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Bethyl rabbit polyclonal anti rps3

Rabbit Polyclonal Anti Rps3, supplied by Bethyl, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
rabbit polyclonal anti rps3 - by Bioz Stars, 2025-02
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1) Product Images from "Unresolved stalled ribosome complexes restrict cell-cycle progression after genotoxic stress"

Article Title: Unresolved stalled ribosome complexes restrict cell-cycle progression after genotoxic stress

Journal: Molecular Cell

doi: 10.1016/j.molcel.2022.01.019


Figure Legend Snippet:

Techniques Used: Recombinant, Protease Inhibitor, Binding Assay, Staining, Western Blot, Mutagenesis, Mass Spectrometry, Software, Magnetic Beads



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Glyphosate exposure damages Golgi apparatus distribution and ribosome functions in porcine oocytes. A Representative images of Golgi apparatus distribution in control and 400 μmol/L glyphosate treatment groups. Bar = 30 μm. B The relative florescence intensity of Golgi apparatus after 400 μmol/L glyphosate treatment. *, P < 0.05. C Western blot analysis for the protein expression of GM130 in control and 400 μmol/L glyphosate exposure groups. ns: no significance. D Representative images of ribosome distribution in control and 400 μmol/L glyphosate treatment groups. Bar = 30 μm. E The relative florescence intensity of <t>RPS3</t> after 400 μmol/L glyphosate treatment. **, P < 0.01
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ACR decreases the distribution of ribosome protein <t>Rps3</t> and ER in oocytes. (A) The typical fluorescence picture of ribosome protein Rps3 after ACR treatment. Rps3 diffused from the spindle periphery after ACR exposure compared with the control group. Green, Rps3; blue, DNA. Bar = 30 μm. (B) The fluorescence intensity of Rps3 after ACR exposure was significantly higher than that of the control group. * p < 0.05. (C) The typical picture for the distribution of ER after ACR treatment. Similar to ribosome, the ER diffused from the spindle periphery after ACR exposure compared with the control group. Red, ER-Tracker. Bar = 30 μm. (D) The abnormal rate of ER increased significantly in the 5 mM ACR group compared with the control group. *** p < 0.001.
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MYCT1 interacts with RACK1 and affected the enrichment of RACK1 on ribosomes (A) GO/KEGG analyses of MYCT1-targeted immunoprecipitation followed by mass spectrometry in mouse liver tissues. (B) Co-immunoprecipitation of MYCT1 and RACK1 in WT/ Myct1 KO mice liver tissues. (C) Co-immunoprecipitation of MYCT1 and RACK1 in lentivirus-over MYCT1/control HepG2 cells. (D) Representative polysome profile (top) complemented with RACK1 from WT/ Myct1 KO mice liver tissues. The fractions were analyzed by immunoblotting. (E) Representative polysome profile (top) complemented with RACK1 from lentivirus-MYCT1/control HepG2 cells. The fractions were analyzed by immunoblotting. (F) Immunofluorescence stain of RACK1 and <t>RPS3</t> in lentivirus-overMYCT1/control HepG2 cells. Scale bar: 50 μm.
Rabbit Polyclonal Anti Rps3, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
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Image Search Results


Glyphosate exposure damages Golgi apparatus distribution and ribosome functions in porcine oocytes. A Representative images of Golgi apparatus distribution in control and 400 μmol/L glyphosate treatment groups. Bar = 30 μm. B The relative florescence intensity of Golgi apparatus after 400 μmol/L glyphosate treatment. *, P < 0.05. C Western blot analysis for the protein expression of GM130 in control and 400 μmol/L glyphosate exposure groups. ns: no significance. D Representative images of ribosome distribution in control and 400 μmol/L glyphosate treatment groups. Bar = 30 μm. E The relative florescence intensity of RPS3 after 400 μmol/L glyphosate treatment. **, P < 0.01

Journal: Journal of Animal Science and Biotechnology

Article Title: Glyphosate exposure deteriorates oocyte meiotic maturation via induction of organelle dysfunctions in pigs

doi: 10.1186/s40104-022-00732-0

Figure Lengend Snippet: Glyphosate exposure damages Golgi apparatus distribution and ribosome functions in porcine oocytes. A Representative images of Golgi apparatus distribution in control and 400 μmol/L glyphosate treatment groups. Bar = 30 μm. B The relative florescence intensity of Golgi apparatus after 400 μmol/L glyphosate treatment. *, P < 0.05. C Western blot analysis for the protein expression of GM130 in control and 400 μmol/L glyphosate exposure groups. ns: no significance. D Representative images of ribosome distribution in control and 400 μmol/L glyphosate treatment groups. Bar = 30 μm. E The relative florescence intensity of RPS3 after 400 μmol/L glyphosate treatment. **, P < 0.01

Article Snippet: Rabbit polyclonal anti-LAMP2 antibody (27823–1-AP), rabbit polyclonal anti-GRP78 antibody (11587-AP-1) and rabbit polyclonal anti-RPS3 antibody (11990–1-AP) were purchased from Proteintech (Chicago, IL, USA).

Techniques: Western Blot, Expressing

Journal: Molecular Cell

Article Title: Unresolved stalled ribosome complexes restrict cell-cycle progression after genotoxic stress

doi: 10.1016/j.molcel.2022.01.019

Figure Lengend Snippet:

Article Snippet: Rabbit polyclonal anti-rpS3 , Bethyl , Cat. #A303-840A; RRID: AB_2620191.

Techniques: Recombinant, Protease Inhibitor, Binding Assay, Staining, Western Blot, Mutagenesis, Mass Spectrometry, Software, Magnetic Beads

ACR decreases the distribution of ribosome protein Rps3 and ER in oocytes. (A) The typical fluorescence picture of ribosome protein Rps3 after ACR treatment. Rps3 diffused from the spindle periphery after ACR exposure compared with the control group. Green, Rps3; blue, DNA. Bar = 30 μm. (B) The fluorescence intensity of Rps3 after ACR exposure was significantly higher than that of the control group. * p < 0.05. (C) The typical picture for the distribution of ER after ACR treatment. Similar to ribosome, the ER diffused from the spindle periphery after ACR exposure compared with the control group. Red, ER-Tracker. Bar = 30 μm. (D) The abnormal rate of ER increased significantly in the 5 mM ACR group compared with the control group. *** p < 0.001.

Journal: Frontiers in Cell and Developmental Biology

Article Title: Acrylamide Exposure Destroys the Distribution and Functions of Organelles in Mouse Oocytes

doi: 10.3389/fcell.2022.834964

Figure Lengend Snippet: ACR decreases the distribution of ribosome protein Rps3 and ER in oocytes. (A) The typical fluorescence picture of ribosome protein Rps3 after ACR treatment. Rps3 diffused from the spindle periphery after ACR exposure compared with the control group. Green, Rps3; blue, DNA. Bar = 30 μm. (B) The fluorescence intensity of Rps3 after ACR exposure was significantly higher than that of the control group. * p < 0.05. (C) The typical picture for the distribution of ER after ACR treatment. Similar to ribosome, the ER diffused from the spindle periphery after ACR exposure compared with the control group. Red, ER-Tracker. Bar = 30 μm. (D) The abnormal rate of ER increased significantly in the 5 mM ACR group compared with the control group. *** p < 0.001.

Article Snippet: Three antibodies were used for the current experiments: rabbit polyclonal anti-LAMP2 antibody (1:100) (no: 27823-1-AP, Proteintech, United States), rabbit polyclonal anti-Rab8A antibody (1:100) (ab188574, Abcam, UK), and rabbit polyclonal anti-Rps3 antibody (1:500) (ab181992, Abcam, UK), fluorescent anti-rabbit antibodies were purchased from Invitrogen (Carlsbad, CA, United States), and Hoechst 33342 and other reagents were purchased from Sigma Aldrich Corp.

Techniques: Fluorescence

MYCT1 interacts with RACK1 and affected the enrichment of RACK1 on ribosomes (A) GO/KEGG analyses of MYCT1-targeted immunoprecipitation followed by mass spectrometry in mouse liver tissues. (B) Co-immunoprecipitation of MYCT1 and RACK1 in WT/ Myct1 KO mice liver tissues. (C) Co-immunoprecipitation of MYCT1 and RACK1 in lentivirus-over MYCT1/control HepG2 cells. (D) Representative polysome profile (top) complemented with RACK1 from WT/ Myct1 KO mice liver tissues. The fractions were analyzed by immunoblotting. (E) Representative polysome profile (top) complemented with RACK1 from lentivirus-MYCT1/control HepG2 cells. The fractions were analyzed by immunoblotting. (F) Immunofluorescence stain of RACK1 and RPS3 in lentivirus-overMYCT1/control HepG2 cells. Scale bar: 50 μm.

Journal: iScience

Article Title: MYCT1 alters the glycogen shunt by regulating selective translation of RACK1-mediated enzymes

doi: 10.1016/j.isci.2022.103955

Figure Lengend Snippet: MYCT1 interacts with RACK1 and affected the enrichment of RACK1 on ribosomes (A) GO/KEGG analyses of MYCT1-targeted immunoprecipitation followed by mass spectrometry in mouse liver tissues. (B) Co-immunoprecipitation of MYCT1 and RACK1 in WT/ Myct1 KO mice liver tissues. (C) Co-immunoprecipitation of MYCT1 and RACK1 in lentivirus-over MYCT1/control HepG2 cells. (D) Representative polysome profile (top) complemented with RACK1 from WT/ Myct1 KO mice liver tissues. The fractions were analyzed by immunoblotting. (E) Representative polysome profile (top) complemented with RACK1 from lentivirus-MYCT1/control HepG2 cells. The fractions were analyzed by immunoblotting. (F) Immunofluorescence stain of RACK1 and RPS3 in lentivirus-overMYCT1/control HepG2 cells. Scale bar: 50 μm.

Article Snippet: Rabbit polyclonal anti-RPS3 , ProteinTech , Cat# 11990-1-AP; RRID: AB_2180758.

Techniques: Immunoprecipitation, Mass Spectrometry, Western Blot, Immunofluorescence, Staining

Journal: iScience

Article Title: MYCT1 alters the glycogen shunt by regulating selective translation of RACK1-mediated enzymes

doi: 10.1016/j.isci.2022.103955

Figure Lengend Snippet:

Article Snippet: Rabbit polyclonal anti-RPS3 , ProteinTech , Cat# 11990-1-AP; RRID: AB_2180758.

Techniques: Clone Assay, Recombinant, Protease Inhibitor, Staining, Bicinchoninic Acid Protein Assay, Colorimetric Assay, Enzyme-linked Immunosorbent Assay, Immunoprecipitation, Mass Spectrometry, Negative Control, Software