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penicillium nalgiovense  (ATCC)
93
ATCC penicillium nalgiovense
Strains used in fermentation.
Penicillium Nalgiovense, 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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aphidicolin  (Thermo Fisher)
94
Thermo Fisher aphidicolin
E10.5 embryonic tails were cultured ex vivo and treated with DMSO or the cell cycle inhibitor <t>Aphidicolin.</t> A-C After 23 hr of incubation, tails were fixed and stained for Brachyury and counterstained with DAPI. Scale bar 100 µm. A Representative images. B Quantification of the Brachyury signal along the AP axis of the PSM. Signal was normalized between 0 and 1. n(DMSO) = 6, n(Aphidicolin) = 11. C Quantification of the length of Brachyury gradient (Line: mean, shading: standard deviation). Intensity normalized between 0 and 1. * < 0.05; *** < 0.001; **** <0.0001. D,E Fluorescence real-time imaging of embryonic tails expressing Achilles-Hes7 was performed. D Representative kymographs of control and Aphidicolin-treated samples. E Quantification of PSM length by determining the size of the oscillating field (Line: mean, shading: standard deviation). Length normalized to the PSM length at experiment start. n(DMSO) = 9, n(Aphidicolin) = 11? F After 23 hr of incubation, tails were fixed and HCR against Hes7 and Uncx4.1 as well as counterstaining with DAPI were performed. Representative images are shown (same as in Fig. S14J). G-J After 23 hr of incubation, tails were fixed and stained with DAPI. G Representative images are shown. H-J Quantification of PSM length from tail tip to last formed somite boundary ( H ), somite length ( I ) and the ratio of somite length to PSM length as a measure of scaling ( J ). K Quantification of cell motility in fluorescence real-time imaging data of embryonic tails expressing Achilles-Hes7 (data corresponds to D,E). L Schematic model of how coupling of cell proliferation to segmentation clock affects somitogenesis.
Aphidicolin, supplied by Thermo Fisher, 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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atcc 46455  (ATCC)
93
ATCC atcc 46455
E10.5 embryonic tails were cultured ex vivo and treated with DMSO or the cell cycle inhibitor <t>Aphidicolin.</t> A-C After 23 hr of incubation, tails were fixed and stained for Brachyury and counterstained with DAPI. Scale bar 100 µm. A Representative images. B Quantification of the Brachyury signal along the AP axis of the PSM. Signal was normalized between 0 and 1. n(DMSO) = 6, n(Aphidicolin) = 11. C Quantification of the length of Brachyury gradient (Line: mean, shading: standard deviation). Intensity normalized between 0 and 1. * < 0.05; *** < 0.001; **** <0.0001. D,E Fluorescence real-time imaging of embryonic tails expressing Achilles-Hes7 was performed. D Representative kymographs of control and Aphidicolin-treated samples. E Quantification of PSM length by determining the size of the oscillating field (Line: mean, shading: standard deviation). Length normalized to the PSM length at experiment start. n(DMSO) = 9, n(Aphidicolin) = 11? F After 23 hr of incubation, tails were fixed and HCR against Hes7 and Uncx4.1 as well as counterstaining with DAPI were performed. Representative images are shown (same as in Fig. S14J). G-J After 23 hr of incubation, tails were fixed and stained with DAPI. G Representative images are shown. H-J Quantification of PSM length from tail tip to last formed somite boundary ( H ), somite length ( I ) and the ratio of somite length to PSM length as a measure of scaling ( J ). K Quantification of cell motility in fluorescence real-time imaging data of embryonic tails expressing Achilles-Hes7 (data corresponds to D,E). L Schematic model of how coupling of cell proliferation to segmentation clock affects somitogenesis.
Atcc 46455, 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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af293 af293 atcc46455  (ATCC)
93
ATCC af293 af293 atcc46455
E10.5 embryonic tails were cultured ex vivo and treated with DMSO or the cell cycle inhibitor <t>Aphidicolin.</t> A-C After 23 hr of incubation, tails were fixed and stained for Brachyury and counterstained with DAPI. Scale bar 100 µm. A Representative images. B Quantification of the Brachyury signal along the AP axis of the PSM. Signal was normalized between 0 and 1. n(DMSO) = 6, n(Aphidicolin) = 11. C Quantification of the length of Brachyury gradient (Line: mean, shading: standard deviation). Intensity normalized between 0 and 1. * < 0.05; *** < 0.001; **** <0.0001. D,E Fluorescence real-time imaging of embryonic tails expressing Achilles-Hes7 was performed. D Representative kymographs of control and Aphidicolin-treated samples. E Quantification of PSM length by determining the size of the oscillating field (Line: mean, shading: standard deviation). Length normalized to the PSM length at experiment start. n(DMSO) = 9, n(Aphidicolin) = 11? F After 23 hr of incubation, tails were fixed and HCR against Hes7 and Uncx4.1 as well as counterstaining with DAPI were performed. Representative images are shown (same as in Fig. S14J). G-J After 23 hr of incubation, tails were fixed and stained with DAPI. G Representative images are shown. H-J Quantification of PSM length from tail tip to last formed somite boundary ( H ), somite length ( I ) and the ratio of somite length to PSM length as a measure of scaling ( J ). K Quantification of cell motility in fluorescence real-time imaging data of embryonic tails expressing Achilles-Hes7 (data corresponds to D,E). L Schematic model of how coupling of cell proliferation to segmentation clock affects somitogenesis.
Af293 Af293 Atcc46455, 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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lb thermofisher waltham massachusetts  (Thermo Fisher)
94
Thermo Fisher lb thermofisher waltham massachusetts
E10.5 embryonic tails were cultured ex vivo and treated with DMSO or the cell cycle inhibitor <t>Aphidicolin.</t> A-C After 23 hr of incubation, tails were fixed and stained for Brachyury and counterstained with DAPI. Scale bar 100 µm. A Representative images. B Quantification of the Brachyury signal along the AP axis of the PSM. Signal was normalized between 0 and 1. n(DMSO) = 6, n(Aphidicolin) = 11. C Quantification of the length of Brachyury gradient (Line: mean, shading: standard deviation). Intensity normalized between 0 and 1. * < 0.05; *** < 0.001; **** <0.0001. D,E Fluorescence real-time imaging of embryonic tails expressing Achilles-Hes7 was performed. D Representative kymographs of control and Aphidicolin-treated samples. E Quantification of PSM length by determining the size of the oscillating field (Line: mean, shading: standard deviation). Length normalized to the PSM length at experiment start. n(DMSO) = 9, n(Aphidicolin) = 11? F After 23 hr of incubation, tails were fixed and HCR against Hes7 and Uncx4.1 as well as counterstaining with DAPI were performed. Representative images are shown (same as in Fig. S14J). G-J After 23 hr of incubation, tails were fixed and stained with DAPI. G Representative images are shown. H-J Quantification of PSM length from tail tip to last formed somite boundary ( H ), somite length ( I ) and the ratio of somite length to PSM length as a measure of scaling ( J ). K Quantification of cell motility in fluorescence real-time imaging data of embryonic tails expressing Achilles-Hes7 (data corresponds to D,E). L Schematic model of how coupling of cell proliferation to segmentation clock affects somitogenesis.
Lb Thermofisher Waltham Massachusetts, supplied by Thermo Fisher, 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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aspergillus fumigatus isolates  (ATCC)
93
ATCC aspergillus fumigatus isolates
E10.5 embryonic tails were cultured ex vivo and treated with DMSO or the cell cycle inhibitor <t>Aphidicolin.</t> A-C After 23 hr of incubation, tails were fixed and stained for Brachyury and counterstained with DAPI. Scale bar 100 µm. A Representative images. B Quantification of the Brachyury signal along the AP axis of the PSM. Signal was normalized between 0 and 1. n(DMSO) = 6, n(Aphidicolin) = 11. C Quantification of the length of Brachyury gradient (Line: mean, shading: standard deviation). Intensity normalized between 0 and 1. * < 0.05; *** < 0.001; **** <0.0001. D,E Fluorescence real-time imaging of embryonic tails expressing Achilles-Hes7 was performed. D Representative kymographs of control and Aphidicolin-treated samples. E Quantification of PSM length by determining the size of the oscillating field (Line: mean, shading: standard deviation). Length normalized to the PSM length at experiment start. n(DMSO) = 9, n(Aphidicolin) = 11? F After 23 hr of incubation, tails were fixed and HCR against Hes7 and Uncx4.1 as well as counterstaining with DAPI were performed. Representative images are shown (same as in Fig. S14J). G-J After 23 hr of incubation, tails were fixed and stained with DAPI. G Representative images are shown. H-J Quantification of PSM length from tail tip to last formed somite boundary ( H ), somite length ( I ) and the ratio of somite length to PSM length as a measure of scaling ( J ). K Quantification of cell motility in fluorescence real-time imaging data of embryonic tails expressing Achilles-Hes7 (data corresponds to D,E). L Schematic model of how coupling of cell proliferation to segmentation clock affects somitogenesis.
Aspergillus Fumigatus Isolates, 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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g 46455 type  (ATCC)
93
ATCC g 46455 type
E10.5 embryonic tails were cultured ex vivo and treated with DMSO or the cell cycle inhibitor <t>Aphidicolin.</t> A-C After 23 hr of incubation, tails were fixed and stained for Brachyury and counterstained with DAPI. Scale bar 100 µm. A Representative images. B Quantification of the Brachyury signal along the AP axis of the PSM. Signal was normalized between 0 and 1. n(DMSO) = 6, n(Aphidicolin) = 11. C Quantification of the length of Brachyury gradient (Line: mean, shading: standard deviation). Intensity normalized between 0 and 1. * < 0.05; *** < 0.001; **** <0.0001. D,E Fluorescence real-time imaging of embryonic tails expressing Achilles-Hes7 was performed. D Representative kymographs of control and Aphidicolin-treated samples. E Quantification of PSM length by determining the size of the oscillating field (Line: mean, shading: standard deviation). Length normalized to the PSM length at experiment start. n(DMSO) = 9, n(Aphidicolin) = 11? F After 23 hr of incubation, tails were fixed and HCR against Hes7 and Uncx4.1 as well as counterstaining with DAPI were performed. Representative images are shown (same as in Fig. S14J). G-J After 23 hr of incubation, tails were fixed and stained with DAPI. G Representative images are shown. H-J Quantification of PSM length from tail tip to last formed somite boundary ( H ), somite length ( I ) and the ratio of somite length to PSM length as a measure of scaling ( J ). K Quantification of cell motility in fluorescence real-time imaging data of embryonic tails expressing Achilles-Hes7 (data corresponds to D,E). L Schematic model of how coupling of cell proliferation to segmentation clock affects somitogenesis.
G 46455 Type, 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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type translated sequence salpingoeca urceolata atcc 50560 m 46455  (ATCC)
90
ATCC type translated sequence salpingoeca urceolata atcc 50560 m 46455
E10.5 embryonic tails were cultured ex vivo and treated with DMSO or the cell cycle inhibitor <t>Aphidicolin.</t> A-C After 23 hr of incubation, tails were fixed and stained for Brachyury and counterstained with DAPI. Scale bar 100 µm. A Representative images. B Quantification of the Brachyury signal along the AP axis of the PSM. Signal was normalized between 0 and 1. n(DMSO) = 6, n(Aphidicolin) = 11. C Quantification of the length of Brachyury gradient (Line: mean, shading: standard deviation). Intensity normalized between 0 and 1. * < 0.05; *** < 0.001; **** <0.0001. D,E Fluorescence real-time imaging of embryonic tails expressing Achilles-Hes7 was performed. D Representative kymographs of control and Aphidicolin-treated samples. E Quantification of PSM length by determining the size of the oscillating field (Line: mean, shading: standard deviation). Length normalized to the PSM length at experiment start. n(DMSO) = 9, n(Aphidicolin) = 11? F After 23 hr of incubation, tails were fixed and HCR against Hes7 and Uncx4.1 as well as counterstaining with DAPI were performed. Representative images are shown (same as in Fig. S14J). G-J After 23 hr of incubation, tails were fixed and stained with DAPI. G Representative images are shown. H-J Quantification of PSM length from tail tip to last formed somite boundary ( H ), somite length ( I ) and the ratio of somite length to PSM length as a measure of scaling ( J ). K Quantification of cell motility in fluorescence real-time imaging data of embryonic tails expressing Achilles-Hes7 (data corresponds to D,E). L Schematic model of how coupling of cell proliferation to segmentation clock affects somitogenesis.
Type Translated Sequence Salpingoeca Urceolata Atcc 50560 M 46455, supplied by ATCC, 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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type translated sequence salpingoeca urceolata atcc 50560 m 46455 - by Bioz Stars, 2026-02
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bye broth  (Thermo Fisher)
94
Thermo Fisher bye broth
E10.5 embryonic tails were cultured ex vivo and treated with DMSO or the cell cycle inhibitor <t>Aphidicolin.</t> A-C After 23 hr of incubation, tails were fixed and stained for Brachyury and counterstained with DAPI. Scale bar 100 µm. A Representative images. B Quantification of the Brachyury signal along the AP axis of the PSM. Signal was normalized between 0 and 1. n(DMSO) = 6, n(Aphidicolin) = 11. C Quantification of the length of Brachyury gradient (Line: mean, shading: standard deviation). Intensity normalized between 0 and 1. * < 0.05; *** < 0.001; **** <0.0001. D,E Fluorescence real-time imaging of embryonic tails expressing Achilles-Hes7 was performed. D Representative kymographs of control and Aphidicolin-treated samples. E Quantification of PSM length by determining the size of the oscillating field (Line: mean, shading: standard deviation). Length normalized to the PSM length at experiment start. n(DMSO) = 9, n(Aphidicolin) = 11? F After 23 hr of incubation, tails were fixed and HCR against Hes7 and Uncx4.1 as well as counterstaining with DAPI were performed. Representative images are shown (same as in Fig. S14J). G-J After 23 hr of incubation, tails were fixed and stained with DAPI. G Representative images are shown. H-J Quantification of PSM length from tail tip to last formed somite boundary ( H ), somite length ( I ) and the ratio of somite length to PSM length as a measure of scaling ( J ). K Quantification of cell motility in fluorescence real-time imaging data of embryonic tails expressing Achilles-Hes7 (data corresponds to D,E). L Schematic model of how coupling of cell proliferation to segmentation clock affects somitogenesis.
Bye Broth, supplied by Thermo Fisher, 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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Average 94 stars, based on 1 article reviews
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Strains used in fermentation.

Journal: Current Research in Food Science

Article Title: Modulating the aroma and taste profile of soybean using novel strains for fermentation

doi: 10.1016/j.crfs.2024.100933

Figure Lengend Snippet: Strains used in fermentation.

Article Snippet: PN , , Penicillium nalgiovense , ATCC 46455.

Techniques: Bacteria

E10.5 embryonic tails were cultured ex vivo and treated with DMSO or the cell cycle inhibitor Aphidicolin. A-C After 23 hr of incubation, tails were fixed and stained for Brachyury and counterstained with DAPI. Scale bar 100 µm. A Representative images. B Quantification of the Brachyury signal along the AP axis of the PSM. Signal was normalized between 0 and 1. n(DMSO) = 6, n(Aphidicolin) = 11. C Quantification of the length of Brachyury gradient (Line: mean, shading: standard deviation). Intensity normalized between 0 and 1. * < 0.05; *** < 0.001; **** <0.0001. D,E Fluorescence real-time imaging of embryonic tails expressing Achilles-Hes7 was performed. D Representative kymographs of control and Aphidicolin-treated samples. E Quantification of PSM length by determining the size of the oscillating field (Line: mean, shading: standard deviation). Length normalized to the PSM length at experiment start. n(DMSO) = 9, n(Aphidicolin) = 11? F After 23 hr of incubation, tails were fixed and HCR against Hes7 and Uncx4.1 as well as counterstaining with DAPI were performed. Representative images are shown (same as in Fig. S14J). G-J After 23 hr of incubation, tails were fixed and stained with DAPI. G Representative images are shown. H-J Quantification of PSM length from tail tip to last formed somite boundary ( H ), somite length ( I ) and the ratio of somite length to PSM length as a measure of scaling ( J ). K Quantification of cell motility in fluorescence real-time imaging data of embryonic tails expressing Achilles-Hes7 (data corresponds to D,E). L Schematic model of how coupling of cell proliferation to segmentation clock affects somitogenesis.

Journal: bioRxiv

Article Title: Scaling of mouse somitogenesis by coupling of cell cycle to segmentation clock oscillations

doi: 10.1101/2025.01.10.632257

Figure Lengend Snippet: E10.5 embryonic tails were cultured ex vivo and treated with DMSO or the cell cycle inhibitor Aphidicolin. A-C After 23 hr of incubation, tails were fixed and stained for Brachyury and counterstained with DAPI. Scale bar 100 µm. A Representative images. B Quantification of the Brachyury signal along the AP axis of the PSM. Signal was normalized between 0 and 1. n(DMSO) = 6, n(Aphidicolin) = 11. C Quantification of the length of Brachyury gradient (Line: mean, shading: standard deviation). Intensity normalized between 0 and 1. * < 0.05; *** < 0.001; **** <0.0001. D,E Fluorescence real-time imaging of embryonic tails expressing Achilles-Hes7 was performed. D Representative kymographs of control and Aphidicolin-treated samples. E Quantification of PSM length by determining the size of the oscillating field (Line: mean, shading: standard deviation). Length normalized to the PSM length at experiment start. n(DMSO) = 9, n(Aphidicolin) = 11? F After 23 hr of incubation, tails were fixed and HCR against Hes7 and Uncx4.1 as well as counterstaining with DAPI were performed. Representative images are shown (same as in Fig. S14J). G-J After 23 hr of incubation, tails were fixed and stained with DAPI. G Representative images are shown. H-J Quantification of PSM length from tail tip to last formed somite boundary ( H ), somite length ( I ) and the ratio of somite length to PSM length as a measure of scaling ( J ). K Quantification of cell motility in fluorescence real-time imaging data of embryonic tails expressing Achilles-Hes7 (data corresponds to D,E). L Schematic model of how coupling of cell proliferation to segmentation clock affects somitogenesis.

Article Snippet: For perturbation experiments on whole mount and spread-out tail tips, the following compounds were used: CHIR99021 (Chiron, Sigma-Aldrich, SML1046) at 10 µM, IWP-2 (Sigma-Aldrich, I0536) at 1 µM, Aphidicolin (ThermoFisher, J60236.MCR) at 1.6 µg/mL, Thymidine (Sigma-Aldrich, T9250) at 2 mM, Palbociclib (Selleckchem, PD-0332991) at 1 µM, and RO-3306 (Sigma-Aldrich, 217699) at 10 µM.

Techniques: Cell Culture, Ex Vivo, Incubation, Staining, Standard Deviation, Fluorescence, Imaging, Expressing, Control