞群体进行强有力的表观遗传分析.

主要方法:

  • 激光捕捉微解剖 (LCM) 与酶性甲基-seq (EM-seq) 的整合.
  • 优化用于酶性DNA转换的低输入库准备协议.
  • 无二硫酸盐甲基化概况,以保持DNA完整性和减少GC偏差.

主要成果:

  • 从仅100个细胞中实现了强大的和可重复的甲基化概况.
  • 获得的数据质量与大量组织样本相比较.
  • 证明了分离瘤细胞用于生物标志物发现的实用性.

结论:

  • LCM-EM-seq是一个可扩展的框架,用于空间解析的表观遗传分析.
  • 能够对罕见细胞群的甲基化意识研究.
  • 提升生物标志物发现,向疗法和个性化表观遗传特征.