prestained molecular weight protein standards Search Results


92
Danaher Inc anti jph2
<t>Jph2</t> knockdown has no effect on Ca 2+ spark frequency, amplitude, or kinetics. ( A ) Representative confocal Ca 2+ images of pressurized (60 mmHg), Fluo-4-AM–loaded cerebral arteries treated with control or Jph2 -targeting morpholinos. Colored boxes show selected ROIs where Ca 2+ sparks occurred. (Scale bar, 10 µm.) ( B ) Representative changes in fractional fluorescence ( F / F 0 ) as a function of time for ROIs in A . The trace color corresponds to the color of the respective ROI box. ( C ) Summary data showing the Ca 2+ spark frequency (in Hertz) normalized to surface area (in Hertz per 100 square micrometers) in cerebral arteries ( n = 5 to 6 cerebral arteries/group from 4 animals), as well as the amplitude ( F / F 0 ), half-duration [half-time ( t 1/2 ), in seconds], rise time ( t 1/2 , in seconds), and decay time ( t 1/2 , in seconds) of individual Ca 2+ spark events recorded from each group ( n = 616 events for control, n = 601 events for Jph2 -targeted). There were no significant differences.
Anti Jph2, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Sangon Biotech turecolor two-color pre-stained protein marker (10 kda–250 kda)
<t>Jph2</t> knockdown has no effect on Ca 2+ spark frequency, amplitude, or kinetics. ( A ) Representative confocal Ca 2+ images of pressurized (60 mmHg), Fluo-4-AM–loaded cerebral arteries treated with control or Jph2 -targeting morpholinos. Colored boxes show selected ROIs where Ca 2+ sparks occurred. (Scale bar, 10 µm.) ( B ) Representative changes in fractional fluorescence ( F / F 0 ) as a function of time for ROIs in A . The trace color corresponds to the color of the respective ROI box. ( C ) Summary data showing the Ca 2+ spark frequency (in Hertz) normalized to surface area (in Hertz per 100 square micrometers) in cerebral arteries ( n = 5 to 6 cerebral arteries/group from 4 animals), as well as the amplitude ( F / F 0 ), half-duration [half-time ( t 1/2 ), in seconds], rise time ( t 1/2 , in seconds), and decay time ( t 1/2 , in seconds) of individual Ca 2+ spark events recorded from each group ( n = 616 events for control, n = 601 events for Jph2 -targeted). There were no significant differences.
Turecolor Two Color Pre Stained Protein Marker (10 Kda–250 Kda), supplied by Sangon Biotech, 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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Fisher Scientific pre-stained molecular weight ladder pageruler plus prestained protein ladder 10-250kda
<t>Jph2</t> knockdown has no effect on Ca 2+ spark frequency, amplitude, or kinetics. ( A ) Representative confocal Ca 2+ images of pressurized (60 mmHg), Fluo-4-AM–loaded cerebral arteries treated with control or Jph2 -targeting morpholinos. Colored boxes show selected ROIs where Ca 2+ sparks occurred. (Scale bar, 10 µm.) ( B ) Representative changes in fractional fluorescence ( F / F 0 ) as a function of time for ROIs in A . The trace color corresponds to the color of the respective ROI box. ( C ) Summary data showing the Ca 2+ spark frequency (in Hertz) normalized to surface area (in Hertz per 100 square micrometers) in cerebral arteries ( n = 5 to 6 cerebral arteries/group from 4 animals), as well as the amplitude ( F / F 0 ), half-duration [half-time ( t 1/2 ), in seconds], rise time ( t 1/2 , in seconds), and decay time ( t 1/2 , in seconds) of individual Ca 2+ spark events recorded from each group ( n = 616 events for control, n = 601 events for Jph2 -targeted). There were no significant differences.
Pre Stained Molecular Weight Ladder Pageruler Plus Prestained Protein Ladder 10 250kda, supplied by Fisher Scientific, 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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Fluka Chemical prestained molecular weight protein standards
<t>Jph2</t> knockdown has no effect on Ca 2+ spark frequency, amplitude, or kinetics. ( A ) Representative confocal Ca 2+ images of pressurized (60 mmHg), Fluo-4-AM–loaded cerebral arteries treated with control or Jph2 -targeting morpholinos. Colored boxes show selected ROIs where Ca 2+ sparks occurred. (Scale bar, 10 µm.) ( B ) Representative changes in fractional fluorescence ( F / F 0 ) as a function of time for ROIs in A . The trace color corresponds to the color of the respective ROI box. ( C ) Summary data showing the Ca 2+ spark frequency (in Hertz) normalized to surface area (in Hertz per 100 square micrometers) in cerebral arteries ( n = 5 to 6 cerebral arteries/group from 4 animals), as well as the amplitude ( F / F 0 ), half-duration [half-time ( t 1/2 ), in seconds], rise time ( t 1/2 , in seconds), and decay time ( t 1/2 , in seconds) of individual Ca 2+ spark events recorded from each group ( n = 616 events for control, n = 601 events for Jph2 -targeted). There were no significant differences.
Prestained Molecular Weight Protein Standards, supplied by Fluka Chemical, 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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GenDEPOT broad-range prestained protein marker
<t>Jph2</t> knockdown has no effect on Ca 2+ spark frequency, amplitude, or kinetics. ( A ) Representative confocal Ca 2+ images of pressurized (60 mmHg), Fluo-4-AM–loaded cerebral arteries treated with control or Jph2 -targeting morpholinos. Colored boxes show selected ROIs where Ca 2+ sparks occurred. (Scale bar, 10 µm.) ( B ) Representative changes in fractional fluorescence ( F / F 0 ) as a function of time for ROIs in A . The trace color corresponds to the color of the respective ROI box. ( C ) Summary data showing the Ca 2+ spark frequency (in Hertz) normalized to surface area (in Hertz per 100 square micrometers) in cerebral arteries ( n = 5 to 6 cerebral arteries/group from 4 animals), as well as the amplitude ( F / F 0 ), half-duration [half-time ( t 1/2 ), in seconds], rise time ( t 1/2 , in seconds), and decay time ( t 1/2 , in seconds) of individual Ca 2+ spark events recorded from each group ( n = 616 events for control, n = 601 events for Jph2 -targeted). There were no significant differences.
Broad Range Prestained Protein Marker, supplied by GenDEPOT, 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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90
Beyotime protein marker p0068
<t>Jph2</t> knockdown has no effect on Ca 2+ spark frequency, amplitude, or kinetics. ( A ) Representative confocal Ca 2+ images of pressurized (60 mmHg), Fluo-4-AM–loaded cerebral arteries treated with control or Jph2 -targeting morpholinos. Colored boxes show selected ROIs where Ca 2+ sparks occurred. (Scale bar, 10 µm.) ( B ) Representative changes in fractional fluorescence ( F / F 0 ) as a function of time for ROIs in A . The trace color corresponds to the color of the respective ROI box. ( C ) Summary data showing the Ca 2+ spark frequency (in Hertz) normalized to surface area (in Hertz per 100 square micrometers) in cerebral arteries ( n = 5 to 6 cerebral arteries/group from 4 animals), as well as the amplitude ( F / F 0 ), half-duration [half-time ( t 1/2 ), in seconds], rise time ( t 1/2 , in seconds), and decay time ( t 1/2 , in seconds) of individual Ca 2+ spark events recorded from each group ( n = 616 events for control, n = 601 events for Jph2 -targeted). There were no significant differences.
Protein Marker P0068, supplied by Beyotime, 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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90
Promega prestained protein molecular weight marker
<t>Jph2</t> knockdown has no effect on Ca 2+ spark frequency, amplitude, or kinetics. ( A ) Representative confocal Ca 2+ images of pressurized (60 mmHg), Fluo-4-AM–loaded cerebral arteries treated with control or Jph2 -targeting morpholinos. Colored boxes show selected ROIs where Ca 2+ sparks occurred. (Scale bar, 10 µm.) ( B ) Representative changes in fractional fluorescence ( F / F 0 ) as a function of time for ROIs in A . The trace color corresponds to the color of the respective ROI box. ( C ) Summary data showing the Ca 2+ spark frequency (in Hertz) normalized to surface area (in Hertz per 100 square micrometers) in cerebral arteries ( n = 5 to 6 cerebral arteries/group from 4 animals), as well as the amplitude ( F / F 0 ), half-duration [half-time ( t 1/2 ), in seconds], rise time ( t 1/2 , in seconds), and decay time ( t 1/2 , in seconds) of individual Ca 2+ spark events recorded from each group ( n = 616 events for control, n = 601 events for Jph2 -targeted). There were no significant differences.
Prestained Protein Molecular Weight Marker, 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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90
Amersham Life Sciences Inc horseradish peroxidase-conjugated protein a, ecl kit, and rainbow prestained molecular weight marker
<t>Jph2</t> knockdown has no effect on Ca 2+ spark frequency, amplitude, or kinetics. ( A ) Representative confocal Ca 2+ images of pressurized (60 mmHg), Fluo-4-AM–loaded cerebral arteries treated with control or Jph2 -targeting morpholinos. Colored boxes show selected ROIs where Ca 2+ sparks occurred. (Scale bar, 10 µm.) ( B ) Representative changes in fractional fluorescence ( F / F 0 ) as a function of time for ROIs in A . The trace color corresponds to the color of the respective ROI box. ( C ) Summary data showing the Ca 2+ spark frequency (in Hertz) normalized to surface area (in Hertz per 100 square micrometers) in cerebral arteries ( n = 5 to 6 cerebral arteries/group from 4 animals), as well as the amplitude ( F / F 0 ), half-duration [half-time ( t 1/2 ), in seconds], rise time ( t 1/2 , in seconds), and decay time ( t 1/2 , in seconds) of individual Ca 2+ spark events recorded from each group ( n = 616 events for control, n = 601 events for Jph2 -targeted). There were no significant differences.
Horseradish Peroxidase Conjugated Protein A, Ecl Kit, And Rainbow Prestained Molecular Weight Marker, supplied by Amersham Life Sciences 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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Beyotime molecular weight protein standard prestained color protein ladder
<t>Jph2</t> knockdown has no effect on Ca 2+ spark frequency, amplitude, or kinetics. ( A ) Representative confocal Ca 2+ images of pressurized (60 mmHg), Fluo-4-AM–loaded cerebral arteries treated with control or Jph2 -targeting morpholinos. Colored boxes show selected ROIs where Ca 2+ sparks occurred. (Scale bar, 10 µm.) ( B ) Representative changes in fractional fluorescence ( F / F 0 ) as a function of time for ROIs in A . The trace color corresponds to the color of the respective ROI box. ( C ) Summary data showing the Ca 2+ spark frequency (in Hertz) normalized to surface area (in Hertz per 100 square micrometers) in cerebral arteries ( n = 5 to 6 cerebral arteries/group from 4 animals), as well as the amplitude ( F / F 0 ), half-duration [half-time ( t 1/2 ), in seconds], rise time ( t 1/2 , in seconds), and decay time ( t 1/2 , in seconds) of individual Ca 2+ spark events recorded from each group ( n = 616 events for control, n = 601 events for Jph2 -targeted). There were no significant differences.
Molecular Weight Protein Standard Prestained Color Protein Ladder, supplied by Beyotime, 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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Cleaver Scientific preserved molecular weight markers ladder blue wide range prestained protein ladder
<t>Jph2</t> knockdown has no effect on Ca 2+ spark frequency, amplitude, or kinetics. ( A ) Representative confocal Ca 2+ images of pressurized (60 mmHg), Fluo-4-AM–loaded cerebral arteries treated with control or Jph2 -targeting morpholinos. Colored boxes show selected ROIs where Ca 2+ sparks occurred. (Scale bar, 10 µm.) ( B ) Representative changes in fractional fluorescence ( F / F 0 ) as a function of time for ROIs in A . The trace color corresponds to the color of the respective ROI box. ( C ) Summary data showing the Ca 2+ spark frequency (in Hertz) normalized to surface area (in Hertz per 100 square micrometers) in cerebral arteries ( n = 5 to 6 cerebral arteries/group from 4 animals), as well as the amplitude ( F / F 0 ), half-duration [half-time ( t 1/2 ), in seconds], rise time ( t 1/2 , in seconds), and decay time ( t 1/2 , in seconds) of individual Ca 2+ spark events recorded from each group ( n = 616 events for control, n = 601 events for Jph2 -targeted). There were no significant differences.
Preserved Molecular Weight Markers Ladder Blue Wide Range Prestained Protein Ladder, supplied by Cleaver Scientific, 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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Beyotime protein molecular weight markers p0062
<t>Jph2</t> knockdown has no effect on Ca 2+ spark frequency, amplitude, or kinetics. ( A ) Representative confocal Ca 2+ images of pressurized (60 mmHg), Fluo-4-AM–loaded cerebral arteries treated with control or Jph2 -targeting morpholinos. Colored boxes show selected ROIs where Ca 2+ sparks occurred. (Scale bar, 10 µm.) ( B ) Representative changes in fractional fluorescence ( F / F 0 ) as a function of time for ROIs in A . The trace color corresponds to the color of the respective ROI box. ( C ) Summary data showing the Ca 2+ spark frequency (in Hertz) normalized to surface area (in Hertz per 100 square micrometers) in cerebral arteries ( n = 5 to 6 cerebral arteries/group from 4 animals), as well as the amplitude ( F / F 0 ), half-duration [half-time ( t 1/2 ), in seconds], rise time ( t 1/2 , in seconds), and decay time ( t 1/2 , in seconds) of individual Ca 2+ spark events recorded from each group ( n = 616 events for control, n = 601 events for Jph2 -targeted). There were no significant differences.
Protein Molecular Weight Markers P0062, supplied by Beyotime, 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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NEN Life Science prestained protein molecular weight markers
<t>Jph2</t> knockdown has no effect on Ca 2+ spark frequency, amplitude, or kinetics. ( A ) Representative confocal Ca 2+ images of pressurized (60 mmHg), Fluo-4-AM–loaded cerebral arteries treated with control or Jph2 -targeting morpholinos. Colored boxes show selected ROIs where Ca 2+ sparks occurred. (Scale bar, 10 µm.) ( B ) Representative changes in fractional fluorescence ( F / F 0 ) as a function of time for ROIs in A . The trace color corresponds to the color of the respective ROI box. ( C ) Summary data showing the Ca 2+ spark frequency (in Hertz) normalized to surface area (in Hertz per 100 square micrometers) in cerebral arteries ( n = 5 to 6 cerebral arteries/group from 4 animals), as well as the amplitude ( F / F 0 ), half-duration [half-time ( t 1/2 ), in seconds], rise time ( t 1/2 , in seconds), and decay time ( t 1/2 , in seconds) of individual Ca 2+ spark events recorded from each group ( n = 616 events for control, n = 601 events for Jph2 -targeted). There were no significant differences.
Prestained Protein Molecular Weight Markers, supplied by NEN Life Science, 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


Jph2 knockdown has no effect on Ca 2+ spark frequency, amplitude, or kinetics. ( A ) Representative confocal Ca 2+ images of pressurized (60 mmHg), Fluo-4-AM–loaded cerebral arteries treated with control or Jph2 -targeting morpholinos. Colored boxes show selected ROIs where Ca 2+ sparks occurred. (Scale bar, 10 µm.) ( B ) Representative changes in fractional fluorescence ( F / F 0 ) as a function of time for ROIs in A . The trace color corresponds to the color of the respective ROI box. ( C ) Summary data showing the Ca 2+ spark frequency (in Hertz) normalized to surface area (in Hertz per 100 square micrometers) in cerebral arteries ( n = 5 to 6 cerebral arteries/group from 4 animals), as well as the amplitude ( F / F 0 ), half-duration [half-time ( t 1/2 ), in seconds], rise time ( t 1/2 , in seconds), and decay time ( t 1/2 , in seconds) of individual Ca 2+ spark events recorded from each group ( n = 616 events for control, n = 601 events for Jph2 -targeted). There were no significant differences.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Article Title: Nanoscale coupling of junctophilin-2 and ryanodine receptors regulates vascular smooth muscle cell contractility

doi: 10.1073/pnas.1911304116

Figure Lengend Snippet: Jph2 knockdown has no effect on Ca 2+ spark frequency, amplitude, or kinetics. ( A ) Representative confocal Ca 2+ images of pressurized (60 mmHg), Fluo-4-AM–loaded cerebral arteries treated with control or Jph2 -targeting morpholinos. Colored boxes show selected ROIs where Ca 2+ sparks occurred. (Scale bar, 10 µm.) ( B ) Representative changes in fractional fluorescence ( F / F 0 ) as a function of time for ROIs in A . The trace color corresponds to the color of the respective ROI box. ( C ) Summary data showing the Ca 2+ spark frequency (in Hertz) normalized to surface area (in Hertz per 100 square micrometers) in cerebral arteries ( n = 5 to 6 cerebral arteries/group from 4 animals), as well as the amplitude ( F / F 0 ), half-duration [half-time ( t 1/2 ), in seconds], rise time ( t 1/2 , in seconds), and decay time ( t 1/2 , in seconds) of individual Ca 2+ spark events recorded from each group ( n = 616 events for control, n = 601 events for Jph2 -targeted). There were no significant differences.

Article Snippet: Rows were successively loaded with Wes antibody diluent blocking buffer; anti-JPH2 (ab116077; Abcam) or anti–β-actin (ab8227, Abcam) primary antibodies, diluted 1:20 and 1:1,500, respectively; horseradish peroxidase (HRP)-conjugated anti-rabbit secondary antibody (1×; ProteinSimple); and a luminol–peroxide mix.

Techniques: Fluorescence