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相关概念视频

In-vitro Mutagenesis01:16

In-vitro Mutagenesis

13.9K
To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.
13.9K
CRISPR01:59

CRISPR

49.8K
Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced...
49.8K
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

5.9K
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
5.9K
Base Excision Repair01:54

Base Excision Repair

22.2K
One of the common DNA damages is the chemical alteration of single bases by alkylation, oxidation, or deamination. The altered bases cause mispairing and strand breakage during replication. This type of damage causes minimal change to the DNA double helix structure and can be repaired by the base excision repair (BER) pathways. BER corrects damaged DNA sequences by removing the damaged base and restoring the original base sequence using the complementary strand as a template.
The first step of...
22.2K
Next-generation Sequencing03:00

Next-generation Sequencing

88.4K
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
88.4K
Genome Copying Errors02:46

Genome Copying Errors

4.2K
DNA replication is a well-evolved process that copies millions of base pairs with high fidelity during each cell division. Occasionally a wrong base or a long stretch of wrong bases may get added to the daughter strands. If the errors are left unchecked, cells might accumulate several mutations that might endanger their  survival. Therefore, the copying errors are checked and repaired at three levels.
4.2K

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相关实验视频

Updated: Jun 12, 2025

Genetic Manipulation in &Delta;ku80 Strains for Functional Genomic Analysis of Toxoplasma gondii
09:52

Genetic Manipulation in Δku80 Strains for Functional Genomic Analysis of Toxoplasma gondii

Published on: July 12, 2013

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编程的DNA消除程序.

Kazufumi Mochizuki1

  • 1Institute of Human Genetics (IGH), CNRS and University of Montpellier, Montpellier, France.

Current biology : CB
|September 24, 2024
PubMed
概括

大多数细胞共享相同的基因组,但脊椎动物中发育的血细胞是例外. V(D) J重组混合淋巴细胞中的基因段,为T细胞受体和免疫球蛋白创造多种抗原结合区域.

科学领域:

  • 免疫学 免疫学 免疫学
  • 遗传学 遗传学 是一个
  • 发展生物学 发展生物学

背景情况:

  • 多细胞生物通常在体细胞中保持相同的基因组.
  • 这种基因组统一性使体细胞重编程和克隆等过程成为可能.
  • 在脊椎动物的免疫系统中有一个例外,特别是在发育中的淋巴细胞中.

研究的目的:

  • 为了突显脊椎动物血细胞中一个体-一个基因组原则的例外.
  • 在淋巴细胞发育中引入V(D) J重组的过程.

主要方法:

  • 审查已确立的细胞身份的生物原则.
  • 描述V(D) J重组作为一个独特的遗传机制.

主要成果:

  • 脊椎动物的淋巴细胞表现出其他体细胞中无法发现的基因组多样性.
  • V(D) J重组是导致这种基因组变异的机制.

结论:

  • 在一个个体的细胞中具有相同基因组的原则并不普遍适用.
  • 淋巴细胞中的J重组是适应性免疫的关键过程.

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Electroporation-Based CRISPR-Cas9-Mediated Gene Knockout in THP-1 Cells and Single-Cell Clone Isolation
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相关实验视频

Last Updated: Jun 12, 2025

Genetic Manipulation in &Delta;ku80 Strains for Functional Genomic Analysis of Toxoplasma gondii
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Genetic Manipulation in Δku80 Strains for Functional Genomic Analysis of Toxoplasma gondii

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Electroporation-Based CRISPR-Cas9-Mediated Gene Knockout in THP-1 Cells and Single-Cell Clone Isolation
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