image studio software version 6 1 (LI-COR)
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image studio software version 6 1
Image Studio Software Version 6 1, supplied by LI-COR, used in various techniques. Bioz Stars score: 98/100, based on 397 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/image+studio+software+version+6+1/Odyssey+Fc+Image+Studio+Analysis+Software+-+Plate+and+Grid+Analysis+Add-On/pm40846110-277-67-72
Average 98 stars, based on 397 article reviews
Image Studio Software Version 6 1, supplied by LI-COR, used in various techniques. Bioz Stars score: 98/100, based on 397 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/image+studio+software+version+6+1/Odyssey+Fc+Image+Studio+Analysis+Software+-+Plate+and+Grid+Analysis+Add-On/pm40846110-277-67-72
Average 98 stars, based on 397 article reviews
image studio software version 6 1 - by Bioz Stars,
2026-10
98/100 stars
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Related Articles
Membrane:Article Title: Loss of col4a1 in zebrafish recapitulates the cerebrovascular phenotypes associated with monogenic cerebral small vessel disease. Article Snippet: Resolved gels were transferred onto a nitrocellulose blotting membrane using the XCell II Blot module system (Invitrogen) at 30 V for 90 min. Membranes were blocked in 5 % milk in PBS for 30 min at room temperature, washed with PBST and incubated overnight with anti-Collagen IV antibody (Abcam, ab6586, diluted 1:500) and anti-γ-tubulin (Merck, T6557, diluted 1:1000) in 5 % milk PBST. .. The membrane was washed in PBST and incubated for 60 min at room temperature with secondary antibodies, anti-Rabbit IgG DyLightTM 800 (SA5–35,571, Cell Signalling Technologies) and anti-Mouse IgG Alexa FluorTM 680 (A-21,058, Invitrogen); both diluted in 1:10,000 in 5 % PBST before a final PBST wash. Proteins were then visualised with Odyssey CLx Imager (LICORbio) using channels 700 and 800 and quantification of bands was performed in Incubation:Article Title: Loss of col4a1 in zebrafish recapitulates the cerebrovascular phenotypes associated with monogenic cerebral small vessel disease. Article Snippet: Resolved gels were transferred onto a nitrocellulose blotting membrane using the XCell II Blot module system (Invitrogen) at 30 V for 90 min. Membranes were blocked in 5 % milk in PBS for 30 min at room temperature, washed with PBST and incubated overnight with anti-Collagen IV antibody (Abcam, ab6586, diluted 1:500) and anti-γ-tubulin (Merck, T6557, diluted 1:1000) in 5 % milk PBST. .. The membrane was washed in PBST and incubated for 60 min at room temperature with secondary antibodies, anti-Rabbit IgG DyLightTM 800 (SA5–35,571, Cell Signalling Technologies) and anti-Mouse IgG Alexa FluorTM 680 (A-21,058, Invitrogen); both diluted in 1:10,000 in 5 % PBST before a final PBST wash. Proteins were then visualised with Odyssey CLx Imager (LICORbio) using channels 700 and 800 and quantification of bands was performed in Software:Article Title: Loss of col4a1 in zebrafish recapitulates the cerebrovascular phenotypes associated with monogenic cerebral small vessel disease. Article Snippet: Resolved gels were transferred onto a nitrocellulose blotting membrane using the XCell II Blot module system (Invitrogen) at 30 V for 90 min. Membranes were blocked in 5 % milk in PBS for 30 min at room temperature, washed with PBST and incubated overnight with anti-Collagen IV antibody (Abcam, ab6586, diluted 1:500) and anti-γ-tubulin (Merck, T6557, diluted 1:1000) in 5 % milk PBST. .. The membrane was washed in PBST and incubated for 60 min at room temperature with secondary antibodies, anti-Rabbit IgG DyLightTM 800 (SA5–35,571, Cell Signalling Technologies) and anti-Mouse IgG Alexa FluorTM 680 (A-21,058, Invitrogen); both diluted in 1:10,000 in 5 % PBST before a final PBST wash. Proteins were then visualised with Odyssey CLx Imager (LICORbio) using channels 700 and 800 and quantification of bands was performed in |