internal reflection fluorescence microscope Search Results


96
Nikon prism type total internal reflection fluorescence tirf microscope
Prism Type Total Internal Reflection Fluorescence Tirf Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/internal+reflection+fluorescence+microscope/10__1074_slash_jbc__ra117__001143-152-10-18?v=Nikon
Average 96 stars, based on 1 article reviews
prism type total internal reflection fluorescence tirf microscope - by Bioz Stars, 2026-08
96/100 stars
  Buy from Supplier

94
Nikon total internal reflection fluorescence tirf microscopes
Large-conductance Ca2+-activated K+ channel α-subunit (BKα) and BKγ1 form molecular complex on the cell surface in mouse bronchial smooth muscle cells (mBSMCs). A: coimmunoprecipitation assay was performed using rat BSMs (rBSMs). Lysates were precipitated with anti-BKα antibody and blotted using either anti-BKα or anti-BKγ1 antibody. Similar results were obtained from 3 independent experiments. Two rats were used for each experiment. Lane 1, lysates from rBSM; lane 2, samples precipitated with control resin that cannot bind to antibodies; lane 3, samples precipitated with resin that binds to anti-BKα antibody. B: <t>total</t> <t>internal</t> <t>reflection</t> fluorescence <t>(TIRF)</t> imaging of mBSMCs, in which BKα and BKγ1 were labeled with each antibody. Fluorescent signals from particles corresponding to BKα, BKγ1, and colocalization are shown in green, red, and yellow, respectively. Merged image was overlapped with a cell image. C: ratio of BKα particles localized alone or colocalized with BKγ1 to total BKα particles in mBSMCs (BKα alone, 134 particles and colocalized, 214 particles from 15 cells).
Total Internal Reflection Fluorescence Tirf Microscopes, supplied by Nikon, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/internal+reflection+fluorescence+microscope/pmc07052682-93-13-19?v=Nikon
Average 94 stars, based on 1 article reviews
total internal reflection fluorescence tirf microscopes - by Bioz Stars, 2026-08
94/100 stars
  Buy from Supplier

90
Photon Technology International Inc ratio-based microscopic fluorescent spectrophotometer
Large-conductance Ca2+-activated K+ channel α-subunit (BKα) and BKγ1 form molecular complex on the cell surface in mouse bronchial smooth muscle cells (mBSMCs). A: coimmunoprecipitation assay was performed using rat BSMs (rBSMs). Lysates were precipitated with anti-BKα antibody and blotted using either anti-BKα or anti-BKγ1 antibody. Similar results were obtained from 3 independent experiments. Two rats were used for each experiment. Lane 1, lysates from rBSM; lane 2, samples precipitated with control resin that cannot bind to antibodies; lane 3, samples precipitated with resin that binds to anti-BKα antibody. B: <t>total</t> <t>internal</t> <t>reflection</t> fluorescence <t>(TIRF)</t> imaging of mBSMCs, in which BKα and BKγ1 were labeled with each antibody. Fluorescent signals from particles corresponding to BKα, BKγ1, and colocalization are shown in green, red, and yellow, respectively. Merged image was overlapped with a cell image. C: ratio of BKα particles localized alone or colocalized with BKγ1 to total BKα particles in mBSMCs (BKα alone, 134 particles and colocalized, 214 particles from 15 cells).
Ratio Based Microscopic Fluorescent Spectrophotometer, supplied by Photon Technology International 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/internal+reflection+fluorescence+microscope/pm11316737-104-3-5?v=Photon+Technology+International+Inc
Average 90 stars, based on 1 article reviews
ratio-based microscopic fluorescent spectrophotometer - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier

90
TEM Messtechnik scanning fluorescence microscope with a cassegrain-type reflective objective (co)
Large-conductance Ca2+-activated K+ channel α-subunit (BKα) and BKγ1 form molecular complex on the cell surface in mouse bronchial smooth muscle cells (mBSMCs). A: coimmunoprecipitation assay was performed using rat BSMs (rBSMs). Lysates were precipitated with anti-BKα antibody and blotted using either anti-BKα or anti-BKγ1 antibody. Similar results were obtained from 3 independent experiments. Two rats were used for each experiment. Lane 1, lysates from rBSM; lane 2, samples precipitated with control resin that cannot bind to antibodies; lane 3, samples precipitated with resin that binds to anti-BKα antibody. B: <t>total</t> <t>internal</t> <t>reflection</t> fluorescence <t>(TIRF)</t> imaging of mBSMCs, in which BKα and BKγ1 were labeled with each antibody. Fluorescent signals from particles corresponding to BKα, BKγ1, and colocalization are shown in green, red, and yellow, respectively. Merged image was overlapped with a cell image. C: ratio of BKα particles localized alone or colocalized with BKγ1 to total BKα particles in mBSMCs (BKα alone, 134 particles and colocalized, 214 particles from 15 cells).
Scanning Fluorescence Microscope With A Cassegrain Type Reflective Objective (Co), supplied by TEM Messtechnik, 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/internal+reflection+fluorescence+microscope/pm31779407-58-17-44?v=TEM+Messtechnik
Average 90 stars, based on 1 article reviews
scanning fluorescence microscope with a cassegrain-type reflective objective (co) - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier

90
TIRF Technologies Inc injector from the lightguide-based total internal reflection fluorescence microscope
Large-conductance Ca2+-activated K+ channel α-subunit (BKα) and BKγ1 form molecular complex on the cell surface in mouse bronchial smooth muscle cells (mBSMCs). A: coimmunoprecipitation assay was performed using rat BSMs (rBSMs). Lysates were precipitated with anti-BKα antibody and blotted using either anti-BKα or anti-BKγ1 antibody. Similar results were obtained from 3 independent experiments. Two rats were used for each experiment. Lane 1, lysates from rBSM; lane 2, samples precipitated with control resin that cannot bind to antibodies; lane 3, samples precipitated with resin that binds to anti-BKα antibody. B: <t>total</t> <t>internal</t> <t>reflection</t> fluorescence <t>(TIRF)</t> imaging of mBSMCs, in which BKα and BKγ1 were labeled with each antibody. Fluorescent signals from particles corresponding to BKα, BKγ1, and colocalization are shown in green, red, and yellow, respectively. Merged image was overlapped with a cell image. C: ratio of BKα particles localized alone or colocalized with BKγ1 to total BKα particles in mBSMCs (BKα alone, 134 particles and colocalized, 214 particles from 15 cells).
Injector From The Lightguide Based Total Internal Reflection Fluorescence Microscope, supplied by TIRF Technologies 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/internal+reflection+fluorescence+microscope/10__1080_slash_15421406__2016__1146861-69-1-11?v=TIRF+Technologies+Inc
Average 90 stars, based on 1 article reviews
injector from the lightguide-based total internal reflection fluorescence microscope - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier

90
Photon Technology International Inc ratiobased microscopic fluorescent spectrophotometer
Large-conductance Ca2+-activated K+ channel α-subunit (BKα) and BKγ1 form molecular complex on the cell surface in mouse bronchial smooth muscle cells (mBSMCs). A: coimmunoprecipitation assay was performed using rat BSMs (rBSMs). Lysates were precipitated with anti-BKα antibody and blotted using either anti-BKα or anti-BKγ1 antibody. Similar results were obtained from 3 independent experiments. Two rats were used for each experiment. Lane 1, lysates from rBSM; lane 2, samples precipitated with control resin that cannot bind to antibodies; lane 3, samples precipitated with resin that binds to anti-BKα antibody. B: <t>total</t> <t>internal</t> <t>reflection</t> fluorescence <t>(TIRF)</t> imaging of mBSMCs, in which BKα and BKγ1 were labeled with each antibody. Fluorescent signals from particles corresponding to BKα, BKγ1, and colocalization are shown in green, red, and yellow, respectively. Merged image was overlapped with a cell image. C: ratio of BKα particles localized alone or colocalized with BKγ1 to total BKα particles in mBSMCs (BKα alone, 134 particles and colocalized, 214 particles from 15 cells).
Ratiobased Microscopic Fluorescent Spectrophotometer, supplied by Photon Technology International 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/internal+reflection+fluorescence+microscope/pm18574677-107-1-5?v=Photon+Technology+International+Inc
Average 90 stars, based on 1 article reviews
ratiobased microscopic fluorescent spectrophotometer - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier

90
Photon Technology International Inc tm-50 microscope-based fluorescence lifetime spectrofluorometer model gl-3300
Large-conductance Ca2+-activated K+ channel α-subunit (BKα) and BKγ1 form molecular complex on the cell surface in mouse bronchial smooth muscle cells (mBSMCs). A: coimmunoprecipitation assay was performed using rat BSMs (rBSMs). Lysates were precipitated with anti-BKα antibody and blotted using either anti-BKα or anti-BKγ1 antibody. Similar results were obtained from 3 independent experiments. Two rats were used for each experiment. Lane 1, lysates from rBSM; lane 2, samples precipitated with control resin that cannot bind to antibodies; lane 3, samples precipitated with resin that binds to anti-BKα antibody. B: <t>total</t> <t>internal</t> <t>reflection</t> fluorescence <t>(TIRF)</t> imaging of mBSMCs, in which BKα and BKγ1 were labeled with each antibody. Fluorescent signals from particles corresponding to BKα, BKγ1, and colocalization are shown in green, red, and yellow, respectively. Merged image was overlapped with a cell image. C: ratio of BKα particles localized alone or colocalized with BKγ1 to total BKα particles in mBSMCs (BKα alone, 134 particles and colocalized, 214 particles from 15 cells).
Tm 50 Microscope Based Fluorescence Lifetime Spectrofluorometer Model Gl 3300, supplied by Photon Technology International 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/internal+reflection+fluorescence+microscope/pm35638714-150-37-42?v=Photon+Technology+International+Inc
Average 90 stars, based on 1 article reviews
tm-50 microscope-based fluorescence lifetime spectrofluorometer model gl-3300 - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier

90
Photon Technology International Inc fluorescence microscope with fdim system
Large-conductance Ca2+-activated K+ channel α-subunit (BKα) and BKγ1 form molecular complex on the cell surface in mouse bronchial smooth muscle cells (mBSMCs). A: coimmunoprecipitation assay was performed using rat BSMs (rBSMs). Lysates were precipitated with anti-BKα antibody and blotted using either anti-BKα or anti-BKγ1 antibody. Similar results were obtained from 3 independent experiments. Two rats were used for each experiment. Lane 1, lysates from rBSM; lane 2, samples precipitated with control resin that cannot bind to antibodies; lane 3, samples precipitated with resin that binds to anti-BKα antibody. B: <t>total</t> <t>internal</t> <t>reflection</t> fluorescence <t>(TIRF)</t> imaging of mBSMCs, in which BKα and BKγ1 were labeled with each antibody. Fluorescent signals from particles corresponding to BKα, BKγ1, and colocalization are shown in green, red, and yellow, respectively. Merged image was overlapped with a cell image. C: ratio of BKα particles localized alone or colocalized with BKγ1 to total BKα particles in mBSMCs (BKα alone, 134 particles and colocalized, 214 particles from 15 cells).
Fluorescence Microscope With Fdim System, supplied by Photon Technology International 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/internal+reflection+fluorescence+microscope/pm23045045-522-37-39?v=Photon+Technology+International+Inc
Average 90 stars, based on 1 article reviews
fluorescence microscope with fdim system - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier

90
BioResource International Inc fluorescence microscope
Large-conductance Ca2+-activated K+ channel α-subunit (BKα) and BKγ1 form molecular complex on the cell surface in mouse bronchial smooth muscle cells (mBSMCs). A: coimmunoprecipitation assay was performed using rat BSMs (rBSMs). Lysates were precipitated with anti-BKα antibody and blotted using either anti-BKα or anti-BKγ1 antibody. Similar results were obtained from 3 independent experiments. Two rats were used for each experiment. Lane 1, lysates from rBSM; lane 2, samples precipitated with control resin that cannot bind to antibodies; lane 3, samples precipitated with resin that binds to anti-BKα antibody. B: <t>total</t> <t>internal</t> <t>reflection</t> fluorescence <t>(TIRF)</t> imaging of mBSMCs, in which BKα and BKγ1 were labeled with each antibody. Fluorescent signals from particles corresponding to BKα, BKγ1, and colocalization are shown in green, red, and yellow, respectively. Merged image was overlapped with a cell image. C: ratio of BKα particles localized alone or colocalized with BKγ1 to total BKα particles in mBSMCs (BKα alone, 134 particles and colocalized, 214 particles from 15 cells).
Fluorescence Microscope, supplied by BioResource International 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/internal+reflection+fluorescence+microscope/pm15752045-263-8-19?v=BioResource+International+Inc
Average 90 stars, based on 1 article reviews
fluorescence microscope - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier

Image Search Results


Large-conductance Ca2+-activated K+ channel α-subunit (BKα) and BKγ1 form molecular complex on the cell surface in mouse bronchial smooth muscle cells (mBSMCs). A: coimmunoprecipitation assay was performed using rat BSMs (rBSMs). Lysates were precipitated with anti-BKα antibody and blotted using either anti-BKα or anti-BKγ1 antibody. Similar results were obtained from 3 independent experiments. Two rats were used for each experiment. Lane 1, lysates from rBSM; lane 2, samples precipitated with control resin that cannot bind to antibodies; lane 3, samples precipitated with resin that binds to anti-BKα antibody. B: total internal reflection fluorescence (TIRF) imaging of mBSMCs, in which BKα and BKγ1 were labeled with each antibody. Fluorescent signals from particles corresponding to BKα, BKγ1, and colocalization are shown in green, red, and yellow, respectively. Merged image was overlapped with a cell image. C: ratio of BKα particles localized alone or colocalized with BKγ1 to total BKα particles in mBSMCs (BKα alone, 134 particles and colocalized, 214 particles from 15 cells).

Journal: American Journal of Physiology - Lung Cellular and Molecular Physiology

Article Title: Roles of LRRC26 as an auxiliary γ1-subunit of large-conductance Ca 2+ -activated K + channels in bronchial smooth muscle cells

doi: 10.1152/ajplung.00331.2019

Figure Lengend Snippet: Large-conductance Ca2+-activated K+ channel α-subunit (BKα) and BKγ1 form molecular complex on the cell surface in mouse bronchial smooth muscle cells (mBSMCs). A: coimmunoprecipitation assay was performed using rat BSMs (rBSMs). Lysates were precipitated with anti-BKα antibody and blotted using either anti-BKα or anti-BKγ1 antibody. Similar results were obtained from 3 independent experiments. Two rats were used for each experiment. Lane 1, lysates from rBSM; lane 2, samples precipitated with control resin that cannot bind to antibodies; lane 3, samples precipitated with resin that binds to anti-BKα antibody. B: total internal reflection fluorescence (TIRF) imaging of mBSMCs, in which BKα and BKγ1 were labeled with each antibody. Fluorescent signals from particles corresponding to BKα, BKγ1, and colocalization are shown in green, red, and yellow, respectively. Merged image was overlapped with a cell image. C: ratio of BKα particles localized alone or colocalized with BKγ1 to total BKα particles in mBSMCs (BKα alone, 134 particles and colocalized, 214 particles from 15 cells).

Article Snippet: Fluorescently labeled cells were observed by using confocal (AIR, Nikon, Tokyo, Japan) or total internal reflection fluorescence (TIRF) microscopes (Nikon).

Techniques: Co-Immunoprecipitation Assay, Fluorescence, Imaging, Labeling