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  1. One-stop service, from design of gRNAs, preparing of single clones to sequencing analysis. Construct generation, Stable cell clones selection, Gene expression evaluation.

  2. CRISPR-Cas9 is a genome editing technology used to change parts of the genome. Learn how CRISPR-Cas9 works and discover its advantages and limitations.

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  3. Well-established technology platform & extensive experience in precision animal breeding. CRISPR Genome Editing service to improve animal production/welfare/disease resistance

  4. Synthesis of natural siRNA, miRNA and other small RNA or non-natural RNA. Inquire. Strict quality control to ensure the synthesis of high-quality Oligonucleotide.

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      • Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) gene-editing technology is the ideal tool of the future for treating diseases by permanently correcting deleterious base mutations or disrupting disease-causing genes with great precision and efficiency.
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  2. Jan 16, 2023 · Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) gene-editing technology is the ideal tool of the future for treating diseases by...

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  3. Oct 29, 2019 · CRISPR-Cas9 appears to be superseding ZFNs and TALENS as gene editing technology of choice for many scientists and has a high potential to trigger ground-breaking innovations not only in biology...

    • Sabina Semiz, Sabina Semiz, Philip C. Aka
    • 2019
  4. Mar 24, 2022 · Personalized or precision medicine combines genetic information with phenotypic and environmental characteristics to produce healthcare tailored to the individual and eliminates the constraints of “one-size-fits-all” therapy. Precision medicine is now possible thanks to cancer genome sequencing.

  5. Dec 2, 2019 · The use of CRISPR-cas9 to construct cell or animal models has greatly facilitated cancer research. CRISPR-cas9-based screening accelerates the identification of new drug targets and biomarkers, which will promote the discovery and development of precise cancer treatments.

    • Hui Xing, Ling-hua Meng
    • 10.1038/s41401-019-0322-9
    • 2020
    • Acta Pharmacol Sin. 2020 May; 41(5): 583-587.
  6. Dec 2, 2019 · In this review, we describe the progress of CRISPR-cas9-based unbiased screening in precision medicine including identification of new drug targets, biomarkers and elucidation of mechanisms...

    • Hui Xing, Ling-hua Meng
    • 2020
  7. Oct 15, 2023 · CRISPR/Cas9 nuclease achieves gene editing by a programmable single-guide RNA (sgRNA), which is a fusion of trans-activating RNA (tracrRNA) and CRISPR-targeting RNA (crRNA), to guide the Cas9 protein to the target DNA.

  8. Nov 8, 2023 · We will discuss CRISPR/Cas9-based diagnostics and therapeutic approaches. Finally, we will address future perspectives on CRISPR/Cas9 genome editing and the expansion of genome editors’ toolboxes with Cas9 orthologs, other CRISPR/Cas proteins, and recently described Fanzor enzymes.