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Mackenzie Scott on Muck Rack

Mackenzie Scott

Inuvik
As seen in: Medium, MSN Canada, Bloomberg News, Forbes, Canadian Broadcasting Corporation (CBC), CBLT-TV (Toronto, ON), CBQG-AM (Wrigley, NT), CBUA-FM (Atlin, BC), CFYK-TV (Yellowknife, NT), KCBS-TV (Los Angeles, CA) and
Former Videojournalist for CBC in Inuvik, NWT. Former Reporter @KBJR6news. ASU Graduate and a part of Cronkite Nation. Born and raised in Edmonton.
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Articles

Futures and Commodity Market News

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By Mackenzie Scott
| futures.tradingcharts.com
Jun 22, 2026 (The Australian - ABIX via COMTEX) -- The Queensland Critical Minerals Fund will be allocated $100m in today's state budget. Resources Minister Dale Last says Queensland can become a global leader in critical minerals, and this investment will send a clear message that the state is "open for business".
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Membrane Biology: Two binding sites are better than one

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By Mackenzie Scott, John Burke
| eLife
Thousands of chemical reactions take place in cells every second, and many of them must take place at the correct location on a specific intracellular membrane. An enzyme called VPS34, also known as class III PI3K, has a crucial role in this process, as does a family of proteins known as Rab GTPases. VPS34 is conserved in all eukaryotes, regulating core “housekeeping” signalling pathways, such as autophagy and endosomal trafficking.
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Molecular basis for plasma membrane recruitment of PI4KA by EFR3

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By Sushant Suresh, Alexandria L. Shaw, Joshua G Pemberton, Mackenzie Scott, Noah Harris, Matthew A. H. Parson, Meredith L. Jenkins, Pooja Rohilla, Alejandro Alvarez-Prats, Tamas Balla, Calvin Yip, John Burke
| Science Magazine Verified
MATERIALS AND METHODS Plasmids containing genes for full-length PI4KA, TTC7B, and FAM126A (1 to 308) were cloned into the MultiBac vector, pACEBac1 (Geneva Biotech) as described in (21). Plasmid encoding TTC7B and FAM126A (1 to 308) was subcloned into a pOPT vector containing an N-terminal 10× histidine tag, followed by a 2× Strep tag, followed by a tobacco etch virus (TEV) protease cleavage site. On the basis of the evolutionary conservation of the C-terminal tail of EFR3A (fig.
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