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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/pm40407396-20-7-35?v=VitroCom+Inc
    Average 90 stars, based on 1 article reviews
    square cross-section glass capillary tubing - by Bioz Stars, 2026-07
    90/100 stars

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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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    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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    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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    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