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flow module  (Biolin Scientific)


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    Structured Review

    Biolin Scientific flow module
    Flow Module, supplied by Biolin Scientific, used in various techniques. Bioz Stars score: 94/100, based on 43 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/flow+module/QFM+401+Flow+module/pm41922476-249-13-25
    Average 94 stars, based on 43 article reviews
    flow module - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    QCM-D:

    Article Title: Electrochemical biosensing of cerium with a tyrosine‐functionalized <scp>EF</scp>‐hand loop peptide
    Article Snippet: .. A QCM-D instrument (QSense Explorer, Biolin Scientific), integrated Q-Soft software (Biolin Scientific), a flow module (QFM 401), a peristaltic pump (LABINETT, RS232IN), and gold-coated crystal sensors (QSX 301, 5 MHz, Biolin Scientific) were used to record shifts in frequency (Δf ) and dissipation (ΔD) with time as peptides and ions adsorb to a gold surface. ..

    Article Title: Monitoring and Characterization of Milk Fouling on Stainless Steel Using a High-Pressure High-Temperature Quartz Crystal Microbalance with Dissipation.
    Article Snippet: Fouling at interfaces deteriorates the efficiency and hygiene of processes within numerous industrial sectors, including the oil and gas, biomedical device, and food industries.. In the food industry, the fouling of a complex food matrix to a heated stainless steel surface reduces production efficiency by increasing heating resistance, pumping requirements, and the frequency of cleaning operations.. In this work, quartz crystal microbalance with dissipation (QCM-D) was used to study the interface formed by the fouling of milk on a stainless steel surface at different flow rates and protein concentrations at high temperatures (135 °C).

    Article Title: Using cyclic voltammetry to probe the conformational transition of short elastin-like peptides.
    Article Snippet: .. The QCM-D instrument (QSense Explorer, Biolin Scientific) specifications and cleaning processes for the flow module (QFM 401) and gold-coated crystal sensors (QSX 301, 5 MHz, Biolin Scientific) have been thoroughly explained in our previous work39. ..

    Software:

    Article Title: Electrochemical biosensing of cerium with a tyrosine‐functionalized <scp>EF</scp>‐hand loop peptide
    Article Snippet: .. A QCM-D instrument (QSense Explorer, Biolin Scientific), integrated Q-Soft software (Biolin Scientific), a flow module (QFM 401), a peristaltic pump (LABINETT, RS232IN), and gold-coated crystal sensors (QSX 301, 5 MHz, Biolin Scientific) were used to record shifts in frequency (Δf ) and dissipation (ΔD) with time as peptides and ions adsorb to a gold surface. ..

    Control:

    Article Title: Low-fouling properties in serum of carboxylic-oligo(ethylene glycol)-based interfaces
    Article Snippet: QCM-D assessment suggests the existence of two different protein adsorption regimes (a faster and a slower one) in OEG SAM structures.. Also, OEG SAM low-fouling features were confirmed by a lower protein loading when compared with bare gold.. A R T I C L E I N F O

    other:

    Article Title: Environmentally stable and stretchable polymer electronics enabled by surface-tethered nanostructured molecular-level protection.
    Article Snippet: Stretchable polymer semiconductors (PSCs) are essential for soft stretchable electronics.. However, their environmental stability remains a longstanding concern.. Here we report a surface-tethered stretchable molecular protecting layer to realize stretchable polymer electronics that are stable in direct contact with physiological fluids, containing water, ions and biofluids.



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    Biolin Scientific qfm 401 flow module cell
    (A) From superior to inferior and left to right: (1) Right External Jugular Vein – 7 Fr. cannula for central venous pressure (CVP) monitoring, (2) Left External Jugular vein – 7 Fr. triple lumen catheter for for fluid and drug administration, (3) Left Carotid Artery, 3-4mm <t>Perivascular</t> Transonic flow probe, (4) Left Subclavian Artery – 7Fr Cannula for proximal arterial pressure monitoring, (5) Right Brachial Artery, 5Fr. catheter for blood sampling, (6) Brachiocephalic arterial trunk, 6-8mm Perivascular Transonic flow probe, (7) Ascending Aorta (aortic root), 20-24mm Perivascular Transonic flow probe, (8) Left Ventricle, Transonic Pressure-Volume Catheter introduced via apical stick, (9) Proximal Descending Aorta, 12-14mm Perivascular Transonic Flow probe, (10) Left Renal Artery, 3-4 mm Perivascular Transonic Flow probe, (11) Distal Descending Aorta, 6-8 mm Perivascular Transonic flow probe, (12) Right Femoral Artery – 7 Fr. cannula reserved for distal pressure monitoring generally positioned infrarenal, (13) Left Femoral Artery - 9 Fr. cannula for introduction of the balloon catheter (balloon is inflated in the figure), (14) Left Femoral Vein – 9 Fr. MAC catheter for hemorrhage, transfusion and fluid resuscitation via automated Masterflex pump, and (15) Foley catheter for urine collection. Not depicted in the illustration are the endotracheal tube, splenectomy, or rectal temperature probe. We’d like to acknowledge Mr. Jerry Louis Shelton at Texas A&M University for his assistance in generating the pig illustration in panel 1A. (B) Experimental timeline depicting controlled 30-minute hemorrhage period, followed by 30 minutes of aortic occlusion, a 10-minute balloon wean and 3-hour critical care resuscitation phase. Animals were randomized to 10%, 20% or 30% hemorrhage (by volume), and then randomized to either no aortic occlusion, partial REBOA (p-REBOA) and full REBOA (f-REBOA) intervention groups. Autologous blood re-transfusion and balloon weaning occurred between 65–75 minutes, after which a closed-loop critical care algorithm was initiated to maintain target MAP>65 mmHg for three hours (until time 240 minutes).
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    Image Search Results


    (A) From superior to inferior and left to right: (1) Right External Jugular Vein – 7 Fr. cannula for central venous pressure (CVP) monitoring, (2) Left External Jugular vein – 7 Fr. triple lumen catheter for for fluid and drug administration, (3) Left Carotid Artery, 3-4mm Perivascular Transonic flow probe, (4) Left Subclavian Artery – 7Fr Cannula for proximal arterial pressure monitoring, (5) Right Brachial Artery, 5Fr. catheter for blood sampling, (6) Brachiocephalic arterial trunk, 6-8mm Perivascular Transonic flow probe, (7) Ascending Aorta (aortic root), 20-24mm Perivascular Transonic flow probe, (8) Left Ventricle, Transonic Pressure-Volume Catheter introduced via apical stick, (9) Proximal Descending Aorta, 12-14mm Perivascular Transonic Flow probe, (10) Left Renal Artery, 3-4 mm Perivascular Transonic Flow probe, (11) Distal Descending Aorta, 6-8 mm Perivascular Transonic flow probe, (12) Right Femoral Artery – 7 Fr. cannula reserved for distal pressure monitoring generally positioned infrarenal, (13) Left Femoral Artery - 9 Fr. cannula for introduction of the balloon catheter (balloon is inflated in the figure), (14) Left Femoral Vein – 9 Fr. MAC catheter for hemorrhage, transfusion and fluid resuscitation via automated Masterflex pump, and (15) Foley catheter for urine collection. Not depicted in the illustration are the endotracheal tube, splenectomy, or rectal temperature probe. We’d like to acknowledge Mr. Jerry Louis Shelton at Texas A&M University for his assistance in generating the pig illustration in panel 1A. (B) Experimental timeline depicting controlled 30-minute hemorrhage period, followed by 30 minutes of aortic occlusion, a 10-minute balloon wean and 3-hour critical care resuscitation phase. Animals were randomized to 10%, 20% or 30% hemorrhage (by volume), and then randomized to either no aortic occlusion, partial REBOA (p-REBOA) and full REBOA (f-REBOA) intervention groups. Autologous blood re-transfusion and balloon weaning occurred between 65–75 minutes, after which a closed-loop critical care algorithm was initiated to maintain target MAP>65 mmHg for three hours (until time 240 minutes).

    Journal: bioRxiv

    Article Title: A translational porcine model to assess the graded impact of hemorrhage and aortic occlusion on cardiovascular hemodynamics and renal perfusion

    doi: 10.64898/2026.02.05.703869

    Figure Lengend Snippet: (A) From superior to inferior and left to right: (1) Right External Jugular Vein – 7 Fr. cannula for central venous pressure (CVP) monitoring, (2) Left External Jugular vein – 7 Fr. triple lumen catheter for for fluid and drug administration, (3) Left Carotid Artery, 3-4mm Perivascular Transonic flow probe, (4) Left Subclavian Artery – 7Fr Cannula for proximal arterial pressure monitoring, (5) Right Brachial Artery, 5Fr. catheter for blood sampling, (6) Brachiocephalic arterial trunk, 6-8mm Perivascular Transonic flow probe, (7) Ascending Aorta (aortic root), 20-24mm Perivascular Transonic flow probe, (8) Left Ventricle, Transonic Pressure-Volume Catheter introduced via apical stick, (9) Proximal Descending Aorta, 12-14mm Perivascular Transonic Flow probe, (10) Left Renal Artery, 3-4 mm Perivascular Transonic Flow probe, (11) Distal Descending Aorta, 6-8 mm Perivascular Transonic flow probe, (12) Right Femoral Artery – 7 Fr. cannula reserved for distal pressure monitoring generally positioned infrarenal, (13) Left Femoral Artery - 9 Fr. cannula for introduction of the balloon catheter (balloon is inflated in the figure), (14) Left Femoral Vein – 9 Fr. MAC catheter for hemorrhage, transfusion and fluid resuscitation via automated Masterflex pump, and (15) Foley catheter for urine collection. Not depicted in the illustration are the endotracheal tube, splenectomy, or rectal temperature probe. We’d like to acknowledge Mr. Jerry Louis Shelton at Texas A&M University for his assistance in generating the pig illustration in panel 1A. (B) Experimental timeline depicting controlled 30-minute hemorrhage period, followed by 30 minutes of aortic occlusion, a 10-minute balloon wean and 3-hour critical care resuscitation phase. Animals were randomized to 10%, 20% or 30% hemorrhage (by volume), and then randomized to either no aortic occlusion, partial REBOA (p-REBOA) and full REBOA (f-REBOA) intervention groups. Autologous blood re-transfusion and balloon weaning occurred between 65–75 minutes, after which a closed-loop critical care algorithm was initiated to maintain target MAP>65 mmHg for three hours (until time 240 minutes).

    Article Snippet: To monitor the hemodynamic response, we used a Perivascular Flow Module with six ultrasonic flow probes (TS420, Transonic Systems Inc., Ithaca, NY).

    Techniques: Sampling