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square cross-section glass capillary tubing  (VitroCom Inc)

 
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    VitroCom Inc square cross-section glass capillary tubing
    Square Cross Section Glass Capillary Tubing, supplied by VitroCom Inc, 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/square+glass+capillary/glass+capillaries/pm40407396-20-7-35
    Average 90 stars, based on 1 article reviews
    square cross-section glass capillary tubing - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    Crystallization Assay:

    Article Title: Direct observation and control of non-classical crystallization pathways in binary colloidal systems.
    Article Snippet: .. Crystallization under continuous dialysis To perform experiments at variable interaction potentials, mixtures of oppositely charged PS particles with 4.5 mM NaCl and 0.1 wt% F108 were introduced into 50-mm-long glass capillaries (inner dimensions: 2.0 mm × 0.2 mm, VitroCom) and sealed at one end. ..

    other:

    Article Title: A flow-through mechanical trap for repetitive analysis of individual particles.
    Article Snippet: We describe the construction of a flow-through analyzer with a mechanical fluidic control system that allows individual particles such as beads or cells to be trapped repeatedly for optical analysis.. This instrument allows long measurements of particles sampled from rapid flow and can be used to determine contributions to measurement variance and individuate environmental perturbations on single cells.. The demonstration system described here includes basic detection channels for forward-scattered light and fluorescence, a pinch-valve based trap, a mechanism for controlling the position of trapped particles, and a holding loop for long-duration studies of single particles.



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    Time course of ThT fibril growth assay and capillary flocculation assay from ESI Video 1 and 2. (A) ThT fluorescence of amyloid fibril growth with and without PK. The dashed line indicates addition of monomer to all samples. PK treatment is notated by color-coded arrows. PK is both added and inhibited before the addition of fresh monomer outside the plate-reader instrument. However, the treatment time, where no data is gathered, is not shown in this graph. ThT is added to samples labeled “w/o ThT” along with additional monomer. Numbering indicates technical repeats. (B) Sample images of <t>capillaries</t> from ESI Video 1 and 2 at time 0 and 180 min. (C) Normalized intensity of ThT-fluorescence throughout the experiment. (D) Change in relative spatial standard deviation of ThT-fluorescence intensity across the capillary as a function of time.
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    Image Search Results


    Time course of ThT fibril growth assay and capillary flocculation assay from ESI Video 1 and 2. (A) ThT fluorescence of amyloid fibril growth with and without PK. The dashed line indicates addition of monomer to all samples. PK treatment is notated by color-coded arrows. PK is both added and inhibited before the addition of fresh monomer outside the plate-reader instrument. However, the treatment time, where no data is gathered, is not shown in this graph. ThT is added to samples labeled “w/o ThT” along with additional monomer. Numbering indicates technical repeats. (B) Sample images of capillaries from ESI Video 1 and 2 at time 0 and 180 min. (C) Normalized intensity of ThT-fluorescence throughout the experiment. (D) Change in relative spatial standard deviation of ThT-fluorescence intensity across the capillary as a function of time.

    Journal: RSC Advances

    Article Title: Probing the effect of the disordered flank regions on amyloid fibril growth and proliferation †

    doi: 10.1039/d5ra01654a

    Figure Lengend Snippet: Time course of ThT fibril growth assay and capillary flocculation assay from ESI Video 1 and 2. (A) ThT fluorescence of amyloid fibril growth with and without PK. The dashed line indicates addition of monomer to all samples. PK treatment is notated by color-coded arrows. PK is both added and inhibited before the addition of fresh monomer outside the plate-reader instrument. However, the treatment time, where no data is gathered, is not shown in this graph. ThT is added to samples labeled “w/o ThT” along with additional monomer. Numbering indicates technical repeats. (B) Sample images of capillaries from ESI Video 1 and 2 at time 0 and 180 min. (C) Normalized intensity of ThT-fluorescence throughout the experiment. (D) Change in relative spatial standard deviation of ThT-fluorescence intensity across the capillary as a function of time.

    Article Snippet: Capillary flocculation assays were performed using square glass capillaries of 0.4 mm inner diameter and walls of 0.2 mm (VitroCom, Mountain Lakes, NJ, USA).

    Techniques: Growth Assay, Flocculation, Fluorescence, Labeling, W/O, Standard Deviation