tubes 14 × 89 mm open top thinwall ultraclear tubes (Danaher Inc)
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Danaher Inc
tubes 14 × 89 mm open top thinwall ultraclear tubes
Tubes 14 × 89 Mm Open Top Thinwall Ultraclear Tubes, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/tubes+14+%C3%97+89+mm+open+top+thinwall+ultraclear+tubes/pm39038807-178-79-88
Average 86 stars, based on 1 article reviews
Tubes 14 × 89 Mm Open Top Thinwall Ultraclear Tubes, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/tubes+14+%C3%97+89+mm+open+top+thinwall+ultraclear+tubes/pm39038807-178-79-88
Average 86 stars, based on 1 article reviews
tubes 14 × 89 mm open top thinwall ultraclear tubes - by Bioz Stars,
2026-10
86/100 stars
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Concentration Assay:Article Title: Functional Modification of Cyanobacterial Phycobiliprotein and Phycobilisomes through Bilin Metabolism Control. Article Snippet: The cells were washed twice in 0.6 M KP buffer and resuspended in 0.6 mL of 0.6 M KP buffer, after which they were lysed by vortexing with glass beads, and the PBS complexes were extracted from the thylakoid membranes by vortexing with Triton X-100 (final concentration = 2%) for 15 min. After centrifugation (20,000 × g, 20 min, 18 °C), 200 μL of supernatant was loaded onto sucrose gradients (10−50% sucrose in 0.6 M KP buffer) prepared in Centrifugation:Article Title: Functional Modification of Cyanobacterial Phycobiliprotein and Phycobilisomes through Bilin Metabolism Control. Article Snippet: The cells were washed twice in 0.6 M KP buffer and resuspended in 0.6 mL of 0.6 M KP buffer, after which they were lysed by vortexing with glass beads, and the PBS complexes were extracted from the thylakoid membranes by vortexing with Triton X-100 (final concentration = 2%) for 15 min. After centrifugation (20,000 × g, 20 min, 18 °C), 200 μL of supernatant was loaded onto sucrose gradients (10−50% sucrose in 0.6 M KP buffer) prepared in |