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Typically, one or more subcultures of cells can be made for analysis and selection of the correctly modified cells.

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Thanks, we are happy it helped better explain knockout mice for you!☺

"They" are the $50 billion a year association who are raking in all that money!

But the project had promising results, as he said its a potential cure, not a suggestion

CRISPR/Cas9 and Cre/LoxP recombination are two distinct genetic engineering tools that serve different purposes in the generation of knockout mice, and they can be used in conjunction for specific applications. While both techniques can be used to create knockout mice, they are not redundant, and their combined use can provide certain advantages. 1. CRISPR/Cas9 for Gene Targeting: Introduction of Mutations: CRISPR/Cas9 technology is commonly used to introduce specific mutations in a target gene. It involves designing a guide RNA (gRNA) that guides the Cas9 enzyme to a specific DNA sequence, where it induces double-strand breaks (DSBs). These DSBs can lead to insertions or deletions (indels) during the repair process, resulting in gene disruption or knockout. 2. Cre/LoxP Recombination: Conditional Knockouts: Cre/LoxP recombination is a tool used to achieve conditional gene knockout. It involves the use of two key elements: Cre recombinase enzyme and LoxP recognition sites. LoxP sites are inserted flanking a gene of interest, and Cre recombinase catalyzes recombination between these sites. This process can lead to the excision of the floxed gene, effectively knocking it out in a tissue-specific or inducible manner. Using both CRISPR/Cas9 and Cre/LoxP recombination together can offer the following advantages: 1. Precise Targeting: CRISPR/Cas9 allows for precise modification of a specific gene at its endogenous locus, ensuring that the mutation is introduced exactly where it's needed. 2. Flexibility: Cre/LoxP recombination enables conditional knockout strategies, allowing researchers to control when and where a gene is disrupted. This is particularly useful for studying genes with essential functions at different stages of development or in specific tissues. 3. Tissue-Specific Knockouts: By combining CRISPR/Cas9 and Cre/LoxP, researchers can create knockout mice with tissue-specific gene disruption. CRISPR/Cas9 is used to introduce LoxP sites or other modifications to the target gene, and Cre recombinase is subsequently expressed under the control of a tissue-specific promoter. 4. Temporal Control: Cre/LoxP allows for temporal control of gene knockout, whereas CRISPR/Cas9 disrupts the gene permanently. This temporal control can be critical for studying genes with complex functions that change over time. In summary, while both CRISPR/Cas9 and Cre/LoxP recombination can be used to create knockout mice, they serve complementary roles. CRISPR/Cas9 is primarily used for precise gene editing, while Cre/LoxP recombination offers conditional and tissue-specific knockout capabilities. Combining these techniques allows researchers to achieve more sophisticated and flexible control over gene knockout experiments, making it a valuable strategy in mouse genetics research.

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Thanks for your interest in our knockout mice. More information could be found at: www.cyagen.com/us/en/service/crispr-based-genome-editing-knockout-mice.html