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  2. MagSafe (wireless charger) - Wikipedia

    en.wikipedia.org/wiki/MagSafe_(wireless_charger)

    The first version of the MagSafe Charger, released in 2020, delivers up to 15 W of power to iPhones 12, 12 Pro, and newer, with the exception of iPhone 12 Mini and 13 Mini, which support 12 W. [12] The Wall Street Journal found the MagSafe Charger charged at half the speed of a 20 W wired charger. [13]

  3. Cas12a - Wikipedia

    en.wikipedia.org/wiki/Cas12a

    Like other Cas enzymes, Cas12a binds to a "guide" RNA (termed a crRNA, or CRISPR RNA) which targets it to a DNA sequence in a specific and programmable matter. In the host organism, the crRNA contains a constant region that is recognized by the Cas12a protein and a "spacer" region that is complementary to a piece of foreign nucleic acid (e.g. a ...

  4. CRISPR activation - Wikipedia

    en.wikipedia.org/wiki/CRISPR_activation

    See: Guide RNA, CRISPR. Complementary base pairing between the sgRNA and genomic DNA allows targeting of Cas9 or dCas9. A small guide RNA (sgRNA), or gRNA is an RNA with around 20 nucleotides used to direct Cas9 or dCas9 to their targets. gRNAs contain two major regions of importance for CRISPR systems: the scaffold and spacer regions.

  5. MagSafe - Wikipedia

    en.wikipedia.org/wiki/MagSafe

    The MagSafe connector returned in 2021 as "MagSafe 3" with the introduction of updated 14-inch and 16-inch MacBook Pro models. [9] Apple also uses the MagSafe name for a wireless power transfer and accessory-attachment standard for the iPhone based on the Qi standard, introduced with the iPhone 12 and 12 Pro. [10]

  6. Here’s what a Nobel Prize-winning scientist wants you ... - AOL

    www.aol.com/nobel-prize-winning-scientist-breaks...

    In his new book “The Catalyst,” Thomas R. Cech talks about the Covid-19 vaccines, what RNA means for future health crises and how gene editing with CRISPR factors in.

  7. CRISPR interference - Wikipedia

    en.wikipedia.org/wiki/CRISPR_interference

    CRISPR interference (CRISPRi) is a genetic perturbation technique that allows for sequence-specific repression of gene expression in prokaryotic and eukaryotic cells. [1] It was first developed by Stanley Qi and colleagues in the laboratories of Wendell Lim , Adam Arkin, Jonathan Weissman , and Jennifer Doudna . [ 2 ]

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