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相关概念视频

Buffers02:56

Buffers

173.1K
A solution containing appreciable amounts of a weak conjugate acid-base pair is called a buffer solution, or a buffer. Buffer solutions resist a change in pH when small amounts of a strong acid or a strong base are added. A solution of acetic acid and sodium acetate is an example of a buffer that consists of a weak acid and its salt: CH3COOH (aq) + CH3COONa (aq). An example of a buffer that consists of a weak base and its salt is a solution of ammonia and ammonium chloride: NH3 (aq) + NH4Cl...
173.1K
Lagging Strand Synthesis01:59

Lagging Strand Synthesis

61.4K
During replication, the complementary strands in double-stranded DNA are synthesized at different rates. Replication first begins on the leading strand. Replication starts later, occurs more slowly, and proceeds discontinuously on the lagging strand.
There are several major differences between synthesis of the leading strand and synthesis of the lagging strand. 1) Leading strand synthesis happens in the direction of replication fork opening, whereas lagging strand synthesis happens in the...
61.4K
Single-Strand DNA Binding Proteins01:03

Single-Strand DNA Binding Proteins

16.7K
For successful DNA replication, the unwinding of double-stranded DNA must be accompanied by stabilization and protection of the separated single strands of the DNA. This crucial task is performed by single-strand DNA-binding (SSB) proteins. They bind to the DNA in a sequence-independent manner, which means that the nitrogenous bases of the DNA need not be present in a specific order for binding of SSB proteins to it. The binding of SSB proteins straightens single-stranded DNA (ssDNA) and makes...
16.7K
Buffers: Buffer Capacity01:09

Buffers: Buffer Capacity

2.5K
Buffer capacity is the quantitative measure of a buffer to resist the change in pH. As shown in the following equation, the buffer capacity, denoted by 'beta', is expressed as the number of moles of acid or base needed to change the pH of a one-liter buffer solution by 1 unit. Here, Ca and Cb indicate the number of moles of acid and base, respectively. Note that dpH represents the change in pH.
In the graph, pH is plotted as a function of the number of moles of base (Cb) added to a weak...
2.5K
Fixing Double-strand Breaks02:04

Fixing Double-strand Breaks

14.8K
The double-stranded structure of DNA has two major advantages. First, it serves as a safe repository of genetic information where one strand serves as the back-up in case the other strand is damaged. Second, the double-helical structure can be wrapped around proteins called histones to form nucleosomes, which can then be tightly wound to form chromosomes. This way, DNA chains up to 2 inches long can be contained within microscopic structures in a cell. A double-stranded break not only damages...
14.8K
Buffer Effectiveness02:19

Buffer Effectiveness

55.4K
Buffer solutions do not have an unlimited capacity to keep the pH relatively constant . Instead, the ability of a buffer solution to resist changes in pH relies on the presence of appreciable amounts of its conjugate weak acid-base pair. When enough strong acid or base is added to substantially lower the concentration of either member of the buffer pair, the buffering action within the solution is compromised.
The buffer capacity is the amount of acid or base that can be added to a given volume...
55.4K

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Separation of Single-stranded DNA, Double-stranded DNA and RNA from an Environmental Viral Community Using Hydroxyapatite Chromatography
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DNA 链缓冲器

Dominic Scalise, Nisita Dutta, Rebecca Schulman

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    此摘要是机器生成的。

    研究人员开发了新的寡核酸缓冲器,以精确控制DNA度,使基于DNA的系统能够稳定可靠地运行. 这些缓冲器提供可调节的设置点,抗扰性和快速响应时间.

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    科学领域:

    • 生物化学
    • 化学工程
    • 分子生物学

    背景情况:

    • 传统的缓冲系统主要调节离子度,如 (pH).
    • 现有的缓冲机制在控制复杂分子,如DNA序列方面是有限的.

    研究的目的:

    • 引入一种能够调节短DNA序列 (寡核酸) 的新类缓冲剂.
    • 为设计和调整寡核酸缓冲器提供数学框架.

    主要方法:

    • 开发用于选择速率常数以控制缓冲器属性 (设置点,容量,响应时间) 的数学公式.
    • 设计特定的DNA序列和度以达到所需的速率常数.
    • 在不同条件下保持稳定度的寡核酸缓冲体的实验证明.

    主要成果:

    • 尽管有50至500nM的干扰,但寡核酸缓冲器成功保持了10至80nM的设定点度.
    • 这些缓冲器的响应时间从10分钟到1.5小时不等.
    • 证明了多个缓冲器的并行操作,没有交叉干扰.

    结论:

    • 在合成生物学和自组合中,寡核酸缓冲提供了稳定DNA度的强大方法.
    • 这些缓冲器可以提高基于DNA的分子系统的可靠性和持续时间.
    • 缓冲原理有可能扩展到DNA以外的其他分子物种.