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Jm109 de3 cells

Manufactured by Promega

JM109 (DE3) cells are a strain of Escherichia coli (E. coli) bacteria used for the expression of recombinant proteins. These cells are designed for high-level protein expression and are commonly used in molecular biology and biotechnology applications.

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2 protocols using jm109 de3 cells

1

Heterologous Expression and Purification of Ric-8A

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Rat GST-TEV-Ric-8A was expressed in Tni (Trichoplusia ni) cells infected with recombinant baculovirus (pFastBac, Invitrogen). Tni cells were obtained from Expression Systems, LLC. Rat GST-TEV-Ric-8A together with human Gαq were expressed in Tni (Trichuplusia ni) cells infected with two recombinant baculoviruses (pFastBac, Invitrogen). Human 6His-3C-Gαi1 WT or 6His-3C-Gαi1 ΔF354 were expressed in Rosetta 2(DE3) cells (Merck Millipore). Human Gαi1 (6His between M119 and T120) was expressed in JM109 (DE3) cells (Promega). MBP-Ric-8A (423–530) was expressed in Rosetta 2 (DE3) cells. The HEK293T cell line (CRL-11268) was obtained from the American Type Culture Collection (ATCC). Crispr/Cas9 procedures were used previously to delete RIC-8A in the HEK293T cells (Papasergi-Scott et al., 2018 (link)). 3X-FLAG-Ric-8A point mutant plasmids were transfected and selected for stable expression with Hygromycin B.
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2

Heterologous Expression and Purification of Ric-8A

Check if the same lab product or an alternative is used in the 5 most similar protocols
Rat GST-TEV-Ric-8A was expressed in Tni (Trichoplusia ni) cells infected with recombinant baculovirus (pFastBac, Invitrogen). Tni cells were obtained from Expression Systems, LLC. Rat GST-TEV-Ric-8A together with human Gαq were expressed in Tni (Trichuplusia ni) cells infected with two recombinant baculoviruses (pFastBac, Invitrogen). Human 6His-3C-Gαi1 WT or 6His-3C-Gαi1 ΔF354 were expressed in Rosetta 2(DE3) cells (Merck Millipore). Human Gαi1 (6His between M119 and T120) was expressed in JM109 (DE3) cells (Promega). MBP-Ric-8A (423–530) was expressed in Rosetta 2 (DE3) cells. The HEK293T cell line (CRL-11268) was obtained from the American Type Culture Collection (ATCC). Crispr/Cas9 procedures were used previously to delete RIC-8A in the HEK293T cells (Papasergi-Scott et al., 2018 (link)). 3X-FLAG-Ric-8A point mutant plasmids were transfected and selected for stable expression with Hygromycin B.
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