scanr inverted microscope high content screening station Search Results


99
Yokogawa Electric csu10 spinning disk confocal scan head
Csu10 Spinning Disk Confocal Scan Head, supplied by Yokogawa Electric, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/scanr+inverted+microscope+high+content+screening+station/CSU-10/pmc05837070-163-23-29
Average 99 stars, based on 1 article reviews
csu10 spinning disk confocal scan head - by Bioz Stars, 2026-09
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99
Yokogawa Electric csu w1 spinning disk confocal scanning
Csu W1 Spinning Disk Confocal Scanning, supplied by Yokogawa Electric, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/scanr+inverted+microscope+high+content+screening+station/CSU-W1/pmc10312700-268-15-14
Average 99 stars, based on 1 article reviews
csu w1 spinning disk confocal scanning - by Bioz Stars, 2026-09
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Yokogawa Electric csu w1 sora confocal scanning
Csu W1 Sora Confocal Scanning, supplied by Yokogawa Electric, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ATCC hek293 cells
A Fluorescent images of tumor cells treated with TMTP1-DKK were examined with Confocal laser scanning microscopy. (a) PC-3M-1E8 cells (b) PC-3M-2B4 cells (c) MKN-45sci cells (d) NIH/3T3 cells. FITC-TMTP1-DKK (green) and control peptide were examined in xenograft tumors including PC-3M-1E8 (e)TMTP1-DKK, (f)svTMTP1-DKK, MKN-45sci (g) TMTP1-DKK, (h) svTMTP1-DKK. Nuclei were co-stained with DAPI (blue). B Fluorescent images of nomal cells (normal mammary epithelial cell MCF-10A, normal liver cell LO2 and <t>HEK293</t> cells) treated with TMTP1-DKK were examined with Confocal laser scanning microscopy. The morphological change of nomal cells was visualized using inverted microscope.
Hek293 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/scanr+inverted+microscope+high+content+screening+station/293/pmc03439480-148-21-27
Average 99 stars, based on 1 article reviews
hek293 cells - by Bioz Stars, 2026-09
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Nikon c1si spectral imaging confocal laser scanning system
A Fluorescent images of tumor cells treated with TMTP1-DKK were examined with Confocal laser scanning microscopy. (a) PC-3M-1E8 cells (b) PC-3M-2B4 cells (c) MKN-45sci cells (d) NIH/3T3 cells. FITC-TMTP1-DKK (green) and control peptide were examined in xenograft tumors including PC-3M-1E8 (e)TMTP1-DKK, (f)svTMTP1-DKK, MKN-45sci (g) TMTP1-DKK, (h) svTMTP1-DKK. Nuclei were co-stained with DAPI (blue). B Fluorescent images of nomal cells (normal mammary epithelial cell MCF-10A, normal liver cell LO2 and <t>HEK293</t> cells) treated with TMTP1-DKK were examined with Confocal laser scanning microscopy. The morphological change of nomal cells was visualized using inverted microscope.
C1si Spectral Imaging Confocal Laser Scanning System, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/scanr+inverted+microscope+high+content+screening+station/C2%2B/pm20490968-55-9-16
Average 99 stars, based on 1 article reviews
c1si spectral imaging confocal laser scanning system - by Bioz Stars, 2026-09
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KEYENCE inverted fluorescence slide scanning microscope keyence bz-x810
A Fluorescent images of tumor cells treated with TMTP1-DKK were examined with Confocal laser scanning microscopy. (a) PC-3M-1E8 cells (b) PC-3M-2B4 cells (c) MKN-45sci cells (d) NIH/3T3 cells. FITC-TMTP1-DKK (green) and control peptide were examined in xenograft tumors including PC-3M-1E8 (e)TMTP1-DKK, (f)svTMTP1-DKK, MKN-45sci (g) TMTP1-DKK, (h) svTMTP1-DKK. Nuclei were co-stained with DAPI (blue). B Fluorescent images of nomal cells (normal mammary epithelial cell MCF-10A, normal liver cell LO2 and <t>HEK293</t> cells) treated with TMTP1-DKK were examined with Confocal laser scanning microscopy. The morphological change of nomal cells was visualized using inverted microscope.
Inverted Fluorescence Slide Scanning Microscope Keyence Bz X810, supplied by KEYENCE, 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/scanr+inverted+microscope+high+content+screening+station/fluorescence+microscope+bz+9000/pm35124284-85-1-6
Average 90 stars, based on 1 article reviews
inverted fluorescence slide scanning microscope keyence bz-x810 - by Bioz Stars, 2026-09
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97
New England Biolabs mbp
(A) Western blot analyses of DDR proteins that co-immunoprecipitated with FLAG-HA-tagged MRI in WT and Ku70−/− abl pre-B cell nuclear extracts using anti-HA. (B) Schematic of sequential immunoprecipitations of MRI followed by Ku80 in cells expressing HA-MRI and FLAG-Ku80 (left). Western blot analyses of ATM, DNA-PKcs, Ku70, FLAG-Ku80, and HA-MRI from MRI−/− abl pre-B cell nuclear extract after first immunoprecipitation with anti-HA (Input HA IP) and following second immunoprecipitation with anti-FLAG or an IgG isotype control (right). (C) Western blot analyses of <t>purified</t> <t>recombinant</t> biotin-FLAG-ATM (bio-F-ATM) co-immunoprecipitated with 50 nM, 100 nM, or 200 nM of <t>MBP-tagged</t> human MRI, MRIΔN, and MRIΔC proteins. (D) Western blot analyses of DDR proteins that associated with FLAG-purified MRI in different-sized fractions separated by a sucrose gradient column.
Mbp, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/scanr+inverted+microscope+high+content+screening+station/Protein+A+Magnetic+Beads/pmc06083883-824-9-30
Average 97 stars, based on 1 article reviews
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Nikon laser scanning nikon axr inverted confocal microscope
(A) Western blot analyses of DDR proteins that co-immunoprecipitated with FLAG-HA-tagged MRI in WT and Ku70−/− abl pre-B cell nuclear extracts using anti-HA. (B) Schematic of sequential immunoprecipitations of MRI followed by Ku80 in cells expressing HA-MRI and FLAG-Ku80 (left). Western blot analyses of ATM, DNA-PKcs, Ku70, FLAG-Ku80, and HA-MRI from MRI−/− abl pre-B cell nuclear extract after first immunoprecipitation with anti-HA (Input HA IP) and following second immunoprecipitation with anti-FLAG or an IgG isotype control (right). (C) Western blot analyses of <t>purified</t> <t>recombinant</t> biotin-FLAG-ATM (bio-F-ATM) co-immunoprecipitated with 50 nM, 100 nM, or 200 nM of <t>MBP-tagged</t> human MRI, MRIΔN, and MRIΔC proteins. (D) Western blot analyses of DDR proteins that associated with FLAG-purified MRI in different-sized fractions separated by a sucrose gradient column.
Laser Scanning Nikon Axr Inverted Confocal Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/scanr+inverted+microscope+high+content+screening+station/NIS-Elements/ppr0903943-117-12-14
Average 99 stars, based on 1 article reviews
laser scanning nikon axr inverted confocal microscope - by Bioz Stars, 2026-09
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Nikon eclipse te2000 e inverted confocal laser scanning microscope
(A) Western blot analyses of DDR proteins that co-immunoprecipitated with FLAG-HA-tagged MRI in WT and Ku70−/− abl pre-B cell nuclear extracts using anti-HA. (B) Schematic of sequential immunoprecipitations of MRI followed by Ku80 in cells expressing HA-MRI and FLAG-Ku80 (left). Western blot analyses of ATM, DNA-PKcs, Ku70, FLAG-Ku80, and HA-MRI from MRI−/− abl pre-B cell nuclear extract after first immunoprecipitation with anti-HA (Input HA IP) and following second immunoprecipitation with anti-FLAG or an IgG isotype control (right). (C) Western blot analyses of <t>purified</t> <t>recombinant</t> biotin-FLAG-ATM (bio-F-ATM) co-immunoprecipitated with 50 nM, 100 nM, or 200 nM of <t>MBP-tagged</t> human MRI, MRIΔN, and MRIΔC proteins. (D) Western blot analyses of DDR proteins that associated with FLAG-purified MRI in different-sized fractions separated by a sucrose gradient column.
Eclipse Te2000 E Inverted Confocal Laser Scanning Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/scanr+inverted+microscope+high+content+screening+station/Objectives/pm25391492-250-7-6
Average 99 stars, based on 1 article reviews
eclipse te2000 e inverted confocal laser scanning microscope - by Bioz Stars, 2026-09
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Danaher Inc dmi8 microscope
(A) Western blot analyses of DDR proteins that co-immunoprecipitated with FLAG-HA-tagged MRI in WT and Ku70−/− abl pre-B cell nuclear extracts using anti-HA. (B) Schematic of sequential immunoprecipitations of MRI followed by Ku80 in cells expressing HA-MRI and FLAG-Ku80 (left). Western blot analyses of ATM, DNA-PKcs, Ku70, FLAG-Ku80, and HA-MRI from MRI−/− abl pre-B cell nuclear extract after first immunoprecipitation with anti-HA (Input HA IP) and following second immunoprecipitation with anti-FLAG or an IgG isotype control (right). (C) Western blot analyses of <t>purified</t> <t>recombinant</t> biotin-FLAG-ATM (bio-F-ATM) co-immunoprecipitated with 50 nM, 100 nM, or 200 nM of <t>MBP-tagged</t> human MRI, MRIΔN, and MRIΔC proteins. (D) Western blot analyses of DDR proteins that associated with FLAG-purified MRI in different-sized fractions separated by a sucrose gradient column.
Dmi8 Microscope, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/scanr+inverted+microscope+high+content+screening+station/DMi8+S+Inverted+Microscope+Solution/bio_rxiv__2025__08__26__672304-203-18-20
Average 99 stars, based on 1 article reviews
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Danaher Inc stellaris 5 confocal laser scanning inverted microscope
(A) Western blot analyses of DDR proteins that co-immunoprecipitated with FLAG-HA-tagged MRI in WT and Ku70−/− abl pre-B cell nuclear extracts using anti-HA. (B) Schematic of sequential immunoprecipitations of MRI followed by Ku80 in cells expressing HA-MRI and FLAG-Ku80 (left). Western blot analyses of ATM, DNA-PKcs, Ku70, FLAG-Ku80, and HA-MRI from MRI−/− abl pre-B cell nuclear extract after first immunoprecipitation with anti-HA (Input HA IP) and following second immunoprecipitation with anti-FLAG or an IgG isotype control (right). (C) Western blot analyses of <t>purified</t> <t>recombinant</t> biotin-FLAG-ATM (bio-F-ATM) co-immunoprecipitated with 50 nM, 100 nM, or 200 nM of <t>MBP-tagged</t> human MRI, MRIΔN, and MRIΔC proteins. (D) Western blot analyses of DDR proteins that associated with FLAG-purified MRI in different-sized fractions separated by a sucrose gradient column.
Stellaris 5 Confocal Laser Scanning Inverted Microscope, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/scanr+inverted+microscope+high+content+screening+station/STELLARIS+5+Confocal+Microscope+Platforms/bio_rxiv__64898__2025__12__19__695615-256-17-16
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98
Danaher Inc leica inverted microscope
(A) Western blot analyses of DDR proteins that co-immunoprecipitated with FLAG-HA-tagged MRI in WT and Ku70−/− abl pre-B cell nuclear extracts using anti-HA. (B) Schematic of sequential immunoprecipitations of MRI followed by Ku80 in cells expressing HA-MRI and FLAG-Ku80 (left). Western blot analyses of ATM, DNA-PKcs, Ku70, FLAG-Ku80, and HA-MRI from MRI−/− abl pre-B cell nuclear extract after first immunoprecipitation with anti-HA (Input HA IP) and following second immunoprecipitation with anti-FLAG or an IgG isotype control (right). (C) Western blot analyses of <t>purified</t> <t>recombinant</t> biotin-FLAG-ATM (bio-F-ATM) co-immunoprecipitated with 50 nM, 100 nM, or 200 nM of <t>MBP-tagged</t> human MRI, MRIΔN, and MRIΔC proteins. (D) Western blot analyses of DDR proteins that associated with FLAG-purified MRI in different-sized fractions separated by a sucrose gradient column.
Leica Inverted Microscope, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/scanr+inverted+microscope+high+content+screening+station/DMi1+Inverted+Microscope/pm36233314-444-11-11
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Image Search Results


A Fluorescent images of tumor cells treated with TMTP1-DKK were examined with Confocal laser scanning microscopy. (a) PC-3M-1E8 cells (b) PC-3M-2B4 cells (c) MKN-45sci cells (d) NIH/3T3 cells. FITC-TMTP1-DKK (green) and control peptide were examined in xenograft tumors including PC-3M-1E8 (e)TMTP1-DKK, (f)svTMTP1-DKK, MKN-45sci (g) TMTP1-DKK, (h) svTMTP1-DKK. Nuclei were co-stained with DAPI (blue). B Fluorescent images of nomal cells (normal mammary epithelial cell MCF-10A, normal liver cell LO2 and HEK293 cells) treated with TMTP1-DKK were examined with Confocal laser scanning microscopy. The morphological change of nomal cells was visualized using inverted microscope.

Journal: PLoS ONE

Article Title: Anti-Tumor Effects of the Peptide TMTP1-GG- D (KLAKLAK) 2 on Highly Metastatic Cancers

doi: 10.1371/journal.pone.0042685

Figure Lengend Snippet: A Fluorescent images of tumor cells treated with TMTP1-DKK were examined with Confocal laser scanning microscopy. (a) PC-3M-1E8 cells (b) PC-3M-2B4 cells (c) MKN-45sci cells (d) NIH/3T3 cells. FITC-TMTP1-DKK (green) and control peptide were examined in xenograft tumors including PC-3M-1E8 (e)TMTP1-DKK, (f)svTMTP1-DKK, MKN-45sci (g) TMTP1-DKK, (h) svTMTP1-DKK. Nuclei were co-stained with DAPI (blue). B Fluorescent images of nomal cells (normal mammary epithelial cell MCF-10A, normal liver cell LO2 and HEK293 cells) treated with TMTP1-DKK were examined with Confocal laser scanning microscopy. The morphological change of nomal cells was visualized using inverted microscope.

Article Snippet: The human gastric cancer cell lineMKN-45sci, the murine fibroblast NIH/3T3 cells, normal mammary epithelial cell MCF-10A, normal liver cell LO2 and HEK293 cells were obtained from the American Type Culture Collection (Manassas, VA, USA).

Techniques: Confocal Laser Scanning Microscopy, Control, Staining, Inverted Microscopy

(A) Western blot analyses of DDR proteins that co-immunoprecipitated with FLAG-HA-tagged MRI in WT and Ku70−/− abl pre-B cell nuclear extracts using anti-HA. (B) Schematic of sequential immunoprecipitations of MRI followed by Ku80 in cells expressing HA-MRI and FLAG-Ku80 (left). Western blot analyses of ATM, DNA-PKcs, Ku70, FLAG-Ku80, and HA-MRI from MRI−/− abl pre-B cell nuclear extract after first immunoprecipitation with anti-HA (Input HA IP) and following second immunoprecipitation with anti-FLAG or an IgG isotype control (right). (C) Western blot analyses of purified recombinant biotin-FLAG-ATM (bio-F-ATM) co-immunoprecipitated with 50 nM, 100 nM, or 200 nM of MBP-tagged human MRI, MRIΔN, and MRIΔC proteins. (D) Western blot analyses of DDR proteins that associated with FLAG-purified MRI in different-sized fractions separated by a sucrose gradient column.

Journal: Molecular cell

Article Title: MRI is a DNA Damage Response Adaptor during Classical Non-Homologous End Joining

doi: 10.1016/j.molcel.2018.06.018

Figure Lengend Snippet: (A) Western blot analyses of DDR proteins that co-immunoprecipitated with FLAG-HA-tagged MRI in WT and Ku70−/− abl pre-B cell nuclear extracts using anti-HA. (B) Schematic of sequential immunoprecipitations of MRI followed by Ku80 in cells expressing HA-MRI and FLAG-Ku80 (left). Western blot analyses of ATM, DNA-PKcs, Ku70, FLAG-Ku80, and HA-MRI from MRI−/− abl pre-B cell nuclear extract after first immunoprecipitation with anti-HA (Input HA IP) and following second immunoprecipitation with anti-FLAG or an IgG isotype control (right). (C) Western blot analyses of purified recombinant biotin-FLAG-ATM (bio-F-ATM) co-immunoprecipitated with 50 nM, 100 nM, or 200 nM of MBP-tagged human MRI, MRIΔN, and MRIΔC proteins. (D) Western blot analyses of DDR proteins that associated with FLAG-purified MRI in different-sized fractions separated by a sucrose gradient column.

Article Snippet: 40 nM recombinant biotin-FLAG-tagged human ATM was incubated with MBP-tagged human MRI, MRI ΔN , or MRI ΔC (50, 100, or 200 nM) and 100 ng bovine serum albumin (BSA, New England Biolabs) in A buffer (25 mM Tris-HCl pH 8.0, 100 mM NaCl, 10% v/v glycerol) at room temperature for 15 minutes in a final volume of 30 μL.

Techniques: Western Blot, Immunoprecipitation, Expressing, Purification, Recombinant

KEY RESOURCES TABLE

Journal: Molecular cell

Article Title: MRI is a DNA Damage Response Adaptor during Classical Non-Homologous End Joining

doi: 10.1016/j.molcel.2018.06.018

Figure Lengend Snippet: KEY RESOURCES TABLE

Article Snippet: 40 nM recombinant biotin-FLAG-tagged human ATM was incubated with MBP-tagged human MRI, MRI ΔN , or MRI ΔC (50, 100, or 200 nM) and 100 ng bovine serum albumin (BSA, New England Biolabs) in A buffer (25 mM Tris-HCl pH 8.0, 100 mM NaCl, 10% v/v glycerol) at room temperature for 15 minutes in a final volume of 30 μL.

Techniques: Blocking Assay, Recombinant, Cell Isolation, Magnetic Beads, Mass Spectrometry, Magnetic Resonance Imaging, Sequencing, Plasmid Preparation, Software, High Content Screening, Flow Cytometry, Inverted Microscopy, Laser-Scanning Microscopy, Spectrophotometry, Irradiation