fluorescent dye reddot 2 Search Results


fluorescent dye  (Biotium)
95
Biotium fluorescent dye
Fluorescent Dye, supplied by Biotium, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fluorescent+dye+reddot+2/RedDot2/pmc09217854-112-19-21
Average 95 stars, based on 1 article reviews
fluorescent dye - by Bioz Stars, 2026-10
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odyssey  (LI-COR)
99
LI-COR odyssey
Odyssey, supplied by LI-COR, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fluorescent+dye+reddot+2/Odyssey/custom%40Odyssey%4023853582
Average 99 stars, based on 1 article reviews
odyssey - by Bioz Stars, 2026-10
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odyssey imaging system  (LI-COR)
99
LI-COR odyssey imaging system
Odyssey Imaging System, supplied by LI-COR, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fluorescent+dye+reddot+2/Odyssey+Imaging+System/custom%40odyssey-imaging-system%4023853582
Average 99 stars, based on 1 article reviews
odyssey imaging system - by Bioz Stars, 2026-10
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reddot2  (IDEX)
90
IDEX reddot2
Whole-brain analysis of input cell populations projecting to ARH Kiss1+ neurons (A) Virus injection scheme. AAV carrying mCherry, TVA receptor, and optimized glycoprotein (oG) was injected into the ARH of Kiss1-Cre transgenic mouse, followed by injection of modified rabies virus carrying GFP. Cells expressing both mCherry and GFP are the starter cells. (B) Quantification of starter cell localization. The ratio was computed by dividing the cell count in each region by the total number of starter cells. The total number of starter cells in each sample is shown on the right end of the heatmap. (C) Whole-brain view of all input cells. (D) Total cell count and the distribution of input cells. Only male brains were considered here. (E) Cell-density heatmap of all brain regions (excluding the isocortex and cerebellum, where virtually no input cells were detected). The means of male and female brains are shown. (F) The plot shows extremely sparse input cell populations in previously unidentified brain regions (n = 3). Only male brains were considered here. Data are shown and mean ± SD (n = 3). (G) Raw GFP (black) and nuclear staining <t>(RedDot2,</t> purple) images showing the regions identified in (F). Macro views (top) and zoomed-in views (of boxed areas; bottom) are shown. Brain region acronyms follow the ontology defined by the Allen Brain Atlas.
Reddot2, supplied by IDEX, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fluorescent+dye+reddot+2/reddot2/pmc09017177-457-46-54
Average 90 stars, based on 1 article reviews
reddot2 - by Bioz Stars, 2026-10
90/100 stars
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gfp  (IDEX)
90
IDEX gfp
Whole-brain analysis of input cell populations projecting to ARH Kiss1+ neurons (A) Virus injection scheme. AAV carrying mCherry, TVA receptor, and optimized glycoprotein (oG) was injected into the ARH of Kiss1-Cre transgenic mouse, followed by injection of modified rabies virus carrying <t>GFP.</t> Cells expressing both mCherry and GFP are the starter cells. (B) Quantification of starter cell localization. The ratio was computed by dividing the cell count in each region by the total number of starter cells. The total number of starter cells in each sample is shown on the right end of the heatmap. (C) Whole-brain view of all input cells. (D) Total cell count and the distribution of input cells. Only male brains were considered here. (E) Cell-density heatmap of all brain regions (excluding the isocortex and cerebellum, where virtually no input cells were detected). The means of male and female brains are shown. (F) The plot shows extremely sparse input cell populations in previously unidentified brain regions (n = 3). Only male brains were considered here. Data are shown and mean ± SD (n = 3). (G) Raw GFP (black) and nuclear <t>staining</t> <t>(RedDot2,</t> purple) images showing the regions identified in (F). Macro views (top) and zoomed-in views (of boxed areas; bottom) are shown. Brain region acronyms follow the ontology defined by the Allen Brain Atlas.
Gfp, supplied by IDEX, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fluorescent+dye+reddot+2/bandpass+filter/pmc09017177-457-36-45
Average 90 stars, based on 1 article reviews
gfp - by Bioz Stars, 2026-10
90/100 stars
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Image Search Results


Whole-brain analysis of input cell populations projecting to ARH Kiss1+ neurons (A) Virus injection scheme. AAV carrying mCherry, TVA receptor, and optimized glycoprotein (oG) was injected into the ARH of Kiss1-Cre transgenic mouse, followed by injection of modified rabies virus carrying GFP. Cells expressing both mCherry and GFP are the starter cells. (B) Quantification of starter cell localization. The ratio was computed by dividing the cell count in each region by the total number of starter cells. The total number of starter cells in each sample is shown on the right end of the heatmap. (C) Whole-brain view of all input cells. (D) Total cell count and the distribution of input cells. Only male brains were considered here. (E) Cell-density heatmap of all brain regions (excluding the isocortex and cerebellum, where virtually no input cells were detected). The means of male and female brains are shown. (F) The plot shows extremely sparse input cell populations in previously unidentified brain regions (n = 3). Only male brains were considered here. Data are shown and mean ± SD (n = 3). (G) Raw GFP (black) and nuclear staining (RedDot2, purple) images showing the regions identified in (F). Macro views (top) and zoomed-in views (of boxed areas; bottom) are shown. Brain region acronyms follow the ontology defined by the Allen Brain Atlas.

Journal: Cell Reports Methods

Article Title: CUBIC-Cloud provides an integrative computational framework toward community-driven whole-mouse-brain mapping

doi: 10.1016/j.crmeth.2021.100038

Figure Lengend Snippet: Whole-brain analysis of input cell populations projecting to ARH Kiss1+ neurons (A) Virus injection scheme. AAV carrying mCherry, TVA receptor, and optimized glycoprotein (oG) was injected into the ARH of Kiss1-Cre transgenic mouse, followed by injection of modified rabies virus carrying GFP. Cells expressing both mCherry and GFP are the starter cells. (B) Quantification of starter cell localization. The ratio was computed by dividing the cell count in each region by the total number of starter cells. The total number of starter cells in each sample is shown on the right end of the heatmap. (C) Whole-brain view of all input cells. (D) Total cell count and the distribution of input cells. Only male brains were considered here. (E) Cell-density heatmap of all brain regions (excluding the isocortex and cerebellum, where virtually no input cells were detected). The means of male and female brains are shown. (F) The plot shows extremely sparse input cell populations in previously unidentified brain regions (n = 3). Only male brains were considered here. Data are shown and mean ± SD (n = 3). (G) Raw GFP (black) and nuclear staining (RedDot2, purple) images showing the regions identified in (F). Macro views (top) and zoomed-in views (of boxed areas; bottom) are shown. Brain region acronyms follow the ontology defined by the Allen Brain Atlas.

Article Snippet: For each dye/FP, the following laser and fluorescence filter pair was used: Alexa 594 [Ex: 594 nm, Em: 641/75 nm bandpass (FF02-641/75-32, Semrock)], Cy3 [Ex: 532 nm, Em: 585/40 nm bandpass (FF01-585/40-32, Semrock)], SYTOX-G, BOBO-1 and GFP [Ex: 488 nm, Em: 520/40 nm bandpass (FF01-520/44-32, Semrock)], RedDot2 [Ex: 642nm, Em: 708/75 nm bandpass (FF01-708/75-32, Semrock)], mCherry [Ex: 594 nm, Em: 628/32 nm bandpass (FF01-628/32-32, Semrock)].

Techniques: Injection, Transgenic Assay, Modification, Expressing, Cell Counting, Staining

Whole-brain analysis of input cell populations projecting to ARH Kiss1+ neurons (A) Virus injection scheme. AAV carrying mCherry, TVA receptor, and optimized glycoprotein (oG) was injected into the ARH of Kiss1-Cre transgenic mouse, followed by injection of modified rabies virus carrying GFP. Cells expressing both mCherry and GFP are the starter cells. (B) Quantification of starter cell localization. The ratio was computed by dividing the cell count in each region by the total number of starter cells. The total number of starter cells in each sample is shown on the right end of the heatmap. (C) Whole-brain view of all input cells. (D) Total cell count and the distribution of input cells. Only male brains were considered here. (E) Cell-density heatmap of all brain regions (excluding the isocortex and cerebellum, where virtually no input cells were detected). The means of male and female brains are shown. (F) The plot shows extremely sparse input cell populations in previously unidentified brain regions (n = 3). Only male brains were considered here. Data are shown and mean ± SD (n = 3). (G) Raw GFP (black) and nuclear staining (RedDot2, purple) images showing the regions identified in (F). Macro views (top) and zoomed-in views (of boxed areas; bottom) are shown. Brain region acronyms follow the ontology defined by the Allen Brain Atlas.

Journal: Cell Reports Methods

Article Title: CUBIC-Cloud provides an integrative computational framework toward community-driven whole-mouse-brain mapping

doi: 10.1016/j.crmeth.2021.100038

Figure Lengend Snippet: Whole-brain analysis of input cell populations projecting to ARH Kiss1+ neurons (A) Virus injection scheme. AAV carrying mCherry, TVA receptor, and optimized glycoprotein (oG) was injected into the ARH of Kiss1-Cre transgenic mouse, followed by injection of modified rabies virus carrying GFP. Cells expressing both mCherry and GFP are the starter cells. (B) Quantification of starter cell localization. The ratio was computed by dividing the cell count in each region by the total number of starter cells. The total number of starter cells in each sample is shown on the right end of the heatmap. (C) Whole-brain view of all input cells. (D) Total cell count and the distribution of input cells. Only male brains were considered here. (E) Cell-density heatmap of all brain regions (excluding the isocortex and cerebellum, where virtually no input cells were detected). The means of male and female brains are shown. (F) The plot shows extremely sparse input cell populations in previously unidentified brain regions (n = 3). Only male brains were considered here. Data are shown and mean ± SD (n = 3). (G) Raw GFP (black) and nuclear staining (RedDot2, purple) images showing the regions identified in (F). Macro views (top) and zoomed-in views (of boxed areas; bottom) are shown. Brain region acronyms follow the ontology defined by the Allen Brain Atlas.

Article Snippet: For each dye/FP, the following laser and fluorescence filter pair was used: Alexa 594 [Ex: 594 nm, Em: 641/75 nm bandpass (FF02-641/75-32, Semrock)], Cy3 [Ex: 532 nm, Em: 585/40 nm bandpass (FF01-585/40-32, Semrock)], SYTOX-G, BOBO-1 and GFP [Ex: 488 nm, Em: 520/40 nm bandpass (FF01-520/44-32, Semrock)], RedDot2 [Ex: 642nm, Em: 708/75 nm bandpass (FF01-708/75-32, Semrock)], mCherry [Ex: 594 nm, Em: 628/32 nm bandpass (FF01-628/32-32, Semrock)].

Techniques: Injection, Transgenic Assay, Modification, Expressing, Cell Counting, Staining