quantification of the regional properties of gastric motility using dynamic magnetic resonance images Search Results


magnetm halotag ® magnetic affinity beads  (Promega)
90
Promega magnetm halotag ® magnetic affinity beads
(A) Heat map of relative abundance of 40 proteins shared between WDR76 and histones. The color intensity represents protein abundance with bright yellow displaying highest abundance (average distributed spectral counts) and black indicates that the protein was not detected in a particular purification. (B) Western blots of inputs and purifications from Halo-WDR76 stable cell line or HEK293FRT parental cell line shows that PARP1 and XRCC5 can be co-purified with WDR76, which is consistent with the proteomics analysis. Lane 1 and 2 are whole cell lysates from Halo-WDR76 stable cell line or HEK293FRT cells. Lane 3 and 4 are the protein purified with <t>HaloTag™</t> magnetic beads from Halo-WDR76 stable cell line or HEK293FRT cells. The top panel was blotted with anti-PARP1 and anti-Actin antibodies; the middle panel was blotted with anti-XRCC5 and anti-Actin antibodies; the last panel was blotted with anti-WDR76 and anti- HaloTag™, which was not detected because of the cleavage during elution. (C) Topological data analysis was performed on 164 proteins with a Z-score greater than 2 in WDR76 and at least one histone purification compared to controls. All the nodes in the network are colored based on metric PCA coordinate 2. Filters with variance normalized Euclidean metric were used (resolution 30, gain 3.0x).
Magnetm Halotag ® Magnetic Affinity Beads, supplied by Promega, 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/result/magnetm halotag ® magnetic affinity beads/product/Promega
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magnetm halotag ® magnetic affinity beads - by Bioz Stars, 2026-05
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magnetic labels (magneto-enzyme)  (Magna Biosciences)
90
Magna Biosciences magnetic labels (magneto-enzyme)
(A) Heat map of relative abundance of 40 proteins shared between WDR76 and histones. The color intensity represents protein abundance with bright yellow displaying highest abundance (average distributed spectral counts) and black indicates that the protein was not detected in a particular purification. (B) Western blots of inputs and purifications from Halo-WDR76 stable cell line or HEK293FRT parental cell line shows that PARP1 and XRCC5 can be co-purified with WDR76, which is consistent with the proteomics analysis. Lane 1 and 2 are whole cell lysates from Halo-WDR76 stable cell line or HEK293FRT cells. Lane 3 and 4 are the protein purified with <t>HaloTag™</t> magnetic beads from Halo-WDR76 stable cell line or HEK293FRT cells. The top panel was blotted with anti-PARP1 and anti-Actin antibodies; the middle panel was blotted with anti-XRCC5 and anti-Actin antibodies; the last panel was blotted with anti-WDR76 and anti- HaloTag™, which was not detected because of the cleavage during elution. (C) Topological data analysis was performed on 164 proteins with a Z-score greater than 2 in WDR76 and at least one histone purification compared to controls. All the nodes in the network are colored based on metric PCA coordinate 2. Filters with variance normalized Euclidean metric were used (resolution 30, gain 3.0x).
Magnetic Labels (Magneto Enzyme), supplied by Magna Biosciences, 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/result/magnetic labels (magneto-enzyme)/product/Magna Biosciences
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magnetic labels (magneto-enzyme) - by Bioz Stars, 2026-05
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anisotropic magneto-resistive (amr) magnetic sensor  (MemSic Inc)
90
MemSic Inc anisotropic magneto-resistive (amr) magnetic sensor
(A) Heat map of relative abundance of 40 proteins shared between WDR76 and histones. The color intensity represents protein abundance with bright yellow displaying highest abundance (average distributed spectral counts) and black indicates that the protein was not detected in a particular purification. (B) Western blots of inputs and purifications from Halo-WDR76 stable cell line or HEK293FRT parental cell line shows that PARP1 and XRCC5 can be co-purified with WDR76, which is consistent with the proteomics analysis. Lane 1 and 2 are whole cell lysates from Halo-WDR76 stable cell line or HEK293FRT cells. Lane 3 and 4 are the protein purified with <t>HaloTag™</t> magnetic beads from Halo-WDR76 stable cell line or HEK293FRT cells. The top panel was blotted with anti-PARP1 and anti-Actin antibodies; the middle panel was blotted with anti-XRCC5 and anti-Actin antibodies; the last panel was blotted with anti-WDR76 and anti- HaloTag™, which was not detected because of the cleavage during elution. (C) Topological data analysis was performed on 164 proteins with a Z-score greater than 2 in WDR76 and at least one histone purification compared to controls. All the nodes in the network are colored based on metric PCA coordinate 2. Filters with variance normalized Euclidean metric were used (resolution 30, gain 3.0x).
Anisotropic Magneto Resistive (Amr) Magnetic Sensor, supplied by MemSic 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/result/anisotropic magneto-resistive (amr) magnetic sensor/product/MemSic Inc
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anisotropic magneto-resistive (amr) magnetic sensor - by Bioz Stars, 2026-05
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large acceptance magnex magnetic spectrometer  (Magnex Scientific Limited)
86
Magnex Scientific Limited large acceptance magnex magnetic spectrometer
(A) Heat map of relative abundance of 40 proteins shared between WDR76 and histones. The color intensity represents protein abundance with bright yellow displaying highest abundance (average distributed spectral counts) and black indicates that the protein was not detected in a particular purification. (B) Western blots of inputs and purifications from Halo-WDR76 stable cell line or HEK293FRT parental cell line shows that PARP1 and XRCC5 can be co-purified with WDR76, which is consistent with the proteomics analysis. Lane 1 and 2 are whole cell lysates from Halo-WDR76 stable cell line or HEK293FRT cells. Lane 3 and 4 are the protein purified with <t>HaloTag™</t> magnetic beads from Halo-WDR76 stable cell line or HEK293FRT cells. The top panel was blotted with anti-PARP1 and anti-Actin antibodies; the middle panel was blotted with anti-XRCC5 and anti-Actin antibodies; the last panel was blotted with anti-WDR76 and anti- HaloTag™, which was not detected because of the cleavage during elution. (C) Topological data analysis was performed on 164 proteins with a Z-score greater than 2 in WDR76 and at least one histone purification compared to controls. All the nodes in the network are colored based on metric PCA coordinate 2. Filters with variance normalized Euclidean metric were used (resolution 30, gain 3.0x).
Large Acceptance Magnex Magnetic Spectrometer, supplied by Magnex Scientific Limited, 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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large acceptance magnex magnetic spectrometer - by Bioz Stars, 2026-05
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polar magnetooptic kerr effect (moke) apparatus  (Durham Magneto Optics Ltd)
90
Durham Magneto Optics Ltd polar magnetooptic kerr effect (moke) apparatus
(A) Heat map of relative abundance of 40 proteins shared between WDR76 and histones. The color intensity represents protein abundance with bright yellow displaying highest abundance (average distributed spectral counts) and black indicates that the protein was not detected in a particular purification. (B) Western blots of inputs and purifications from Halo-WDR76 stable cell line or HEK293FRT parental cell line shows that PARP1 and XRCC5 can be co-purified with WDR76, which is consistent with the proteomics analysis. Lane 1 and 2 are whole cell lysates from Halo-WDR76 stable cell line or HEK293FRT cells. Lane 3 and 4 are the protein purified with <t>HaloTag™</t> magnetic beads from Halo-WDR76 stable cell line or HEK293FRT cells. The top panel was blotted with anti-PARP1 and anti-Actin antibodies; the middle panel was blotted with anti-XRCC5 and anti-Actin antibodies; the last panel was blotted with anti-WDR76 and anti- HaloTag™, which was not detected because of the cleavage during elution. (C) Topological data analysis was performed on 164 proteins with a Z-score greater than 2 in WDR76 and at least one histone purification compared to controls. All the nodes in the network are colored based on metric PCA coordinate 2. Filters with variance normalized Euclidean metric were used (resolution 30, gain 3.0x).
Polar Magnetooptic Kerr Effect (Moke) Apparatus, supplied by Durham Magneto Optics Ltd, 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/result/polar magnetooptic kerr effect (moke) apparatus/product/Durham Magneto Optics Ltd
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polar magnetooptic kerr effect (moke) apparatus - by Bioz Stars, 2026-05
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magnetic multilayer giant magneto-impedance sensor  (BioMimetic Therapeutics)
90
BioMimetic Therapeutics magnetic multilayer giant magneto-impedance sensor
(A) Heat map of relative abundance of 40 proteins shared between WDR76 and histones. The color intensity represents protein abundance with bright yellow displaying highest abundance (average distributed spectral counts) and black indicates that the protein was not detected in a particular purification. (B) Western blots of inputs and purifications from Halo-WDR76 stable cell line or HEK293FRT parental cell line shows that PARP1 and XRCC5 can be co-purified with WDR76, which is consistent with the proteomics analysis. Lane 1 and 2 are whole cell lysates from Halo-WDR76 stable cell line or HEK293FRT cells. Lane 3 and 4 are the protein purified with <t>HaloTag™</t> magnetic beads from Halo-WDR76 stable cell line or HEK293FRT cells. The top panel was blotted with anti-PARP1 and anti-Actin antibodies; the middle panel was blotted with anti-XRCC5 and anti-Actin antibodies; the last panel was blotted with anti-WDR76 and anti- HaloTag™, which was not detected because of the cleavage during elution. (C) Topological data analysis was performed on 164 proteins with a Z-score greater than 2 in WDR76 and at least one histone purification compared to controls. All the nodes in the network are colored based on metric PCA coordinate 2. Filters with variance normalized Euclidean metric were used (resolution 30, gain 3.0x).
Magnetic Multilayer Giant Magneto Impedance Sensor, supplied by BioMimetic Therapeutics, 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/result/magnetic multilayer giant magneto-impedance sensor/product/BioMimetic Therapeutics
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magnetic multilayer giant magneto-impedance sensor - by Bioz Stars, 2026-05
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magnetic presentation device magnest  (CellSearch inc)
90
CellSearch inc magnetic presentation device magnest
(A) Heat map of relative abundance of 40 proteins shared between WDR76 and histones. The color intensity represents protein abundance with bright yellow displaying highest abundance (average distributed spectral counts) and black indicates that the protein was not detected in a particular purification. (B) Western blots of inputs and purifications from Halo-WDR76 stable cell line or HEK293FRT parental cell line shows that PARP1 and XRCC5 can be co-purified with WDR76, which is consistent with the proteomics analysis. Lane 1 and 2 are whole cell lysates from Halo-WDR76 stable cell line or HEK293FRT cells. Lane 3 and 4 are the protein purified with <t>HaloTag™</t> magnetic beads from Halo-WDR76 stable cell line or HEK293FRT cells. The top panel was blotted with anti-PARP1 and anti-Actin antibodies; the middle panel was blotted with anti-XRCC5 and anti-Actin antibodies; the last panel was blotted with anti-WDR76 and anti- HaloTag™, which was not detected because of the cleavage during elution. (C) Topological data analysis was performed on 164 proteins with a Z-score greater than 2 in WDR76 and at least one histone purification compared to controls. All the nodes in the network are colored based on metric PCA coordinate 2. Filters with variance normalized Euclidean metric were used (resolution 30, gain 3.0x).
Magnetic Presentation Device Magnest, supplied by CellSearch inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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magnetic presentation device magnest - by Bioz Stars, 2026-05
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protein g magnetic beads magnetm  (Promega)
90
Promega protein g magnetic beads magnetm
(A) Heat map of relative abundance of 40 proteins shared between WDR76 and histones. The color intensity represents protein abundance with bright yellow displaying highest abundance (average distributed spectral counts) and black indicates that the protein was not detected in a particular purification. (B) Western blots of inputs and purifications from Halo-WDR76 stable cell line or HEK293FRT parental cell line shows that PARP1 and XRCC5 can be co-purified with WDR76, which is consistent with the proteomics analysis. Lane 1 and 2 are whole cell lysates from Halo-WDR76 stable cell line or HEK293FRT cells. Lane 3 and 4 are the protein purified with <t>HaloTag™</t> magnetic beads from Halo-WDR76 stable cell line or HEK293FRT cells. The top panel was blotted with anti-PARP1 and anti-Actin antibodies; the middle panel was blotted with anti-XRCC5 and anti-Actin antibodies; the last panel was blotted with anti-WDR76 and anti- HaloTag™, which was not detected because of the cleavage during elution. (C) Topological data analysis was performed on 164 proteins with a Z-score greater than 2 in WDR76 and at least one histone purification compared to controls. All the nodes in the network are colored based on metric PCA coordinate 2. Filters with variance normalized Euclidean metric were used (resolution 30, gain 3.0x).
Protein G Magnetic Beads Magnetm, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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magnetic force microscope mfm  (attocube systems AG)
90
attocube systems AG magnetic force microscope mfm
(A) Heat map of relative abundance of 40 proteins shared between WDR76 and histones. The color intensity represents protein abundance with bright yellow displaying highest abundance (average distributed spectral counts) and black indicates that the protein was not detected in a particular purification. (B) Western blots of inputs and purifications from Halo-WDR76 stable cell line or HEK293FRT parental cell line shows that PARP1 and XRCC5 can be co-purified with WDR76, which is consistent with the proteomics analysis. Lane 1 and 2 are whole cell lysates from Halo-WDR76 stable cell line or HEK293FRT cells. Lane 3 and 4 are the protein purified with <t>HaloTag™</t> magnetic beads from Halo-WDR76 stable cell line or HEK293FRT cells. The top panel was blotted with anti-PARP1 and anti-Actin antibodies; the middle panel was blotted with anti-XRCC5 and anti-Actin antibodies; the last panel was blotted with anti-WDR76 and anti- HaloTag™, which was not detected because of the cleavage during elution. (C) Topological data analysis was performed on 164 proteins with a Z-score greater than 2 in WDR76 and at least one histone purification compared to controls. All the nodes in the network are colored based on metric PCA coordinate 2. Filters with variance normalized Euclidean metric were used (resolution 30, gain 3.0x).
Magnetic Force Microscope Mfm, supplied by attocube systems AG, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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magneto-rheological device (mrd) 170/1 t  (Anton Paar)
90
Anton Paar magneto-rheological device (mrd) 170/1 t
(A) Heat map of relative abundance of 40 proteins shared between WDR76 and histones. The color intensity represents protein abundance with bright yellow displaying highest abundance (average distributed spectral counts) and black indicates that the protein was not detected in a particular purification. (B) Western blots of inputs and purifications from Halo-WDR76 stable cell line or HEK293FRT parental cell line shows that PARP1 and XRCC5 can be co-purified with WDR76, which is consistent with the proteomics analysis. Lane 1 and 2 are whole cell lysates from Halo-WDR76 stable cell line or HEK293FRT cells. Lane 3 and 4 are the protein purified with <t>HaloTag™</t> magnetic beads from Halo-WDR76 stable cell line or HEK293FRT cells. The top panel was blotted with anti-PARP1 and anti-Actin antibodies; the middle panel was blotted with anti-XRCC5 and anti-Actin antibodies; the last panel was blotted with anti-WDR76 and anti- HaloTag™, which was not detected because of the cleavage during elution. (C) Topological data analysis was performed on 164 proteins with a Z-score greater than 2 in WDR76 and at least one histone purification compared to controls. All the nodes in the network are colored based on metric PCA coordinate 2. Filters with variance normalized Euclidean metric were used (resolution 30, gain 3.0x).
Magneto Rheological Device (Mrd) 170/1 T, supplied by Anton Paar, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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magneto-rheological device (mrd) 170/1 t - by Bioz Stars, 2026-05
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magneto-optical microscope polar magneto-optical kerr microscope  (Evico Magnetics)
90
Evico Magnetics magneto-optical microscope polar magneto-optical kerr microscope
(A) Heat map of relative abundance of 40 proteins shared between WDR76 and histones. The color intensity represents protein abundance with bright yellow displaying highest abundance (average distributed spectral counts) and black indicates that the protein was not detected in a particular purification. (B) Western blots of inputs and purifications from Halo-WDR76 stable cell line or HEK293FRT parental cell line shows that PARP1 and XRCC5 can be co-purified with WDR76, which is consistent with the proteomics analysis. Lane 1 and 2 are whole cell lysates from Halo-WDR76 stable cell line or HEK293FRT cells. Lane 3 and 4 are the protein purified with <t>HaloTag™</t> magnetic beads from Halo-WDR76 stable cell line or HEK293FRT cells. The top panel was blotted with anti-PARP1 and anti-Actin antibodies; the middle panel was blotted with anti-XRCC5 and anti-Actin antibodies; the last panel was blotted with anti-WDR76 and anti- HaloTag™, which was not detected because of the cleavage during elution. (C) Topological data analysis was performed on 164 proteins with a Z-score greater than 2 in WDR76 and at least one histone purification compared to controls. All the nodes in the network are colored based on metric PCA coordinate 2. Filters with variance normalized Euclidean metric were used (resolution 30, gain 3.0x).
Magneto Optical Microscope Polar Magneto Optical Kerr Microscope, supplied by Evico Magnetics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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magneto-optical microscope polar magneto-optical kerr microscope - by Bioz Stars, 2026-05
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magneto-optical kerr microscope  (Evico Magnetics)
90
Evico Magnetics magneto-optical kerr microscope
(A) Heat map of relative abundance of 40 proteins shared between WDR76 and histones. The color intensity represents protein abundance with bright yellow displaying highest abundance (average distributed spectral counts) and black indicates that the protein was not detected in a particular purification. (B) Western blots of inputs and purifications from Halo-WDR76 stable cell line or HEK293FRT parental cell line shows that PARP1 and XRCC5 can be co-purified with WDR76, which is consistent with the proteomics analysis. Lane 1 and 2 are whole cell lysates from Halo-WDR76 stable cell line or HEK293FRT cells. Lane 3 and 4 are the protein purified with <t>HaloTag™</t> magnetic beads from Halo-WDR76 stable cell line or HEK293FRT cells. The top panel was blotted with anti-PARP1 and anti-Actin antibodies; the middle panel was blotted with anti-XRCC5 and anti-Actin antibodies; the last panel was blotted with anti-WDR76 and anti- HaloTag™, which was not detected because of the cleavage during elution. (C) Topological data analysis was performed on 164 proteins with a Z-score greater than 2 in WDR76 and at least one histone purification compared to controls. All the nodes in the network are colored based on metric PCA coordinate 2. Filters with variance normalized Euclidean metric were used (resolution 30, gain 3.0x).
Magneto Optical Kerr Microscope, supplied by Evico Magnetics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


(A) Heat map of relative abundance of 40 proteins shared between WDR76 and histones. The color intensity represents protein abundance with bright yellow displaying highest abundance (average distributed spectral counts) and black indicates that the protein was not detected in a particular purification. (B) Western blots of inputs and purifications from Halo-WDR76 stable cell line or HEK293FRT parental cell line shows that PARP1 and XRCC5 can be co-purified with WDR76, which is consistent with the proteomics analysis. Lane 1 and 2 are whole cell lysates from Halo-WDR76 stable cell line or HEK293FRT cells. Lane 3 and 4 are the protein purified with HaloTag™ magnetic beads from Halo-WDR76 stable cell line or HEK293FRT cells. The top panel was blotted with anti-PARP1 and anti-Actin antibodies; the middle panel was blotted with anti-XRCC5 and anti-Actin antibodies; the last panel was blotted with anti-WDR76 and anti- HaloTag™, which was not detected because of the cleavage during elution. (C) Topological data analysis was performed on 164 proteins with a Z-score greater than 2 in WDR76 and at least one histone purification compared to controls. All the nodes in the network are colored based on metric PCA coordinate 2. Filters with variance normalized Euclidean metric were used (resolution 30, gain 3.0x).

Journal: PLoS ONE

Article Title: WDR76 Co-Localizes with Heterochromatin Related Proteins and Rapidly Responds to DNA Damage

doi: 10.1371/journal.pone.0155492

Figure Lengend Snippet: (A) Heat map of relative abundance of 40 proteins shared between WDR76 and histones. The color intensity represents protein abundance with bright yellow displaying highest abundance (average distributed spectral counts) and black indicates that the protein was not detected in a particular purification. (B) Western blots of inputs and purifications from Halo-WDR76 stable cell line or HEK293FRT parental cell line shows that PARP1 and XRCC5 can be co-purified with WDR76, which is consistent with the proteomics analysis. Lane 1 and 2 are whole cell lysates from Halo-WDR76 stable cell line or HEK293FRT cells. Lane 3 and 4 are the protein purified with HaloTag™ magnetic beads from Halo-WDR76 stable cell line or HEK293FRT cells. The top panel was blotted with anti-PARP1 and anti-Actin antibodies; the middle panel was blotted with anti-XRCC5 and anti-Actin antibodies; the last panel was blotted with anti-WDR76 and anti- HaloTag™, which was not detected because of the cleavage during elution. (C) Topological data analysis was performed on 164 proteins with a Z-score greater than 2 in WDR76 and at least one histone purification compared to controls. All the nodes in the network are colored based on metric PCA coordinate 2. Filters with variance normalized Euclidean metric were used (resolution 30, gain 3.0x).

Article Snippet: MagneTM HaloTag ® magnetic affinity beads and HaloTagTMTMRDirect ligand were purchased from Promega (Madison, WI).

Techniques: Quantitative Proteomics, Purification, Western Blot, Stable Transfection, Magnetic Beads

Cells stably expressing Halo-WDR76 were separately transiently transfected with CLIPtag™-FLAG proteins and HaloTag™ protein purifications conducted. Western blotting for tubulin was used as a loading control and western blotting with an anti-FLAG antibody was used to detect CBX1 (A), CBX3 (B), and CBX5 (C). Both the inputs and the results of the pulldown is shown. (D) Cells stably expressing Halo-WDR76 were transiently transfected with CLIPg™-FLAG construct to demonstrate that this construct was not responsible for the co-purifications of CBX proteins with WDR76.

Journal: PLoS ONE

Article Title: WDR76 Co-Localizes with Heterochromatin Related Proteins and Rapidly Responds to DNA Damage

doi: 10.1371/journal.pone.0155492

Figure Lengend Snippet: Cells stably expressing Halo-WDR76 were separately transiently transfected with CLIPtag™-FLAG proteins and HaloTag™ protein purifications conducted. Western blotting for tubulin was used as a loading control and western blotting with an anti-FLAG antibody was used to detect CBX1 (A), CBX3 (B), and CBX5 (C). Both the inputs and the results of the pulldown is shown. (D) Cells stably expressing Halo-WDR76 were transiently transfected with CLIPg™-FLAG construct to demonstrate that this construct was not responsible for the co-purifications of CBX proteins with WDR76.

Article Snippet: MagneTM HaloTag ® magnetic affinity beads and HaloTagTMTMRDirect ligand were purchased from Promega (Madison, WI).

Techniques: Stable Transfection, Expressing, Transfection, Western Blot, Control, Construct