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af4 device  (Waters Corporation)


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    Structured Review

    Waters Corporation af4 device
    <t>AF4</t> allows separation of the heterogeneous CVA9 virion population generated by 0.01% faf-BSA and endosomal ion treatments. (A) Two independent AF4 fractograms of untreated CVA9. (B) AF4 fractogram of CVA9 after 1-h treatment with 0.01% faf-BSA at 37°C. (C) AF4 fractogram of CVA9 after 3-h treatment with 0.01% faf-BSA at 37°C. (D) AF4 fractogram of CVA9 after 1-h treatment in endosomal ion environment at 37°C. (E) AF4 fractogram of CVA9 after 3-h treatment in endosomal ion environment at 37°C. (F) AF4 fractogram of CVA9 after combined treatment (0.01% faf-BSA in endosomal ionic environment) for 1 h at 37°C. In all panels, the x axis indicates time (1-mL fractions were collected at the rate of 0.5 mL/min); the y axis on the left shows light scattering (black or gray lines) and on the right the hydrodynamic radius is shown, as measured by online dynamic light scattering detector (black dots). The vertical dashed line on the left indicates the peak for intact particles and on the right the peak for expanded particles. AF4 fractions used for MS analysis are indicated by red boxes. The light scatter absorbance on all the fractograms was normalized to the highest light scatter absorbance peak, which is found in panel F.
    Af4 Device, supplied by Waters Corporation, 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
    af4 device - by Bioz Stars, 2026-10
    86/100 stars

    Images

    1) Product Images from "Structural Studies Reveal that Endosomal Cations Promote Formation of Infectious Coxsackievirus A9 A-Particles, Facilitating RNA and VP4 Release"

    Article Title: Structural Studies Reveal that Endosomal Cations Promote Formation of Infectious Coxsackievirus A9 A-Particles, Facilitating RNA and VP4 Release

    Journal: Journal of Virology

    doi: 10.1128/jvi.01367-22

    AF4 allows separation of the heterogeneous CVA9 virion population generated by 0.01% faf-BSA and endosomal ion treatments. (A) Two independent AF4 fractograms of untreated CVA9. (B) AF4 fractogram of CVA9 after 1-h treatment with 0.01% faf-BSA at 37°C. (C) AF4 fractogram of CVA9 after 3-h treatment with 0.01% faf-BSA at 37°C. (D) AF4 fractogram of CVA9 after 1-h treatment in endosomal ion environment at 37°C. (E) AF4 fractogram of CVA9 after 3-h treatment in endosomal ion environment at 37°C. (F) AF4 fractogram of CVA9 after combined treatment (0.01% faf-BSA in endosomal ionic environment) for 1 h at 37°C. In all panels, the x axis indicates time (1-mL fractions were collected at the rate of 0.5 mL/min); the y axis on the left shows light scattering (black or gray lines) and on the right the hydrodynamic radius is shown, as measured by online dynamic light scattering detector (black dots). The vertical dashed line on the left indicates the peak for intact particles and on the right the peak for expanded particles. AF4 fractions used for MS analysis are indicated by red boxes. The light scatter absorbance on all the fractograms was normalized to the highest light scatter absorbance peak, which is found in panel F.
    Figure Legend Snippet: AF4 allows separation of the heterogeneous CVA9 virion population generated by 0.01% faf-BSA and endosomal ion treatments. (A) Two independent AF4 fractograms of untreated CVA9. (B) AF4 fractogram of CVA9 after 1-h treatment with 0.01% faf-BSA at 37°C. (C) AF4 fractogram of CVA9 after 3-h treatment with 0.01% faf-BSA at 37°C. (D) AF4 fractogram of CVA9 after 1-h treatment in endosomal ion environment at 37°C. (E) AF4 fractogram of CVA9 after 3-h treatment in endosomal ion environment at 37°C. (F) AF4 fractogram of CVA9 after combined treatment (0.01% faf-BSA in endosomal ionic environment) for 1 h at 37°C. In all panels, the x axis indicates time (1-mL fractions were collected at the rate of 0.5 mL/min); the y axis on the left shows light scattering (black or gray lines) and on the right the hydrodynamic radius is shown, as measured by online dynamic light scattering detector (black dots). The vertical dashed line on the left indicates the peak for intact particles and on the right the peak for expanded particles. AF4 fractions used for MS analysis are indicated by red boxes. The light scatter absorbance on all the fractograms was normalized to the highest light scatter absorbance peak, which is found in panel F.

    Techniques Used: Generated

     AF4  results <xref ref-type= a " title=" AF4 results
    Figure Legend Snippet: AF4 results a

    Techniques Used:

    Related Articles

    Refractive Index:

    Article Title: Structural Studies Reveal that Endosomal Cations Promote Formation of Infectious Coxsackievirus A9 A-Particles, Facilitating RNA and VP4 Release
    Article Snippet: The AF4 experiments were performed using the Eclipse NEON FFF system (Wyatt Technology, Santa Barbara, USA) which included an Agilent 1260 Infinity II pump and autosampler, an analytical long channel with a dilution control module (Wyatt Technology), and an Agilent 1260 fraction collector. .. The AF4 device was coupled to an Optilab refractive index detector (Wyatt Technology), DAWN multiangle light scattering detector (MALS) with 18 angles (Wyatt Technology), online dynamic light scattering detector embedded in one of the DAWN angles (Wyatt Technology), and a UV detector (Agilent) set at 280 nm. .. Regenerated cellulose membrane at 10-kDa cutoff (Wyatt Technology lot number RIJB19432) and a Technology 525-μm spacer (Wyatt Technology lot number 247096) was used as the accumulation wall.

    Multi-Angle Light Scattering:

    Article Title: Structural Studies Reveal that Endosomal Cations Promote Formation of Infectious Coxsackievirus A9 A-Particles, Facilitating RNA and VP4 Release
    Article Snippet: The AF4 experiments were performed using the Eclipse NEON FFF system (Wyatt Technology, Santa Barbara, USA) which included an Agilent 1260 Infinity II pump and autosampler, an analytical long channel with a dilution control module (Wyatt Technology), and an Agilent 1260 fraction collector. .. The AF4 device was coupled to an Optilab refractive index detector (Wyatt Technology), DAWN multiangle light scattering detector (MALS) with 18 angles (Wyatt Technology), online dynamic light scattering detector embedded in one of the DAWN angles (Wyatt Technology), and a UV detector (Agilent) set at 280 nm. .. Regenerated cellulose membrane at 10-kDa cutoff (Wyatt Technology lot number RIJB19432) and a Technology 525-μm spacer (Wyatt Technology lot number 247096) was used as the accumulation wall.



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    <t>AF4</t> allows separation of the heterogeneous CVA9 virion population generated by 0.01% faf-BSA and endosomal ion treatments. (A) Two independent AF4 fractograms of untreated CVA9. (B) AF4 fractogram of CVA9 after 1-h treatment with 0.01% faf-BSA at 37°C. (C) AF4 fractogram of CVA9 after 3-h treatment with 0.01% faf-BSA at 37°C. (D) AF4 fractogram of CVA9 after 1-h treatment in endosomal ion environment at 37°C. (E) AF4 fractogram of CVA9 after 3-h treatment in endosomal ion environment at 37°C. (F) AF4 fractogram of CVA9 after combined treatment (0.01% faf-BSA in endosomal ionic environment) for 1 h at 37°C. In all panels, the x axis indicates time (1-mL fractions were collected at the rate of 0.5 mL/min); the y axis on the left shows light scattering (black or gray lines) and on the right the hydrodynamic radius is shown, as measured by online dynamic light scattering detector (black dots). The vertical dashed line on the left indicates the peak for intact particles and on the right the peak for expanded particles. AF4 fractions used for MS analysis are indicated by red boxes. The light scatter absorbance on all the fractograms was normalized to the highest light scatter absorbance peak, which is found in panel F.
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    Figure 1. Scheme of the two analytical focuses of this study. (a) Empty and filled AAV8 VLP particles are analyzed via nES GEMMA and AFM. (b) <t>AF4</t> liquid-phase <t>separation</t> enables AAV8 VLP oligomer analysis by means of nES GEMMA and AFM after fractionation.
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    Image Search Results


    AF4 allows separation of the heterogeneous CVA9 virion population generated by 0.01% faf-BSA and endosomal ion treatments. (A) Two independent AF4 fractograms of untreated CVA9. (B) AF4 fractogram of CVA9 after 1-h treatment with 0.01% faf-BSA at 37°C. (C) AF4 fractogram of CVA9 after 3-h treatment with 0.01% faf-BSA at 37°C. (D) AF4 fractogram of CVA9 after 1-h treatment in endosomal ion environment at 37°C. (E) AF4 fractogram of CVA9 after 3-h treatment in endosomal ion environment at 37°C. (F) AF4 fractogram of CVA9 after combined treatment (0.01% faf-BSA in endosomal ionic environment) for 1 h at 37°C. In all panels, the x axis indicates time (1-mL fractions were collected at the rate of 0.5 mL/min); the y axis on the left shows light scattering (black or gray lines) and on the right the hydrodynamic radius is shown, as measured by online dynamic light scattering detector (black dots). The vertical dashed line on the left indicates the peak for intact particles and on the right the peak for expanded particles. AF4 fractions used for MS analysis are indicated by red boxes. The light scatter absorbance on all the fractograms was normalized to the highest light scatter absorbance peak, which is found in panel F.

    Journal: Journal of Virology

    Article Title: Structural Studies Reveal that Endosomal Cations Promote Formation of Infectious Coxsackievirus A9 A-Particles, Facilitating RNA and VP4 Release

    doi: 10.1128/jvi.01367-22

    Figure Lengend Snippet: AF4 allows separation of the heterogeneous CVA9 virion population generated by 0.01% faf-BSA and endosomal ion treatments. (A) Two independent AF4 fractograms of untreated CVA9. (B) AF4 fractogram of CVA9 after 1-h treatment with 0.01% faf-BSA at 37°C. (C) AF4 fractogram of CVA9 after 3-h treatment with 0.01% faf-BSA at 37°C. (D) AF4 fractogram of CVA9 after 1-h treatment in endosomal ion environment at 37°C. (E) AF4 fractogram of CVA9 after 3-h treatment in endosomal ion environment at 37°C. (F) AF4 fractogram of CVA9 after combined treatment (0.01% faf-BSA in endosomal ionic environment) for 1 h at 37°C. In all panels, the x axis indicates time (1-mL fractions were collected at the rate of 0.5 mL/min); the y axis on the left shows light scattering (black or gray lines) and on the right the hydrodynamic radius is shown, as measured by online dynamic light scattering detector (black dots). The vertical dashed line on the left indicates the peak for intact particles and on the right the peak for expanded particles. AF4 fractions used for MS analysis are indicated by red boxes. The light scatter absorbance on all the fractograms was normalized to the highest light scatter absorbance peak, which is found in panel F.

    Article Snippet: The AF4 device was coupled to an Optilab refractive index detector (Wyatt Technology), DAWN multiangle light scattering detector (MALS) with 18 angles (Wyatt Technology), online dynamic light scattering detector embedded in one of the DAWN angles (Wyatt Technology), and a UV detector (Agilent) set at 280 nm.

    Techniques: Generated

     AF4  results <xref ref-type= a " width="100%" height="100%">

    Journal: Journal of Virology

    Article Title: Structural Studies Reveal that Endosomal Cations Promote Formation of Infectious Coxsackievirus A9 A-Particles, Facilitating RNA and VP4 Release

    doi: 10.1128/jvi.01367-22

    Figure Lengend Snippet: AF4 results a

    Article Snippet: The AF4 device was coupled to an Optilab refractive index detector (Wyatt Technology), DAWN multiangle light scattering detector (MALS) with 18 angles (Wyatt Technology), online dynamic light scattering detector embedded in one of the DAWN angles (Wyatt Technology), and a UV detector (Agilent) set at 280 nm.

    Techniques:

    Summary of the hyphenated  AF4  experimental design. Experiments were conducted in single runs or duplicates

    Journal: Analytical and Bioanalytical Chemistry

    Article Title: Optimization of hyphenated asymmetric flow field-flow fractionation for the analysis of silver nanoparticles in aqueous solutions

    doi: 10.1007/s00216-021-03647-3

    Figure Lengend Snippet: Summary of the hyphenated AF4 experimental design. Experiments were conducted in single runs or duplicates

    Article Snippet: The separation protocol comprised six consecutive steps, each characterized by its individual duration and applied cross-flow rate ( V x ) as shown in the example of Table S . For the evaluation of the quality of the separation and the characterization of the AgNP fractions’ optical properties, UV/Vis spectra were recorded using a Shimadzu SPD-M10Avp photodiode array detector (PDA, graphical abstract) linked to the Eclipse AF4 device with 0.25-mm ID PEEK tubing and controlled with a SCL-10Avp unit via the LCsolution software 1.03 SP3 (Shimadzu).

    Techniques:

    Size characterization of AgNP_LA in batch and in  AF4-UV/Vis-DLS  system. Results obtained with the ZetaSizer Nano-ZS for the hydrodynamic diameter d H , polydispersity index PdI , and zeta-potential ζ . Parenthesized values were determined ca. 4 months after purchasing the AgNPs; all other values were determined directly after delivery. AF4 experiments were conducted within 2 months after AgNP delivery. Values shown in the table for 1:1 AgNP_LA mixtures were acquired with the best experimental conditions

    Journal: Analytical and Bioanalytical Chemistry

    Article Title: Optimization of hyphenated asymmetric flow field-flow fractionation for the analysis of silver nanoparticles in aqueous solutions

    doi: 10.1007/s00216-021-03647-3

    Figure Lengend Snippet: Size characterization of AgNP_LA in batch and in AF4-UV/Vis-DLS system. Results obtained with the ZetaSizer Nano-ZS for the hydrodynamic diameter d H , polydispersity index PdI , and zeta-potential ζ . Parenthesized values were determined ca. 4 months after purchasing the AgNPs; all other values were determined directly after delivery. AF4 experiments were conducted within 2 months after AgNP delivery. Values shown in the table for 1:1 AgNP_LA mixtures were acquired with the best experimental conditions

    Article Snippet: The separation protocol comprised six consecutive steps, each characterized by its individual duration and applied cross-flow rate ( V x ) as shown in the example of Table S . For the evaluation of the quality of the separation and the characterization of the AgNP fractions’ optical properties, UV/Vis spectra were recorded using a Shimadzu SPD-M10Avp photodiode array detector (PDA, graphical abstract) linked to the Eclipse AF4 device with 0.25-mm ID PEEK tubing and controlled with a SCL-10Avp unit via the LCsolution software 1.03 SP3 (Shimadzu).

    Techniques:

    Fractograms and hydrodynamic diameter of a 1:1 mixture of 20-nm and 80-nm AgNP_LA acquired with V x = 0.5 mL/min and 0.05% v/v Mucasol as carrier solution. Black color refers to a mixture prepared in ultrapure water; red color refers to the preparation in fjord water and injection into the AF4 system 20 min after preparation

    Journal: Analytical and Bioanalytical Chemistry

    Article Title: Optimization of hyphenated asymmetric flow field-flow fractionation for the analysis of silver nanoparticles in aqueous solutions

    doi: 10.1007/s00216-021-03647-3

    Figure Lengend Snippet: Fractograms and hydrodynamic diameter of a 1:1 mixture of 20-nm and 80-nm AgNP_LA acquired with V x = 0.5 mL/min and 0.05% v/v Mucasol as carrier solution. Black color refers to a mixture prepared in ultrapure water; red color refers to the preparation in fjord water and injection into the AF4 system 20 min after preparation

    Article Snippet: The separation protocol comprised six consecutive steps, each characterized by its individual duration and applied cross-flow rate ( V x ) as shown in the example of Table S . For the evaluation of the quality of the separation and the characterization of the AgNP fractions’ optical properties, UV/Vis spectra were recorded using a Shimadzu SPD-M10Avp photodiode array detector (PDA, graphical abstract) linked to the Eclipse AF4 device with 0.25-mm ID PEEK tubing and controlled with a SCL-10Avp unit via the LCsolution software 1.03 SP3 (Shimadzu).

    Techniques: Injection

    Figure 1. Scheme of the two analytical focuses of this study. (a) Empty and filled AAV8 VLP particles are analyzed via nES GEMMA and AFM. (b) AF4 liquid-phase separation enables AAV8 VLP oligomer analysis by means of nES GEMMA and AFM after fractionation.

    Journal: ACS omega

    Article Title: Adeno-associated Virus Virus-like Particle Characterization via Orthogonal Methods: Nanoelectrospray Differential Mobility Analysis, Asymmetric Flow Field-Flow Fractionation, and Atomic Force Microscopy.

    doi: 10.1021/acsomega.1c01443

    Figure Lengend Snippet: Figure 1. Scheme of the two analytical focuses of this study. (a) Empty and filled AAV8 VLP particles are analyzed via nES GEMMA and AFM. (b) AF4 liquid-phase separation enables AAV8 VLP oligomer analysis by means of nES GEMMA and AFM after fractionation.

    Article Snippet: The capillary is manually cut and tapered with a homebuilt grinding machine based on the work of Tycova et al.15 AF4 experiments were performed on an Agilent 1200 system (Agilent Technologies, Santa Clara, CA, USA, auto sampler, pump, and detector), which consisted of an auto sampler, HPLC pumps, an AF4 separation device (Wyatt Technology, Santa Barbara, CA, USA), and a fluorescence detector (λex/em = 280/340 nm).

    Techniques: Gas Phase Electrophoretic Molecular Mobility Analysis, Fractionation

    Figure 2. Implications of the buffer exchange treatment. (a) nES GEMMA spectra of the sample before (black trace) and after (red trace) desalting. Nonvolatile salts and other components (3−15 nm) are drastically reduced. The inset shows the shift toward small EM diameter of the AAV8 VLP’s peak. (b) AF4 fractogram of the sample with (red trace) or without (blue trace) a buffer exchange procedure. Both nES GEMMA spectra (a) and (b) show reduced signal intensity for the AAV8 VLP’s peak due to sample loss during the desalting treatment.

    Journal: ACS omega

    Article Title: Adeno-associated Virus Virus-like Particle Characterization via Orthogonal Methods: Nanoelectrospray Differential Mobility Analysis, Asymmetric Flow Field-Flow Fractionation, and Atomic Force Microscopy.

    doi: 10.1021/acsomega.1c01443

    Figure Lengend Snippet: Figure 2. Implications of the buffer exchange treatment. (a) nES GEMMA spectra of the sample before (black trace) and after (red trace) desalting. Nonvolatile salts and other components (3−15 nm) are drastically reduced. The inset shows the shift toward small EM diameter of the AAV8 VLP’s peak. (b) AF4 fractogram of the sample with (red trace) or without (blue trace) a buffer exchange procedure. Both nES GEMMA spectra (a) and (b) show reduced signal intensity for the AAV8 VLP’s peak due to sample loss during the desalting treatment.

    Article Snippet: The capillary is manually cut and tapered with a homebuilt grinding machine based on the work of Tycova et al.15 AF4 experiments were performed on an Agilent 1200 system (Agilent Technologies, Santa Clara, CA, USA, auto sampler, pump, and detector), which consisted of an auto sampler, HPLC pumps, an AF4 separation device (Wyatt Technology, Santa Barbara, CA, USA), and a fluorescence detector (λex/em = 280/340 nm).

    Techniques: Gas Phase Electrophoretic Molecular Mobility Analysis

    Figure 4. Stressing procedure and fractionation of the sample. (a) AF4 fractogram of control (blue trace) and heat/mechanical-stressed (magenta trace) sample. (b) The red vertical lines mark the collected fractions: 16.5−19.2 min monomer fraction; 19.2−20.6 min dimer and trimer fraction; 20.6−25.0 min higher oligomeric fraction.

    Journal: ACS omega

    Article Title: Adeno-associated Virus Virus-like Particle Characterization via Orthogonal Methods: Nanoelectrospray Differential Mobility Analysis, Asymmetric Flow Field-Flow Fractionation, and Atomic Force Microscopy.

    doi: 10.1021/acsomega.1c01443

    Figure Lengend Snippet: Figure 4. Stressing procedure and fractionation of the sample. (a) AF4 fractogram of control (blue trace) and heat/mechanical-stressed (magenta trace) sample. (b) The red vertical lines mark the collected fractions: 16.5−19.2 min monomer fraction; 19.2−20.6 min dimer and trimer fraction; 20.6−25.0 min higher oligomeric fraction.

    Article Snippet: The capillary is manually cut and tapered with a homebuilt grinding machine based on the work of Tycova et al.15 AF4 experiments were performed on an Agilent 1200 system (Agilent Technologies, Santa Clara, CA, USA, auto sampler, pump, and detector), which consisted of an auto sampler, HPLC pumps, an AF4 separation device (Wyatt Technology, Santa Barbara, CA, USA), and a fluorescence detector (λex/em = 280/340 nm).

    Techniques: Fractionation, Control

    Figure 5. nES GEMMA spectra and AFM images of the three fractions collected with the AF4 technique (see Figure 4b). (a, b) Monomer (M) fraction; (c, d) dimer (D) and trimer (T) fraction; and (e, f) higher oligomeric (O) fraction. nES GEMMA spectra compare signals obtained for VLP-containing samples (red traces) and blanks recorded for a NH4OAc blank (black traces), respectively. nES GEMMA signals below 20 nm EM diameter putatively correspond to incompletely removed, aggregating AF4 buffer components. In (f), the arrow indicates an AAV8 VLP higher oligomer with a height of 35 nm.

    Journal: ACS omega

    Article Title: Adeno-associated Virus Virus-like Particle Characterization via Orthogonal Methods: Nanoelectrospray Differential Mobility Analysis, Asymmetric Flow Field-Flow Fractionation, and Atomic Force Microscopy.

    doi: 10.1021/acsomega.1c01443

    Figure Lengend Snippet: Figure 5. nES GEMMA spectra and AFM images of the three fractions collected with the AF4 technique (see Figure 4b). (a, b) Monomer (M) fraction; (c, d) dimer (D) and trimer (T) fraction; and (e, f) higher oligomeric (O) fraction. nES GEMMA spectra compare signals obtained for VLP-containing samples (red traces) and blanks recorded for a NH4OAc blank (black traces), respectively. nES GEMMA signals below 20 nm EM diameter putatively correspond to incompletely removed, aggregating AF4 buffer components. In (f), the arrow indicates an AAV8 VLP higher oligomer with a height of 35 nm.

    Article Snippet: The capillary is manually cut and tapered with a homebuilt grinding machine based on the work of Tycova et al.15 AF4 experiments were performed on an Agilent 1200 system (Agilent Technologies, Santa Clara, CA, USA, auto sampler, pump, and detector), which consisted of an auto sampler, HPLC pumps, an AF4 separation device (Wyatt Technology, Santa Barbara, CA, USA), and a fluorescence detector (λex/em = 280/340 nm).

    Techniques: Gas Phase Electrophoretic Molecular Mobility Analysis