cercopithecus aethiops Search Results


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Coriell Institute for Medical Research african green monkey fibroblast
(A) Summary of mRNA splice variants made by individuals with the A or G variant at exon 6 splice acceptor site (rs10774671). Individuals with the A allele have lowered OAS activity (see text). (B) Tenfold serial dilutions of yeast expressing human RNase L and the indicated human OAS1 isoform imaged after 48 hours of growth on galactose medium. (C) Immunoblot analysis of OAS1, RNase L and Us11 expression from yeast (D) OAS1 Immunoblot of human cell lines A549 and a primary Human <t>Fibroblast</t> (HF) with or without IFN-α stimulation. Isoform lane is a mixture of 293T cell lysates transfected with pcDNA6 expression vector encoding human OAS1 p42 or p46 (top) Sanger sequencing traces at the OAS1 exon 6 splice junction for each cell lines are shown (bottom) (E) Gel image of ATP polymerization assay. Indicated human OAS1 isoforms were expressed and purified from E. coli as MBP fusion proteins and incubated with poly I:C and [ɑ−32P] ATP for 2h before resolving by polyacrylamide gel electrophoresis (methods). Lane 1–4 are derived from reactions containing 5, 1, 0.2, or 0.04 μM OAS1, respectively. All data are representative of at least two independent experiments.
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Marburg GmbH marmosets cercopithecus aethiops
(A) Summary of mRNA splice variants made by individuals with the A or G variant at exon 6 splice acceptor site (rs10774671). Individuals with the A allele have lowered OAS activity (see text). (B) Tenfold serial dilutions of yeast expressing human RNase L and the indicated human OAS1 isoform imaged after 48 hours of growth on galactose medium. (C) Immunoblot analysis of OAS1, RNase L and Us11 expression from yeast (D) OAS1 Immunoblot of human cell lines A549 and a primary Human <t>Fibroblast</t> (HF) with or without IFN-α stimulation. Isoform lane is a mixture of 293T cell lysates transfected with pcDNA6 expression vector encoding human OAS1 p42 or p46 (top) Sanger sequencing traces at the OAS1 exon 6 splice junction for each cell lines are shown (bottom) (E) Gel image of ATP polymerization assay. Indicated human OAS1 isoforms were expressed and purified from E. coli as MBP fusion proteins and incubated with poly I:C and [ɑ−32P] ATP for 2h before resolving by polyacrylamide gel electrophoresis (methods). Lane 1–4 are derived from reactions containing 5, 1, 0.2, or 0.04 μM OAS1, respectively. All data are representative of at least two independent experiments.
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Cerco Inc pithecus aethiops tantalus
(A) Summary of mRNA splice variants made by individuals with the A or G variant at exon 6 splice acceptor site (rs10774671). Individuals with the A allele have lowered OAS activity (see text). (B) Tenfold serial dilutions of yeast expressing human RNase L and the indicated human OAS1 isoform imaged after 48 hours of growth on galactose medium. (C) Immunoblot analysis of OAS1, RNase L and Us11 expression from yeast (D) OAS1 Immunoblot of human cell lines A549 and a primary Human <t>Fibroblast</t> (HF) with or without IFN-α stimulation. Isoform lane is a mixture of 293T cell lysates transfected with pcDNA6 expression vector encoding human OAS1 p42 or p46 (top) Sanger sequencing traces at the OAS1 exon 6 splice junction for each cell lines are shown (bottom) (E) Gel image of ATP polymerization assay. Indicated human OAS1 isoforms were expressed and purified from E. coli as MBP fusion proteins and incubated with poly I:C and [ɑ−32P] ATP for 2h before resolving by polyacrylamide gel electrophoresis (methods). Lane 1–4 are derived from reactions containing 5, 1, 0.2, or 0.04 μM OAS1, respectively. All data are representative of at least two independent experiments.
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Stouffer Industries evaluation of vervets (cercopithecus aethiops) as a potential research model for assisted reproductive
(A) Summary of mRNA splice variants made by individuals with the A or G variant at exon 6 splice acceptor site (rs10774671). Individuals with the A allele have lowered OAS activity (see text). (B) Tenfold serial dilutions of yeast expressing human RNase L and the indicated human OAS1 isoform imaged after 48 hours of growth on galactose medium. (C) Immunoblot analysis of OAS1, RNase L and Us11 expression from yeast (D) OAS1 Immunoblot of human cell lines A549 and a primary Human <t>Fibroblast</t> (HF) with or without IFN-α stimulation. Isoform lane is a mixture of 293T cell lysates transfected with pcDNA6 expression vector encoding human OAS1 p42 or p46 (top) Sanger sequencing traces at the OAS1 exon 6 splice junction for each cell lines are shown (bottom) (E) Gel image of ATP polymerization assay. Indicated human OAS1 isoforms were expressed and purified from E. coli as MBP fusion proteins and incubated with poly I:C and [ɑ−32P] ATP for 2h before resolving by polyacrylamide gel electrophoresis (methods). Lane 1–4 are derived from reactions containing 5, 1, 0.2, or 0.04 μM OAS1, respectively. All data are representative of at least two independent experiments.
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AddexBio Inc cos-7
(A) Summary of mRNA splice variants made by individuals with the A or G variant at exon 6 splice acceptor site (rs10774671). Individuals with the A allele have lowered OAS activity (see text). (B) Tenfold serial dilutions of yeast expressing human RNase L and the indicated human OAS1 isoform imaged after 48 hours of growth on galactose medium. (C) Immunoblot analysis of OAS1, RNase L and Us11 expression from yeast (D) OAS1 Immunoblot of human cell lines A549 and a primary Human <t>Fibroblast</t> (HF) with or without IFN-α stimulation. Isoform lane is a mixture of 293T cell lysates transfected with pcDNA6 expression vector encoding human OAS1 p42 or p46 (top) Sanger sequencing traces at the OAS1 exon 6 splice junction for each cell lines are shown (bottom) (E) Gel image of ATP polymerization assay. Indicated human OAS1 isoforms were expressed and purified from E. coli as MBP fusion proteins and incubated with poly I:C and [ɑ−32P] ATP for 2h before resolving by polyacrylamide gel electrophoresis (methods). Lane 1–4 are derived from reactions containing 5, 1, 0.2, or 0.04 μM OAS1, respectively. All data are representative of at least two independent experiments.
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Coriell Institute for Medical Research african green monkey fibroblasts (cercopithecus aethiops
(A) Summary of mRNA splice variants made by individuals with the A or G variant at exon 6 splice acceptor site (rs10774671). Individuals with the A allele have lowered OAS activity (see text). (B) Tenfold serial dilutions of yeast expressing human RNase L and the indicated human OAS1 isoform imaged after 48 hours of growth on galactose medium. (C) Immunoblot analysis of OAS1, RNase L and Us11 expression from yeast (D) OAS1 Immunoblot of human cell lines A549 and a primary Human <t>Fibroblast</t> (HF) with or without IFN-α stimulation. Isoform lane is a mixture of 293T cell lysates transfected with pcDNA6 expression vector encoding human OAS1 p42 or p46 (top) Sanger sequencing traces at the OAS1 exon 6 splice junction for each cell lines are shown (bottom) (E) Gel image of ATP polymerization assay. Indicated human OAS1 isoforms were expressed and purified from E. coli as MBP fusion proteins and incubated with poly I:C and [ɑ−32P] ATP for 2h before resolving by polyacrylamide gel electrophoresis (methods). Lane 1–4 are derived from reactions containing 5, 1, 0.2, or 0.04 μM OAS1, respectively. All data are representative of at least two independent experiments.
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Cerco Inc diet and feeding behaviour of cercopithecus aethiops tantalus
(A) Summary of mRNA splice variants made by individuals with the A or G variant at exon 6 splice acceptor site (rs10774671). Individuals with the A allele have lowered OAS activity (see text). (B) Tenfold serial dilutions of yeast expressing human RNase L and the indicated human OAS1 isoform imaged after 48 hours of growth on galactose medium. (C) Immunoblot analysis of OAS1, RNase L and Us11 expression from yeast (D) OAS1 Immunoblot of human cell lines A549 and a primary Human <t>Fibroblast</t> (HF) with or without IFN-α stimulation. Isoform lane is a mixture of 293T cell lysates transfected with pcDNA6 expression vector encoding human OAS1 p42 or p46 (top) Sanger sequencing traces at the OAS1 exon 6 splice junction for each cell lines are shown (bottom) (E) Gel image of ATP polymerization assay. Indicated human OAS1 isoforms were expressed and purified from E. coli as MBP fusion proteins and incubated with poly I:C and [ɑ−32P] ATP for 2h before resolving by polyacrylamide gel electrophoresis (methods). Lane 1–4 are derived from reactions containing 5, 1, 0.2, or 0.04 μM OAS1, respectively. All data are representative of at least two independent experiments.
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European Directorate for the Quality of Medicines and HealthCare leuprorelin human insulin
(A) Summary of mRNA splice variants made by individuals with the A or G variant at exon 6 splice acceptor site (rs10774671). Individuals with the A allele have lowered OAS activity (see text). (B) Tenfold serial dilutions of yeast expressing human RNase L and the indicated human OAS1 isoform imaged after 48 hours of growth on galactose medium. (C) Immunoblot analysis of OAS1, RNase L and Us11 expression from yeast (D) OAS1 Immunoblot of human cell lines A549 and a primary Human <t>Fibroblast</t> (HF) with or without IFN-α stimulation. Isoform lane is a mixture of 293T cell lysates transfected with pcDNA6 expression vector encoding human OAS1 p42 or p46 (top) Sanger sequencing traces at the OAS1 exon 6 splice junction for each cell lines are shown (bottom) (E) Gel image of ATP polymerization assay. Indicated human OAS1 isoforms were expressed and purified from E. coli as MBP fusion proteins and incubated with poly I:C and [ɑ−32P] ATP for 2h before resolving by polyacrylamide gel electrophoresis (methods). Lane 1–4 are derived from reactions containing 5, 1, 0.2, or 0.04 μM OAS1, respectively. All data are representative of at least two independent experiments.
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Marburg GmbH experimentelle infektionen von cercopithecus aethiops mit dem erreger des frankfurt.marburg.syndroms (fms)
(A) Summary of mRNA splice variants made by individuals with the A or G variant at exon 6 splice acceptor site (rs10774671). Individuals with the A allele have lowered OAS activity (see text). (B) Tenfold serial dilutions of yeast expressing human RNase L and the indicated human OAS1 isoform imaged after 48 hours of growth on galactose medium. (C) Immunoblot analysis of OAS1, RNase L and Us11 expression from yeast (D) OAS1 Immunoblot of human cell lines A549 and a primary Human <t>Fibroblast</t> (HF) with or without IFN-α stimulation. Isoform lane is a mixture of 293T cell lysates transfected with pcDNA6 expression vector encoding human OAS1 p42 or p46 (top) Sanger sequencing traces at the OAS1 exon 6 splice junction for each cell lines are shown (bottom) (E) Gel image of ATP polymerization assay. Indicated human OAS1 isoforms were expressed and purified from E. coli as MBP fusion proteins and incubated with poly I:C and [ɑ−32P] ATP for 2h before resolving by polyacrylamide gel electrophoresis (methods). Lane 1–4 are derived from reactions containing 5, 1, 0.2, or 0.04 μM OAS1, respectively. All data are representative of at least two independent experiments.
Experimentelle Infektionen Von Cercopithecus Aethiops Mit Dem Erreger Des Frankfurt.Marburg.Syndroms (Fms), supplied by Marburg GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Makoto USA Inc variations among grivet (cercopithecus aethiops aethiops) populations in central ethiopia
(A) Summary of mRNA splice variants made by individuals with the A or G variant at exon 6 splice acceptor site (rs10774671). Individuals with the A allele have lowered OAS activity (see text). (B) Tenfold serial dilutions of yeast expressing human RNase L and the indicated human OAS1 isoform imaged after 48 hours of growth on galactose medium. (C) Immunoblot analysis of OAS1, RNase L and Us11 expression from yeast (D) OAS1 Immunoblot of human cell lines A549 and a primary Human <t>Fibroblast</t> (HF) with or without IFN-α stimulation. Isoform lane is a mixture of 293T cell lysates transfected with pcDNA6 expression vector encoding human OAS1 p42 or p46 (top) Sanger sequencing traces at the OAS1 exon 6 splice junction for each cell lines are shown (bottom) (E) Gel image of ATP polymerization assay. Indicated human OAS1 isoforms were expressed and purified from E. coli as MBP fusion proteins and incubated with poly I:C and [ɑ−32P] ATP for 2h before resolving by polyacrylamide gel electrophoresis (methods). Lane 1–4 are derived from reactions containing 5, 1, 0.2, or 0.04 μM OAS1, respectively. All data are representative of at least two independent experiments.
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Zambon body mass regressions for cercopithecus aethiops
(A) Summary of mRNA splice variants made by individuals with the A or G variant at exon 6 splice acceptor site (rs10774671). Individuals with the A allele have lowered OAS activity (see text). (B) Tenfold serial dilutions of yeast expressing human RNase L and the indicated human OAS1 isoform imaged after 48 hours of growth on galactose medium. (C) Immunoblot analysis of OAS1, RNase L and Us11 expression from yeast (D) OAS1 Immunoblot of human cell lines A549 and a primary Human <t>Fibroblast</t> (HF) with or without IFN-α stimulation. Isoform lane is a mixture of 293T cell lysates transfected with pcDNA6 expression vector encoding human OAS1 p42 or p46 (top) Sanger sequencing traces at the OAS1 exon 6 splice junction for each cell lines are shown (bottom) (E) Gel image of ATP polymerization assay. Indicated human OAS1 isoforms were expressed and purified from E. coli as MBP fusion proteins and incubated with poly I:C and [ɑ−32P] ATP for 2h before resolving by polyacrylamide gel electrophoresis (methods). Lane 1–4 are derived from reactions containing 5, 1, 0.2, or 0.04 μM OAS1, respectively. All data are representative of at least two independent experiments.
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Image Search Results


(A) Summary of mRNA splice variants made by individuals with the A or G variant at exon 6 splice acceptor site (rs10774671). Individuals with the A allele have lowered OAS activity (see text). (B) Tenfold serial dilutions of yeast expressing human RNase L and the indicated human OAS1 isoform imaged after 48 hours of growth on galactose medium. (C) Immunoblot analysis of OAS1, RNase L and Us11 expression from yeast (D) OAS1 Immunoblot of human cell lines A549 and a primary Human Fibroblast (HF) with or without IFN-α stimulation. Isoform lane is a mixture of 293T cell lysates transfected with pcDNA6 expression vector encoding human OAS1 p42 or p46 (top) Sanger sequencing traces at the OAS1 exon 6 splice junction for each cell lines are shown (bottom) (E) Gel image of ATP polymerization assay. Indicated human OAS1 isoforms were expressed and purified from E. coli as MBP fusion proteins and incubated with poly I:C and [ɑ−32P] ATP for 2h before resolving by polyacrylamide gel electrophoresis (methods). Lane 1–4 are derived from reactions containing 5, 1, 0.2, or 0.04 μM OAS1, respectively. All data are representative of at least two independent experiments.

Journal: Cell host & microbe

Article Title: Recurrent loss-of-function mutations reveal costs to OAS1 antiviral activity in primates

doi: 10.1016/j.chom.2019.01.001

Figure Lengend Snippet: (A) Summary of mRNA splice variants made by individuals with the A or G variant at exon 6 splice acceptor site (rs10774671). Individuals with the A allele have lowered OAS activity (see text). (B) Tenfold serial dilutions of yeast expressing human RNase L and the indicated human OAS1 isoform imaged after 48 hours of growth on galactose medium. (C) Immunoblot analysis of OAS1, RNase L and Us11 expression from yeast (D) OAS1 Immunoblot of human cell lines A549 and a primary Human Fibroblast (HF) with or without IFN-α stimulation. Isoform lane is a mixture of 293T cell lysates transfected with pcDNA6 expression vector encoding human OAS1 p42 or p46 (top) Sanger sequencing traces at the OAS1 exon 6 splice junction for each cell lines are shown (bottom) (E) Gel image of ATP polymerization assay. Indicated human OAS1 isoforms were expressed and purified from E. coli as MBP fusion proteins and incubated with poly I:C and [ɑ−32P] ATP for 2h before resolving by polyacrylamide gel electrophoresis (methods). Lane 1–4 are derived from reactions containing 5, 1, 0.2, or 0.04 μM OAS1, respectively. All data are representative of at least two independent experiments.

Article Snippet: African Green Monkey fibroblast, male (Cercopithecus aethiops) , Coriell Institute , Cat#PR01193; RRID:CVCL 2 X98.

Techniques: Variant Assay, Activity Assay, Expressing, Western Blot, Transfection, Plasmid Preparation, Sequencing, Polymerization Assay, Purification, Incubation, Polyacrylamide Gel Electrophoresis, Derivative Assay

KEY RESOURCES TABLE

Journal: Cell host & microbe

Article Title: Recurrent loss-of-function mutations reveal costs to OAS1 antiviral activity in primates

doi: 10.1016/j.chom.2019.01.001

Figure Lengend Snippet: KEY RESOURCES TABLE

Article Snippet: African Green Monkey fibroblast, male (Cercopithecus aethiops) , Coriell Institute , Cat#PR01193; RRID:CVCL 2 X98.

Techniques: Recombinant, Expressing, Plasmid Preparation, Software