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Bacterially Expressed sentence examples within bacterially expressed recombinant
Here, we prepared a subunit vaccine candidate derived from the bacterially expressed recombinant Fiber2 protein (termed as rFiber2 subunit vaccine) of FAdV-4 GZ-QL strain (a hypervirulent strain isolated in Guizhou province) and a recombinant plasmid pVAX1-Fiber2 as DNA vaccine candidate (termed as Fiber2 DNA vaccine).
Here, we prepared a subunit vaccine candidate derived from the bacterially expressed recombinant Fiber2 protein (termed as rFiber2 subunit vaccine) of FAdV-4 GZ-QL strain (a hypervirulent strain isolated in Guizhou province) and a recombinant plasmid pVAX1-Fiber2 as DNA vaccine candidate (termed as Fiber2 DNA vaccine).
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Finally, we used bacterially expressed recombinant α-SYN to generate amyloid fibrils and measure interactions with a pool of GFP-tagged potential partners.
Finally, we used bacterially expressed recombinant α-SYN to generate amyloid fibrils and measure interactions with a pool of GFP-tagged potential partners.
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Bacterially Expressed sentence examples within bacterially expressed protein
Direct binding of BPLF1 to the autophagy receptor SQSTM1/p62 (sequestosome 1) was confirmed by co-immunoprecipitation of transfected BPLF1 and by in vitro affinity isolation of bacterially expressed proteins.
Direct binding of BPLF1 to the autophagy receptor SQSTM1/p62 (sequestosome 1) was confirmed by co-immunoprecipitation of transfected BPLF1 and by in vitro affinity isolation of bacterially expressed proteins.
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Using purified, bacterially expressed proteins we demonstrate that the product of AN11127 accelerates nucleotide exchange on SarASAR1, but not on its closely related GTPase ArfAARF1, as expected for a bona fide GEF.
Using purified, bacterially expressed proteins we demonstrate that the product of AN11127 accelerates nucleotide exchange on SarASAR1, but not on its closely related GTPase ArfAARF1, as expected for a bona fide GEF.
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Bacterially Expressed sentence examples within bacterially expressed double
vigintioctopunctata was investigated using both in vitro synthesized and bacterially expressed double-stranded RNAs (dsRNAs) of HvvATPase A and HvvATPase E.
vigintioctopunctata was investigated using both in vitro synthesized and bacterially expressed double-stranded RNAs (dsRNAs) of HvvATPase A and HvvATPase E.
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Dietary delivery of bacterially expressed double-stranded RNA (dsRNA) has a great potential for management of Leptinotarsa decemlineata.
Dietary delivery of bacterially expressed double-stranded RNA (dsRNA) has a great potential for management of Leptinotarsa decemlineata.
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Bacterially Expressed sentence examples within bacterially expressed gst
To further consolidate the interaction between USP11 and BIP, we performed a GST pulldown assay with a bacterially expressed GST-tagged BIP.
To further consolidate the interaction between USP11 and BIP, we performed a GST pulldown assay with a bacterially expressed GST-tagged BIP.
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Bacterially expressed GST‐tagged Fibulin‐4 was shown to associate with baculovirus‐expressed His‐tagged VP55 in a dot‐blot overlay assay; moreover, baculovirus‐expressed His‐tagged VP55 was able to pull down GFP‐Fibulin‐4 expressed in the GCO cells.
Bacterially expressed GST‐tagged Fibulin‐4 was shown to associate with baculovirus‐expressed His‐tagged VP55 in a dot‐blot overlay assay; moreover, baculovirus‐expressed His‐tagged VP55 was able to pull down GFP‐Fibulin‐4 expressed in the GCO cells.
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Bacterially Expressed sentence examples within bacterially expressed dsrna
RESULTS
Feeding either the in vitro-synthesized or the bacterially expressed dsRNAs significantly impaired the normal physiology of H.
RESULTS
Feeding either the in vitro-synthesized or the bacterially expressed dsRNAs significantly impaired the normal physiology of H.
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vigintioctopunctata using dietary RNAi toxicity assays targeting eight HvCOPI subunits, including α-, β-, β′-, γ-, δ-, e-, ζ-, and Arf1-COPI using in vitro synthesized and bacterially expressed dsRNAs.
vigintioctopunctata using dietary RNAi toxicity assays targeting eight HvCOPI subunits, including α-, β-, β′-, γ-, δ-, e-, ζ-, and Arf1-COPI using in vitro synthesized and bacterially expressed dsRNAs.
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10.3389/fmicb.2021.757215
Recombinant IL-26 was bacterially expressed and studied for its microbicidal effects in culture.
Recombinant IL-26 was bacterially expressed and studied for its microbicidal effects in culture.
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10.1093/jb/mvab055
Respective SULT1C4 allozymes were bacterially expressed and purified by affinity chromatography.
Respective SULT1C4 allozymes were bacterially expressed and purified by affinity chromatography.
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10.3390/v13071230
In this study, we demonstrate that bacterially expressed, purified SHFL can decrease the efficiency of programmed ribosomal frameshifting in vitro at a variety of sites, including the RNA pseudoknot-dependent signals of the coronaviruses IBV, SARS-CoV and SARS-CoV-2, and the protein-dependent stimulators of the cardioviruses EMCV and TMEV.
In this study, we demonstrate that bacterially expressed, purified SHFL can decrease the efficiency of programmed ribosomal frameshifting in vitro at a variety of sites, including the RNA pseudoknot-dependent signals of the coronaviruses IBV, SARS-CoV and SARS-CoV-2, and the protein-dependent stimulators of the cardioviruses EMCV and TMEV.
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10.1101/2021.05.09.443341
To efficiently generate high-quality affinity reagents, synthetic nanobody co-binders and mono-binders with high affinity, specificity, and stability were selected by phage display screening of a vastly diverse, rationally randomized combinatorial library, bacterially expressed and site-specifically conjugated to gold nanoparticles (AuNPs) as multivalent in-solution sensors.
To efficiently generate high-quality affinity reagents, synthetic nanobody co-binders and mono-binders with high affinity, specificity, and stability were selected by phage display screening of a vastly diverse, rationally randomized combinatorial library, bacterially expressed and site-specifically conjugated to gold nanoparticles (AuNPs) as multivalent in-solution sensors.
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10.1016/j.neulet.2019.01.002
This was supported by biophysical measurements of bacterially expressed, recombinant protein.
This was supported by biophysical measurements of bacterially expressed, recombinant protein.
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10.1016/j.pharep.2018.12.001
Recombinant wild-type and SULT1A1 allozymes were bacterially expressed and affinity-purified.
Recombinant wild-type and SULT1A1 allozymes were bacterially expressed and affinity-purified.
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10.1016/j.antiviral.2019.02.013
This fusion protein, named CRM197(A)‐E2, was bacterially expressed and purified by chromatography.
This fusion protein, named CRM197(A)‐E2, was bacterially expressed and purified by chromatography.
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10.1111/1744-7917.12677
mosellana antenna‐specific OBP genes, SmosOBP11, 16 and 21, were cloned and bacterially expressed.
mosellana antenna‐specific OBP genes, SmosOBP11, 16 and 21, were cloned and bacterially expressed.
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10.1371/journal.pone.0215009
Bacterially expressed and purified Sfh1 was suggested to have the ability to transport fluorescently labeled PS between liposomes by fluorescence dequenching assay in vitro.
Bacterially expressed and purified Sfh1 was suggested to have the ability to transport fluorescently labeled PS between liposomes by fluorescence dequenching assay in vitro.
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