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su 8 spacer  (Silson Ltd)

 
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    Structured Review

    Silson Ltd su 8 spacer
    Experimental setup. ( a ) Schematic side view of the dedicated flow chamber (see legend for the individual components). Two SiN membranes are separated by 20 µm <t>using</t> <t>SU-8</t> spacers. This ‘sandwich’ is enclosed by PDMS layers and clamped by metal frames. The buffer flow is represented by blue dashed arrows. ( b ) Schematic drawing of the SAXS experiment (not to scale). The sample (fixed-hydrated cells on a SiN membrane) is scanned through the focused X-rays. The beamstop blocks the direct beam, and the two-dimensional detector records the scattered X-rays. The red dashed lines represent the scattering angle 2θ between the incoming beam direction and the scattered X-rays. ( c ) The flow within the microfluidic chamber is oriented horizontally in perpendicular direction to the incoming beam, thus along the y axis. ( d ) Representation of the scanning scheme; the SiN membrane is moved along the y and z axes to obtain a raster scan of the selected region with the specified step numbers and sizes.
    Su 8 Spacer, supplied by Silson Ltd, 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/result/su 8 spacer/product/Silson Ltd
    Average 86 stars, based on 1 article reviews
    su 8 spacer - by Bioz Stars, 2026-05
    86/100 stars

    Images

    1) Product Images from "Fast-scanning small-angle X-ray scattering of hydrated biological cells"

    Article Title: Fast-scanning small-angle X-ray scattering of hydrated biological cells

    Journal: Journal of Synchrotron Radiation

    doi: 10.1107/S1600577526002018

    Experimental setup. ( a ) Schematic side view of the dedicated flow chamber (see legend for the individual components). Two SiN membranes are separated by 20 µm using SU-8 spacers. This ‘sandwich’ is enclosed by PDMS layers and clamped by metal frames. The buffer flow is represented by blue dashed arrows. ( b ) Schematic drawing of the SAXS experiment (not to scale). The sample (fixed-hydrated cells on a SiN membrane) is scanned through the focused X-rays. The beamstop blocks the direct beam, and the two-dimensional detector records the scattered X-rays. The red dashed lines represent the scattering angle 2θ between the incoming beam direction and the scattered X-rays. ( c ) The flow within the microfluidic chamber is oriented horizontally in perpendicular direction to the incoming beam, thus along the y axis. ( d ) Representation of the scanning scheme; the SiN membrane is moved along the y and z axes to obtain a raster scan of the selected region with the specified step numbers and sizes.
    Figure Legend Snippet: Experimental setup. ( a ) Schematic side view of the dedicated flow chamber (see legend for the individual components). Two SiN membranes are separated by 20 µm using SU-8 spacers. This ‘sandwich’ is enclosed by PDMS layers and clamped by metal frames. The buffer flow is represented by blue dashed arrows. ( b ) Schematic drawing of the SAXS experiment (not to scale). The sample (fixed-hydrated cells on a SiN membrane) is scanned through the focused X-rays. The beamstop blocks the direct beam, and the two-dimensional detector records the scattered X-rays. The red dashed lines represent the scattering angle 2θ between the incoming beam direction and the scattered X-rays. ( c ) The flow within the microfluidic chamber is oriented horizontally in perpendicular direction to the incoming beam, thus along the y axis. ( d ) Representation of the scanning scheme; the SiN membrane is moved along the y and z axes to obtain a raster scan of the selected region with the specified step numbers and sizes.

    Techniques Used: Membrane



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    su 8 spacer  (Silson Ltd)
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    Experimental setup. ( a ) Schematic side view of the dedicated flow chamber (see legend for the individual components). Two SiN membranes are separated by 20 µm <t>using</t> <t>SU-8</t> spacers. This ‘sandwich’ is enclosed by PDMS layers and clamped by metal frames. The buffer flow is represented by blue dashed arrows. ( b ) Schematic drawing of the SAXS experiment (not to scale). The sample (fixed-hydrated cells on a SiN membrane) is scanned through the focused X-rays. The beamstop blocks the direct beam, and the two-dimensional detector records the scattered X-rays. The red dashed lines represent the scattering angle 2θ between the incoming beam direction and the scattered X-rays. ( c ) The flow within the microfluidic chamber is oriented horizontally in perpendicular direction to the incoming beam, thus along the y axis. ( d ) Representation of the scanning scheme; the SiN membrane is moved along the y and z axes to obtain a raster scan of the selected region with the specified step numbers and sizes.
    Su 8 Spacer, supplied by Silson Ltd, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 86 stars, based on 1 article reviews
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    sin chips thick su-8 spacers  (Hummingbird Scientific)
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    Experimental setup. ( a ) Schematic side view of the dedicated flow chamber (see legend for the individual components). Two SiN membranes are separated by 20 µm <t>using</t> <t>SU-8</t> spacers. This ‘sandwich’ is enclosed by PDMS layers and clamped by metal frames. The buffer flow is represented by blue dashed arrows. ( b ) Schematic drawing of the SAXS experiment (not to scale). The sample (fixed-hydrated cells on a SiN membrane) is scanned through the focused X-rays. The beamstop blocks the direct beam, and the two-dimensional detector records the scattered X-rays. The red dashed lines represent the scattering angle 2θ between the incoming beam direction and the scattered X-rays. ( c ) The flow within the microfluidic chamber is oriented horizontally in perpendicular direction to the incoming beam, thus along the y axis. ( d ) Representation of the scanning scheme; the SiN membrane is moved along the y and z axes to obtain a raster scan of the selected region with the specified step numbers and sizes.
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    Experimental setup. ( a ) Schematic side view of the dedicated flow chamber (see legend for the individual components). Two SiN membranes are separated by 20 µm <t>using</t> <t>SU-8</t> spacers. This ‘sandwich’ is enclosed by PDMS layers and clamped by metal frames. The buffer flow is represented by blue dashed arrows. ( b ) Schematic drawing of the SAXS experiment (not to scale). The sample (fixed-hydrated cells on a SiN membrane) is scanned through the focused X-rays. The beamstop blocks the direct beam, and the two-dimensional detector records the scattered X-rays. The red dashed lines represent the scattering angle 2θ between the incoming beam direction and the scattered X-rays. ( c ) The flow within the microfluidic chamber is oriented horizontally in perpendicular direction to the incoming beam, thus along the y axis. ( d ) Representation of the scanning scheme; the SiN membrane is moved along the y and z axes to obtain a raster scan of the selected region with the specified step numbers and sizes.
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    Image Search Results


    Experimental setup. ( a ) Schematic side view of the dedicated flow chamber (see legend for the individual components). Two SiN membranes are separated by 20 µm using SU-8 spacers. This ‘sandwich’ is enclosed by PDMS layers and clamped by metal frames. The buffer flow is represented by blue dashed arrows. ( b ) Schematic drawing of the SAXS experiment (not to scale). The sample (fixed-hydrated cells on a SiN membrane) is scanned through the focused X-rays. The beamstop blocks the direct beam, and the two-dimensional detector records the scattered X-rays. The red dashed lines represent the scattering angle 2θ between the incoming beam direction and the scattered X-rays. ( c ) The flow within the microfluidic chamber is oriented horizontally in perpendicular direction to the incoming beam, thus along the y axis. ( d ) Representation of the scanning scheme; the SiN membrane is moved along the y and z axes to obtain a raster scan of the selected region with the specified step numbers and sizes.

    Journal: Journal of Synchrotron Radiation

    Article Title: Fast-scanning small-angle X-ray scattering of hydrated biological cells

    doi: 10.1107/S1600577526002018

    Figure Lengend Snippet: Experimental setup. ( a ) Schematic side view of the dedicated flow chamber (see legend for the individual components). Two SiN membranes are separated by 20 µm using SU-8 spacers. This ‘sandwich’ is enclosed by PDMS layers and clamped by metal frames. The buffer flow is represented by blue dashed arrows. ( b ) Schematic drawing of the SAXS experiment (not to scale). The sample (fixed-hydrated cells on a SiN membrane) is scanned through the focused X-rays. The beamstop blocks the direct beam, and the two-dimensional detector records the scattered X-rays. The red dashed lines represent the scattering angle 2θ between the incoming beam direction and the scattered X-rays. ( c ) The flow within the microfluidic chamber is oriented horizontally in perpendicular direction to the incoming beam, thus along the y axis. ( d ) Representation of the scanning scheme; the SiN membrane is moved along the y and z axes to obtain a raster scan of the selected region with the specified step numbers and sizes.

    Article Snippet: When fully assembled, the sample chamber is composed of two SiN membranes, one of which the cells are grown, and the other one with an SU-8 spacer of a thickness of 20 μm (Silson Ltd) on its flat side [see Fig. 1 ( a ) and Fig. S1( c ) for more details], thereby enabling liquid flow over the window region.

    Techniques: Membrane