synechococcus elongatus Search Results


2007 n a s elongatus pcc 7942 wild type atcc  (ATCC)
94
ATCC 2007 n a s elongatus pcc 7942 wild type atcc
2007 N A S Elongatus Pcc 7942 Wild Type Atcc, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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type synechococcus elongatus pcc 7942 strain  (ATCC)
93
ATCC type synechococcus elongatus pcc 7942 strain
(A) In pulse-chase labeling of RbcL-SNAP in live S . elongatus cells, actively assembling carboxysomes with solvent accessible RbcL-SNAP are labeled with BG dye. Red: phase contrast. Green: RbcL. Scale bar: 1µm. (B) The distribution of the number of SNAP labeled carboxysomes, indicating active assembly, in cells directly after labeling (n=442). (C) The biogenesis of carboxysomes can be monitored from long timelapses. Red: phase contrast. Green: RbcL-GFP. Scale bar: 1µm. (D) Montage showing the formation of new carboxysome at the site of a preexisting carboxysome. White arrow indicates the birth event. Panel height: 25 pixels. Time interval: 3 minutes. (E–F) RuBisCO foci elongate into bar carboxysomes that subsequently split into two carboxysomes. Scale bar: 1µm. Time interval: 75 minutes. (G–I) Kymographs of RbcL-GFP in growing and dividing cells. Carboxysome birth events are indicated by white arrows. Scale bar: 1µm. Time interval: 3 minutes. (J) Spatial distribution of 234 birth events along the long axis of the cell. Quarter cell positions are favored. (K) Relative intensity of 141 pairs of new (daughter) carboxysomes and the preexisting carboxysomes to which they initially colocalize (mothers) reveals that birth events are highly asymmetric, with mean daughter intensity being 1/4 that of the mother. Because pairs are sorted into dim (daughter) and bright (mother) pairs, no data points can fall into the shaded area. Dotted line indicates a 1:4 ratio.
Type Synechococcus Elongatus Pcc 7942 Strain, supplied by ATCC, 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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s elongatus strain pcc 7942 genomic dna  (ATCC)
93
ATCC s elongatus strain pcc 7942 genomic dna
(A) In pulse-chase labeling of RbcL-SNAP in live S . elongatus cells, actively assembling carboxysomes with solvent accessible RbcL-SNAP are labeled with BG dye. Red: phase contrast. Green: RbcL. Scale bar: 1µm. (B) The distribution of the number of SNAP labeled carboxysomes, indicating active assembly, in cells directly after labeling (n=442). (C) The biogenesis of carboxysomes can be monitored from long timelapses. Red: phase contrast. Green: RbcL-GFP. Scale bar: 1µm. (D) Montage showing the formation of new carboxysome at the site of a preexisting carboxysome. White arrow indicates the birth event. Panel height: 25 pixels. Time interval: 3 minutes. (E–F) RuBisCO foci elongate into bar carboxysomes that subsequently split into two carboxysomes. Scale bar: 1µm. Time interval: 75 minutes. (G–I) Kymographs of RbcL-GFP in growing and dividing cells. Carboxysome birth events are indicated by white arrows. Scale bar: 1µm. Time interval: 3 minutes. (J) Spatial distribution of 234 birth events along the long axis of the cell. Quarter cell positions are favored. (K) Relative intensity of 141 pairs of new (daughter) carboxysomes and the preexisting carboxysomes to which they initially colocalize (mothers) reveals that birth events are highly asymmetric, with mean daughter intensity being 1/4 that of the mother. Because pairs are sorted into dim (daughter) and bright (mother) pairs, no data points can fall into the shaded area. Dotted line indicates a 1:4 ratio.
S Elongatus Strain Pcc 7942 Genomic Dna, supplied by ATCC, 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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coding sequence of synechococcus elongatus pcc 6301 cpct  (GenScript corporation)
90
GenScript corporation coding sequence of synechococcus elongatus pcc 6301 cpct
(A) In pulse-chase labeling of RbcL-SNAP in live S . elongatus cells, actively assembling carboxysomes with solvent accessible RbcL-SNAP are labeled with BG dye. Red: phase contrast. Green: RbcL. Scale bar: 1µm. (B) The distribution of the number of SNAP labeled carboxysomes, indicating active assembly, in cells directly after labeling (n=442). (C) The biogenesis of carboxysomes can be monitored from long timelapses. Red: phase contrast. Green: RbcL-GFP. Scale bar: 1µm. (D) Montage showing the formation of new carboxysome at the site of a preexisting carboxysome. White arrow indicates the birth event. Panel height: 25 pixels. Time interval: 3 minutes. (E–F) RuBisCO foci elongate into bar carboxysomes that subsequently split into two carboxysomes. Scale bar: 1µm. Time interval: 75 minutes. (G–I) Kymographs of RbcL-GFP in growing and dividing cells. Carboxysome birth events are indicated by white arrows. Scale bar: 1µm. Time interval: 3 minutes. (J) Spatial distribution of 234 birth events along the long axis of the cell. Quarter cell positions are favored. (K) Relative intensity of 141 pairs of new (daughter) carboxysomes and the preexisting carboxysomes to which they initially colocalize (mothers) reveals that birth events are highly asymmetric, with mean daughter intensity being 1/4 that of the mother. Because pairs are sorted into dim (daughter) and bright (mother) pairs, no data points can fall into the shaded area. Dotted line indicates a 1:4 ratio.
Coding Sequence Of Synechococcus Elongatus Pcc 6301 Cpct, supplied by GenScript corporation, 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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synechococcus elongatus pcc 7942 psba3 gene sequence  (Biotechnology Information)
90
Biotechnology Information synechococcus elongatus pcc 7942 psba3 gene sequence
(A) In pulse-chase labeling of RbcL-SNAP in live S . elongatus cells, actively assembling carboxysomes with solvent accessible RbcL-SNAP are labeled with BG dye. Red: phase contrast. Green: RbcL. Scale bar: 1µm. (B) The distribution of the number of SNAP labeled carboxysomes, indicating active assembly, in cells directly after labeling (n=442). (C) The biogenesis of carboxysomes can be monitored from long timelapses. Red: phase contrast. Green: RbcL-GFP. Scale bar: 1µm. (D) Montage showing the formation of new carboxysome at the site of a preexisting carboxysome. White arrow indicates the birth event. Panel height: 25 pixels. Time interval: 3 minutes. (E–F) RuBisCO foci elongate into bar carboxysomes that subsequently split into two carboxysomes. Scale bar: 1µm. Time interval: 75 minutes. (G–I) Kymographs of RbcL-GFP in growing and dividing cells. Carboxysome birth events are indicated by white arrows. Scale bar: 1µm. Time interval: 3 minutes. (J) Spatial distribution of 234 birth events along the long axis of the cell. Quarter cell positions are favored. (K) Relative intensity of 141 pairs of new (daughter) carboxysomes and the preexisting carboxysomes to which they initially colocalize (mothers) reveals that birth events are highly asymmetric, with mean daughter intensity being 1/4 that of the mother. Because pairs are sorted into dim (daughter) and bright (mother) pairs, no data points can fall into the shaded area. Dotted line indicates a 1:4 ratio.
Synechococcus Elongatus Pcc 7942 Psba3 Gene Sequence, supplied by Biotechnology Information, 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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synechococcus elongatus pcc 7942  (BioMimetic Therapeutics)
90
BioMimetic Therapeutics synechococcus elongatus pcc 7942
(A) In pulse-chase labeling of RbcL-SNAP in live S . elongatus cells, actively assembling carboxysomes with solvent accessible RbcL-SNAP are labeled with BG dye. Red: phase contrast. Green: RbcL. Scale bar: 1µm. (B) The distribution of the number of SNAP labeled carboxysomes, indicating active assembly, in cells directly after labeling (n=442). (C) The biogenesis of carboxysomes can be monitored from long timelapses. Red: phase contrast. Green: RbcL-GFP. Scale bar: 1µm. (D) Montage showing the formation of new carboxysome at the site of a preexisting carboxysome. White arrow indicates the birth event. Panel height: 25 pixels. Time interval: 3 minutes. (E–F) RuBisCO foci elongate into bar carboxysomes that subsequently split into two carboxysomes. Scale bar: 1µm. Time interval: 75 minutes. (G–I) Kymographs of RbcL-GFP in growing and dividing cells. Carboxysome birth events are indicated by white arrows. Scale bar: 1µm. Time interval: 3 minutes. (J) Spatial distribution of 234 birth events along the long axis of the cell. Quarter cell positions are favored. (K) Relative intensity of 141 pairs of new (daughter) carboxysomes and the preexisting carboxysomes to which they initially colocalize (mothers) reveals that birth events are highly asymmetric, with mean daughter intensity being 1/4 that of the mother. Because pairs are sorted into dim (daughter) and bright (mother) pairs, no data points can fall into the shaded area. Dotted line indicates a 1:4 ratio.
Synechococcus Elongatus Pcc 7942, supplied by BioMimetic Therapeutics, 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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antibodies raised against clpc from synechococcus elongatus  (Agrisera)
90
Agrisera antibodies raised against clpc from synechococcus elongatus
(A) In pulse-chase labeling of RbcL-SNAP in live S . elongatus cells, actively assembling carboxysomes with solvent accessible RbcL-SNAP are labeled with BG dye. Red: phase contrast. Green: RbcL. Scale bar: 1µm. (B) The distribution of the number of SNAP labeled carboxysomes, indicating active assembly, in cells directly after labeling (n=442). (C) The biogenesis of carboxysomes can be monitored from long timelapses. Red: phase contrast. Green: RbcL-GFP. Scale bar: 1µm. (D) Montage showing the formation of new carboxysome at the site of a preexisting carboxysome. White arrow indicates the birth event. Panel height: 25 pixels. Time interval: 3 minutes. (E–F) RuBisCO foci elongate into bar carboxysomes that subsequently split into two carboxysomes. Scale bar: 1µm. Time interval: 75 minutes. (G–I) Kymographs of RbcL-GFP in growing and dividing cells. Carboxysome birth events are indicated by white arrows. Scale bar: 1µm. Time interval: 3 minutes. (J) Spatial distribution of 234 birth events along the long axis of the cell. Quarter cell positions are favored. (K) Relative intensity of 141 pairs of new (daughter) carboxysomes and the preexisting carboxysomes to which they initially colocalize (mothers) reveals that birth events are highly asymmetric, with mean daughter intensity being 1/4 that of the mother. Because pairs are sorted into dim (daughter) and bright (mother) pairs, no data points can fall into the shaded area. Dotted line indicates a 1:4 ratio.
Antibodies Raised Against Clpc From Synechococcus Elongatus, supplied by Agrisera, 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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nira promoter (seq id no: 32) from synechococcus elongatus pcc 7942  (Blue Heron Biotech)
90
Blue Heron Biotech nira promoter (seq id no: 32) from synechococcus elongatus pcc 7942
(A) In pulse-chase labeling of RbcL-SNAP in live S . elongatus cells, actively assembling carboxysomes with solvent accessible RbcL-SNAP are labeled with BG dye. Red: phase contrast. Green: RbcL. Scale bar: 1µm. (B) The distribution of the number of SNAP labeled carboxysomes, indicating active assembly, in cells directly after labeling (n=442). (C) The biogenesis of carboxysomes can be monitored from long timelapses. Red: phase contrast. Green: RbcL-GFP. Scale bar: 1µm. (D) Montage showing the formation of new carboxysome at the site of a preexisting carboxysome. White arrow indicates the birth event. Panel height: 25 pixels. Time interval: 3 minutes. (E–F) RuBisCO foci elongate into bar carboxysomes that subsequently split into two carboxysomes. Scale bar: 1µm. Time interval: 75 minutes. (G–I) Kymographs of RbcL-GFP in growing and dividing cells. Carboxysome birth events are indicated by white arrows. Scale bar: 1µm. Time interval: 3 minutes. (J) Spatial distribution of 234 birth events along the long axis of the cell. Quarter cell positions are favored. (K) Relative intensity of 141 pairs of new (daughter) carboxysomes and the preexisting carboxysomes to which they initially colocalize (mothers) reveals that birth events are highly asymmetric, with mean daughter intensity being 1/4 that of the mother. Because pairs are sorted into dim (daughter) and bright (mother) pairs, no data points can fall into the shaded area. Dotted line indicates a 1:4 ratio.
Nira Promoter (Seq Id No: 32) From Synechococcus Elongatus Pcc 7942, supplied by Blue Heron Biotech, 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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dna sequences coding for ccmk3 and ccmk4 from synechococcus elongatus pcc7942  (Twist Bioscience)
90
Twist Bioscience dna sequences coding for ccmk3 and ccmk4 from synechococcus elongatus pcc7942
(A) In pulse-chase labeling of RbcL-SNAP in live S . elongatus cells, actively assembling carboxysomes with solvent accessible RbcL-SNAP are labeled with BG dye. Red: phase contrast. Green: RbcL. Scale bar: 1µm. (B) The distribution of the number of SNAP labeled carboxysomes, indicating active assembly, in cells directly after labeling (n=442). (C) The biogenesis of carboxysomes can be monitored from long timelapses. Red: phase contrast. Green: RbcL-GFP. Scale bar: 1µm. (D) Montage showing the formation of new carboxysome at the site of a preexisting carboxysome. White arrow indicates the birth event. Panel height: 25 pixels. Time interval: 3 minutes. (E–F) RuBisCO foci elongate into bar carboxysomes that subsequently split into two carboxysomes. Scale bar: 1µm. Time interval: 75 minutes. (G–I) Kymographs of RbcL-GFP in growing and dividing cells. Carboxysome birth events are indicated by white arrows. Scale bar: 1µm. Time interval: 3 minutes. (J) Spatial distribution of 234 birth events along the long axis of the cell. Quarter cell positions are favored. (K) Relative intensity of 141 pairs of new (daughter) carboxysomes and the preexisting carboxysomes to which they initially colocalize (mothers) reveals that birth events are highly asymmetric, with mean daughter intensity being 1/4 that of the mother. Because pairs are sorted into dim (daughter) and bright (mother) pairs, no data points can fall into the shaded area. Dotted line indicates a 1:4 ratio.
Dna Sequences Coding For Ccmk3 And Ccmk4 From Synechococcus Elongatus Pcc7942, supplied by Twist Bioscience, 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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synechococcus elongatus strain sag 89.79  (Algen Biopharmaceuticals Inc)
90
Algen Biopharmaceuticals Inc synechococcus elongatus strain sag 89.79
(A) In pulse-chase labeling of RbcL-SNAP in live S . elongatus cells, actively assembling carboxysomes with solvent accessible RbcL-SNAP are labeled with BG dye. Red: phase contrast. Green: RbcL. Scale bar: 1µm. (B) The distribution of the number of SNAP labeled carboxysomes, indicating active assembly, in cells directly after labeling (n=442). (C) The biogenesis of carboxysomes can be monitored from long timelapses. Red: phase contrast. Green: RbcL-GFP. Scale bar: 1µm. (D) Montage showing the formation of new carboxysome at the site of a preexisting carboxysome. White arrow indicates the birth event. Panel height: 25 pixels. Time interval: 3 minutes. (E–F) RuBisCO foci elongate into bar carboxysomes that subsequently split into two carboxysomes. Scale bar: 1µm. Time interval: 75 minutes. (G–I) Kymographs of RbcL-GFP in growing and dividing cells. Carboxysome birth events are indicated by white arrows. Scale bar: 1µm. Time interval: 3 minutes. (J) Spatial distribution of 234 birth events along the long axis of the cell. Quarter cell positions are favored. (K) Relative intensity of 141 pairs of new (daughter) carboxysomes and the preexisting carboxysomes to which they initially colocalize (mothers) reveals that birth events are highly asymmetric, with mean daughter intensity being 1/4 that of the mother. Because pairs are sorted into dim (daughter) and bright (mother) pairs, no data points can fall into the shaded area. Dotted line indicates a 1:4 ratio.
Synechococcus Elongatus Strain Sag 89.79, supplied by Algen Biopharmaceuticals Inc, 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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sucrose-secreting synechococcus elongatus fl130  (BioProcess Technology Consultants)
90
BioProcess Technology Consultants sucrose-secreting synechococcus elongatus fl130
(A) In pulse-chase labeling of RbcL-SNAP in live S . elongatus cells, actively assembling carboxysomes with solvent accessible RbcL-SNAP are labeled with BG dye. Red: phase contrast. Green: RbcL. Scale bar: 1µm. (B) The distribution of the number of SNAP labeled carboxysomes, indicating active assembly, in cells directly after labeling (n=442). (C) The biogenesis of carboxysomes can be monitored from long timelapses. Red: phase contrast. Green: RbcL-GFP. Scale bar: 1µm. (D) Montage showing the formation of new carboxysome at the site of a preexisting carboxysome. White arrow indicates the birth event. Panel height: 25 pixels. Time interval: 3 minutes. (E–F) RuBisCO foci elongate into bar carboxysomes that subsequently split into two carboxysomes. Scale bar: 1µm. Time interval: 75 minutes. (G–I) Kymographs of RbcL-GFP in growing and dividing cells. Carboxysome birth events are indicated by white arrows. Scale bar: 1µm. Time interval: 3 minutes. (J) Spatial distribution of 234 birth events along the long axis of the cell. Quarter cell positions are favored. (K) Relative intensity of 141 pairs of new (daughter) carboxysomes and the preexisting carboxysomes to which they initially colocalize (mothers) reveals that birth events are highly asymmetric, with mean daughter intensity being 1/4 that of the mother. Because pairs are sorted into dim (daughter) and bright (mother) pairs, no data points can fall into the shaded area. Dotted line indicates a 1:4 ratio.
Sucrose Secreting Synechococcus Elongatus Fl130, supplied by BioProcess Technology Consultants, 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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synechococcus elongatus pcc 7942  (Baier labs)
90
Baier labs synechococcus elongatus pcc 7942
(A) In pulse-chase labeling of RbcL-SNAP in live S . elongatus cells, actively assembling carboxysomes with solvent accessible RbcL-SNAP are labeled with BG dye. Red: phase contrast. Green: RbcL. Scale bar: 1µm. (B) The distribution of the number of SNAP labeled carboxysomes, indicating active assembly, in cells directly after labeling (n=442). (C) The biogenesis of carboxysomes can be monitored from long timelapses. Red: phase contrast. Green: RbcL-GFP. Scale bar: 1µm. (D) Montage showing the formation of new carboxysome at the site of a preexisting carboxysome. White arrow indicates the birth event. Panel height: 25 pixels. Time interval: 3 minutes. (E–F) RuBisCO foci elongate into bar carboxysomes that subsequently split into two carboxysomes. Scale bar: 1µm. Time interval: 75 minutes. (G–I) Kymographs of RbcL-GFP in growing and dividing cells. Carboxysome birth events are indicated by white arrows. Scale bar: 1µm. Time interval: 3 minutes. (J) Spatial distribution of 234 birth events along the long axis of the cell. Quarter cell positions are favored. (K) Relative intensity of 141 pairs of new (daughter) carboxysomes and the preexisting carboxysomes to which they initially colocalize (mothers) reveals that birth events are highly asymmetric, with mean daughter intensity being 1/4 that of the mother. Because pairs are sorted into dim (daughter) and bright (mother) pairs, no data points can fall into the shaded area. Dotted line indicates a 1:4 ratio.
Synechococcus Elongatus Pcc 7942, supplied by Baier labs, 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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synechococcus elongatus pcc 7942 - by Bioz Stars, 2026-03
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Image Search Results


(A) In pulse-chase labeling of RbcL-SNAP in live S . elongatus cells, actively assembling carboxysomes with solvent accessible RbcL-SNAP are labeled with BG dye. Red: phase contrast. Green: RbcL. Scale bar: 1µm. (B) The distribution of the number of SNAP labeled carboxysomes, indicating active assembly, in cells directly after labeling (n=442). (C) The biogenesis of carboxysomes can be monitored from long timelapses. Red: phase contrast. Green: RbcL-GFP. Scale bar: 1µm. (D) Montage showing the formation of new carboxysome at the site of a preexisting carboxysome. White arrow indicates the birth event. Panel height: 25 pixels. Time interval: 3 minutes. (E–F) RuBisCO foci elongate into bar carboxysomes that subsequently split into two carboxysomes. Scale bar: 1µm. Time interval: 75 minutes. (G–I) Kymographs of RbcL-GFP in growing and dividing cells. Carboxysome birth events are indicated by white arrows. Scale bar: 1µm. Time interval: 3 minutes. (J) Spatial distribution of 234 birth events along the long axis of the cell. Quarter cell positions are favored. (K) Relative intensity of 141 pairs of new (daughter) carboxysomes and the preexisting carboxysomes to which they initially colocalize (mothers) reveals that birth events are highly asymmetric, with mean daughter intensity being 1/4 that of the mother. Because pairs are sorted into dim (daughter) and bright (mother) pairs, no data points can fall into the shaded area. Dotted line indicates a 1:4 ratio.

Journal: PLoS ONE

Article Title: The Bacterial Carbon-Fixing Organelle Is Formed by Shell Envelopment of Preassembled Cargo

doi: 10.1371/journal.pone.0076127

Figure Lengend Snippet: (A) In pulse-chase labeling of RbcL-SNAP in live S . elongatus cells, actively assembling carboxysomes with solvent accessible RbcL-SNAP are labeled with BG dye. Red: phase contrast. Green: RbcL. Scale bar: 1µm. (B) The distribution of the number of SNAP labeled carboxysomes, indicating active assembly, in cells directly after labeling (n=442). (C) The biogenesis of carboxysomes can be monitored from long timelapses. Red: phase contrast. Green: RbcL-GFP. Scale bar: 1µm. (D) Montage showing the formation of new carboxysome at the site of a preexisting carboxysome. White arrow indicates the birth event. Panel height: 25 pixels. Time interval: 3 minutes. (E–F) RuBisCO foci elongate into bar carboxysomes that subsequently split into two carboxysomes. Scale bar: 1µm. Time interval: 75 minutes. (G–I) Kymographs of RbcL-GFP in growing and dividing cells. Carboxysome birth events are indicated by white arrows. Scale bar: 1µm. Time interval: 3 minutes. (J) Spatial distribution of 234 birth events along the long axis of the cell. Quarter cell positions are favored. (K) Relative intensity of 141 pairs of new (daughter) carboxysomes and the preexisting carboxysomes to which they initially colocalize (mothers) reveals that birth events are highly asymmetric, with mean daughter intensity being 1/4 that of the mother. Because pairs are sorted into dim (daughter) and bright (mother) pairs, no data points can fall into the shaded area. Dotted line indicates a 1:4 ratio.

Article Snippet: The wild-type Synechococcus elongatus PCC 7942 strain was acquired from the American Type Culture Collection (ATCC, Manassas, VA).

Techniques: Pulse Chase, Labeling, Solvent

Bacterial Strains and Plasmids.

Journal: PLoS ONE

Article Title: The Bacterial Carbon-Fixing Organelle Is Formed by Shell Envelopment of Preassembled Cargo

doi: 10.1371/journal.pone.0076127

Figure Lengend Snippet: Bacterial Strains and Plasmids.

Article Snippet: The wild-type Synechococcus elongatus PCC 7942 strain was acquired from the American Type Culture Collection (ATCC, Manassas, VA).

Techniques: Plasmid Preparation, Clone Assay