prolongtm gold antifade 9 mountant with dapi (Thermo Fisher)
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prolongtm gold antifade 9 mountant with dapi
Prolongtm Gold Antifade 9 Mountant With Dapi, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/prolongtm+gold+antifade+9+mountant+with+dapi/AGAR+1KG+1KG/pm40929079-86-23-30
Average 97 stars, based on 1 article reviews
Prolongtm Gold Antifade 9 Mountant With Dapi, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/prolongtm+gold+antifade+9+mountant+with+dapi/AGAR+1KG+1KG/pm40929079-86-23-30
Average 97 stars, based on 1 article reviews
prolongtm gold antifade 9 mountant with dapi - by Bioz Stars,
2026-10
97/100 stars
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Microscopy:Article Title: Preclinical and first-in-human evidence of 4-hydroxybenzoic acid for mitochondrial COQ2 deficiency. Article Snippet: 2 To identify neurons (NeuN, 1:300, Merck Millipore), myelin (anti-MBP, 1:500, Abcam), 3 astrocytes (GFAP, 1:500, Sigma Aldrich) and microglial activation (Iba1, 1:500, Wako), 4 immunohistochemistry was performed.17 Briefly, after deparaffinization, sections were boiled 5 using 0.1 M sodium citrate buffer (pH 6) at 90°C for 40 min. After several washes in phosphate-6 buffered saline (PBS, 0.1 M, 0.02% Triton X-100), sections were incubated with the primary 7 antibody at 4°C overnight. .. Secondary antibodies conjugated with Alexa Fluor 488 or 594 were 8 then applied at 37°C for 2 h. Finally, slides were mounted with Software:Article Title: Preclinical and first-in-human evidence of 4-hydroxybenzoic acid for mitochondrial COQ2 deficiency. Article Snippet: 2 To identify neurons (NeuN, 1:300, Merck Millipore), myelin (anti-MBP, 1:500, Abcam), 3 astrocytes (GFAP, 1:500, Sigma Aldrich) and microglial activation (Iba1, 1:500, Wako), 4 immunohistochemistry was performed.17 Briefly, after deparaffinization, sections were boiled 5 using 0.1 M sodium citrate buffer (pH 6) at 90°C for 40 min. After several washes in phosphate-6 buffered saline (PBS, 0.1 M, 0.02% Triton X-100), sections were incubated with the primary 7 antibody at 4°C overnight. .. Secondary antibodies conjugated with Alexa Fluor 488 or 594 were 8 then applied at 37°C for 2 h. Finally, slides were mounted with |