chip fluorescence scanner (CapitalBio Corporation)
90
Structured Review
CapitalBio Corporation
chip fluorescence scanner
Chip Fluorescence Scanner, supplied by CapitalBio Corporation, 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/chip+fluorescence+scanner/chip+fluorescence+scanner/pmc07919521-149-60-63
Average 90 stars, based on 1 article reviews
Chip Fluorescence Scanner, supplied by CapitalBio Corporation, 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/chip+fluorescence+scanner/chip+fluorescence+scanner/pmc07919521-149-60-63
Average 90 stars, based on 1 article reviews
chip fluorescence scanner - by Bioz Stars,
2026-09
90/100 stars
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Microarray:Article Title: The study of antiviral drugs targeting SARS-CoV-2 nucleocapsid and spike proteins through large-scale compound repurposing Article Snippet: Briefly, the printed microarray (stored at -80 °C) was immersed in blocking solution (3 mL 10% BSA with 7 mL PBS); the mixture was shaken by a side-swing shaker for an hour at room conditions; ultrapure water was then used to clean the chip; after drying in a chip dryer, the chip was scanned at 635 nm by using the chip fluorescence scanner (CapitalBio,= http://www.capitalbiotech.com/about.html?categoryId=28 Luxscan TM 10K-A). .. After the collection of the background signals, the printed microarray was cleaned with ultrapure water and then immersed in blocking solution (3 mL 10% BSA, 7 mL 1×PBS); the chip was then placed face up in the well of a 4-well rectangular Petri dish; 3 mL of Cy5 labeled protein solution was gently added into the slide bar code sticker and diffused over the chip; lidded the plate and placed the mixture on a shaking platform, allowing the solution to stir gently over the surface of the slide; after incubation with protein, the chip was cleaned in PBST (Phosphate Buffered Saline with 0.05% Tween 20) three times (5 min/time) at room conditions, following by ultrapure water (2 times 5 min/time); the cleaned chip was then centrifuged to dry and scanned at 635 nm by using the Article Title: The study of antiviral drugs targeting SARS-CoV-2 nucleocapsid and spike proteins through large-scale compound repurposing Article Snippet: .. Briefly, the printed microarray (stored at -80 °C) was immersed in blocking solution (3 mL 10% BSA with 7 mL PBS); the mixture was shaken by a side-swing shaker for an hour at room conditions; ultrapure water was then used to clean the chip; after drying in a chip dryer, the chip was scanned at 635 nm by using the Blocking Assay:Article Title: The study of antiviral drugs targeting SARS-CoV-2 nucleocapsid and spike proteins through large-scale compound repurposing Article Snippet: Briefly, the printed microarray (stored at -80 °C) was immersed in blocking solution (3 mL 10% BSA with 7 mL PBS); the mixture was shaken by a side-swing shaker for an hour at room conditions; ultrapure water was then used to clean the chip; after drying in a chip dryer, the chip was scanned at 635 nm by using the chip fluorescence scanner (CapitalBio,= http://www.capitalbiotech.com/about.html?categoryId=28 Luxscan TM 10K-A). .. After the collection of the background signals, the printed microarray was cleaned with ultrapure water and then immersed in blocking solution (3 mL 10% BSA, 7 mL 1×PBS); the chip was then placed face up in the well of a 4-well rectangular Petri dish; 3 mL of Cy5 labeled protein solution was gently added into the slide bar code sticker and diffused over the chip; lidded the plate and placed the mixture on a shaking platform, allowing the solution to stir gently over the surface of the slide; after incubation with protein, the chip was cleaned in PBST (Phosphate Buffered Saline with 0.05% Tween 20) three times (5 min/time) at room conditions, following by ultrapure water (2 times 5 min/time); the cleaned chip was then centrifuged to dry and scanned at 635 nm by using the Article Title: The study of antiviral drugs targeting SARS-CoV-2 nucleocapsid and spike proteins through large-scale compound repurposing Article Snippet: .. Briefly, the printed microarray (stored at -80 °C) was immersed in blocking solution (3 mL 10% BSA with 7 mL PBS); the mixture was shaken by a side-swing shaker for an hour at room conditions; ultrapure water was then used to clean the chip; after drying in a chip dryer, the chip was scanned at 635 nm by using the Labeling:Article Title: The study of antiviral drugs targeting SARS-CoV-2 nucleocapsid and spike proteins through large-scale compound repurposing Article Snippet: Briefly, the printed microarray (stored at -80 °C) was immersed in blocking solution (3 mL 10% BSA with 7 mL PBS); the mixture was shaken by a side-swing shaker for an hour at room conditions; ultrapure water was then used to clean the chip; after drying in a chip dryer, the chip was scanned at 635 nm by using the chip fluorescence scanner (CapitalBio,= http://www.capitalbiotech.com/about.html?categoryId=28 Luxscan TM 10K-A). .. After the collection of the background signals, the printed microarray was cleaned with ultrapure water and then immersed in blocking solution (3 mL 10% BSA, 7 mL 1×PBS); the chip was then placed face up in the well of a 4-well rectangular Petri dish; 3 mL of Cy5 labeled protein solution was gently added into the slide bar code sticker and diffused over the chip; lidded the plate and placed the mixture on a shaking platform, allowing the solution to stir gently over the surface of the slide; after incubation with protein, the chip was cleaned in PBST (Phosphate Buffered Saline with 0.05% Tween 20) three times (5 min/time) at room conditions, following by ultrapure water (2 times 5 min/time); the cleaned chip was then centrifuged to dry and scanned at 635 nm by using the Incubation:Article Title: The study of antiviral drugs targeting SARS-CoV-2 nucleocapsid and spike proteins through large-scale compound repurposing Article Snippet: Briefly, the printed microarray (stored at -80 °C) was immersed in blocking solution (3 mL 10% BSA with 7 mL PBS); the mixture was shaken by a side-swing shaker for an hour at room conditions; ultrapure water was then used to clean the chip; after drying in a chip dryer, the chip was scanned at 635 nm by using the chip fluorescence scanner (CapitalBio,= http://www.capitalbiotech.com/about.html?categoryId=28 Luxscan TM 10K-A). .. After the collection of the background signals, the printed microarray was cleaned with ultrapure water and then immersed in blocking solution (3 mL 10% BSA, 7 mL 1×PBS); the chip was then placed face up in the well of a 4-well rectangular Petri dish; 3 mL of Cy5 labeled protein solution was gently added into the slide bar code sticker and diffused over the chip; lidded the plate and placed the mixture on a shaking platform, allowing the solution to stir gently over the surface of the slide; after incubation with protein, the chip was cleaned in PBST (Phosphate Buffered Saline with 0.05% Tween 20) three times (5 min/time) at room conditions, following by ultrapure water (2 times 5 min/time); the cleaned chip was then centrifuged to dry and scanned at 635 nm by using the Fluorescence:Article Title: The study of antiviral drugs targeting SARS-CoV-2 nucleocapsid and spike proteins through large-scale compound repurposing Article Snippet: Briefly, the printed microarray (stored at -80 °C) was immersed in blocking solution (3 mL 10% BSA with 7 mL PBS); the mixture was shaken by a side-swing shaker for an hour at room conditions; ultrapure water was then used to clean the chip; after drying in a chip dryer, the chip was scanned at 635 nm by using the chip fluorescence scanner (CapitalBio,= http://www.capitalbiotech.com/about.html?categoryId=28 Luxscan TM 10K-A). .. After the collection of the background signals, the printed microarray was cleaned with ultrapure water and then immersed in blocking solution (3 mL 10% BSA, 7 mL 1×PBS); the chip was then placed face up in the well of a 4-well rectangular Petri dish; 3 mL of Cy5 labeled protein solution was gently added into the slide bar code sticker and diffused over the chip; lidded the plate and placed the mixture on a shaking platform, allowing the solution to stir gently over the surface of the slide; after incubation with protein, the chip was cleaned in PBST (Phosphate Buffered Saline with 0.05% Tween 20) three times (5 min/time) at room conditions, following by ultrapure water (2 times 5 min/time); the cleaned chip was then centrifuged to dry and scanned at 635 nm by using the Article Title: The study of antiviral drugs targeting SARS-CoV-2 nucleocapsid and spike proteins through large-scale compound repurposing Article Snippet: .. Briefly, the printed microarray (stored at -80 °C) was immersed in blocking solution (3 mL 10% BSA with 7 mL PBS); the mixture was shaken by a side-swing shaker for an hour at room conditions; ultrapure water was then used to clean the chip; after drying in a chip dryer, the chip was scanned at 635 nm by using the |