s2 cell pellets Search Results


s2 cell pellet  (Thermo Fisher)
99
Thermo Fisher s2 cell pellet
Multiplex imaging of TIM and CRY bands. (A) Lane 1-6 show TIM and CRY SWFTI signals on HA resin, whereas lane 7-9 show the signals in lysate samples. Lane 10-12 exhibit fluorescent signals from the internal standard CLIP-CRY-SNAP. To prevent fluorescence crosstalk, Lane 10 and 11 have the standard only mixed with CLIP dye, whereas lane 12 contains the standard with only SNAP dye. In lane 11 the standard was diluted to 10%. (B) The quantification of standard by purified SNAP proteins. The standard was diluted to 20% and mixed with SNAP dye.
S2 Cell Pellet, supplied by Thermo Fisher, 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/result/s2 cell pellet/product/Thermo Fisher
Average 99 stars, based on 1 article reviews
s2 cell pellet - by Bioz Stars, 2026-02
99/100 stars
  Buy from Supplier
terasaki park medium  (Thermo Fisher)
90
Thermo Fisher terasaki park medium
Multiplex imaging of TIM and CRY bands. (A) Lane 1-6 show TIM and CRY SWFTI signals on HA resin, whereas lane 7-9 show the signals in lysate samples. Lane 10-12 exhibit fluorescent signals from the internal standard CLIP-CRY-SNAP. To prevent fluorescence crosstalk, Lane 10 and 11 have the standard only mixed with CLIP dye, whereas lane 12 contains the standard with only SNAP dye. In lane 11 the standard was diluted to 10%. (B) The quantification of standard by purified SNAP proteins. The standard was diluted to 20% and mixed with SNAP dye.
Terasaki Park Medium, supplied by Thermo Fisher, 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/result/terasaki park medium/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
terasaki park medium - by Bioz Stars, 2026-02
90/100 stars
  Buy from Supplier

Image Search Results


Multiplex imaging of TIM and CRY bands. (A) Lane 1-6 show TIM and CRY SWFTI signals on HA resin, whereas lane 7-9 show the signals in lysate samples. Lane 10-12 exhibit fluorescent signals from the internal standard CLIP-CRY-SNAP. To prevent fluorescence crosstalk, Lane 10 and 11 have the standard only mixed with CLIP dye, whereas lane 12 contains the standard with only SNAP dye. In lane 11 the standard was diluted to 10%. (B) The quantification of standard by purified SNAP proteins. The standard was diluted to 20% and mixed with SNAP dye.

Journal: bioRxiv

Article Title: Mechanistic insight into light-dependent recognition of Timeless by Drosophila cryptochrome

doi: 10.1101/2021.09.10.459772

Figure Lengend Snippet: Multiplex imaging of TIM and CRY bands. (A) Lane 1-6 show TIM and CRY SWFTI signals on HA resin, whereas lane 7-9 show the signals in lysate samples. Lane 10-12 exhibit fluorescent signals from the internal standard CLIP-CRY-SNAP. To prevent fluorescence crosstalk, Lane 10 and 11 have the standard only mixed with CLIP dye, whereas lane 12 contains the standard with only SNAP dye. In lane 11 the standard was diluted to 10%. (B) The quantification of standard by purified SNAP proteins. The standard was diluted to 20% and mixed with SNAP dye.

Article Snippet: S2 cells were lysed by 2 freeze-thaw cycles to avoid detergent in Native-PAGE samples using the following protocol: An S2 cell pellet from a 5 mL culture was resuspended with 400 μL buffer A (50 mM Tris, pH 8, NaCl 150 mM, 20% glycerol and 1x protease inhibitor; Cat# A32965, ThermoFisher).

Techniques: Multiplex Assay, Imaging, Fluorescence, Purification