ultracruz hardset mounting medium plus dapi Search Results


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Santa Cruz Biotechnology ultracruztm mounting medium
Ultracruztm Mounting Medium, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Santa Cruz Biotechnology ultracruz hardset mounting medium plus dapi
Amiloride promoted ErbB3 translocation from the nucleus to the cytoplasm and the plasma membrane in HSPC cells ( A ) Hormone-sensitive LNCaP cells were treated with varying concentrations of amiloride for 72 h before being lysed, fractionated and analyzed by immunoblot. ( B ) Immunofluorescence microscopy (IF) in LNCaP cells treated with DMSO or 75 µM or and probed with IF specific C-terminal ErbB3 antibodies or ( C ) 10µM or 25µM amiloride and probed with IF specific N-terminal ErbB3 antibodies for 72 h (scale bars = 30 μm). Note that vehicle treated LNCaP cells expressed nuclear ErbB3 (red) whereas amiloride-treated cells had significantly decreased ErbB3 expression in the nucleus (hollowed out). Location of nuclei are identified by blue <t>DAPI</t> staining. Plasma membrane localization of ErbB3 at cell-cell junction was also noted in amiloride-treated but not in vehicle treated cells. Note that both N- and C-terminal ErbB3 antibodies demonstrate lighter nuclear staining in amiloride-treated cells. ( D ) Cells were subjected to viability assays using the stated concentrations of amiloride. p-values are calculated with respect to DMSO
Ultracruz Hardset Mounting Medium Plus Dapi, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Santa Cruz Biotechnology ultracruz mounting media
Amiloride promoted ErbB3 translocation from the nucleus to the cytoplasm and the plasma membrane in HSPC cells ( A ) Hormone-sensitive LNCaP cells were treated with varying concentrations of amiloride for 72 h before being lysed, fractionated and analyzed by immunoblot. ( B ) Immunofluorescence microscopy (IF) in LNCaP cells treated with DMSO or 75 µM or and probed with IF specific C-terminal ErbB3 antibodies or ( C ) 10µM or 25µM amiloride and probed with IF specific N-terminal ErbB3 antibodies for 72 h (scale bars = 30 μm). Note that vehicle treated LNCaP cells expressed nuclear ErbB3 (red) whereas amiloride-treated cells had significantly decreased ErbB3 expression in the nucleus (hollowed out). Location of nuclei are identified by blue <t>DAPI</t> staining. Plasma membrane localization of ErbB3 at cell-cell junction was also noted in amiloride-treated but not in vehicle treated cells. Note that both N- and C-terminal ErbB3 antibodies demonstrate lighter nuclear staining in amiloride-treated cells. ( D ) Cells were subjected to viability assays using the stated concentrations of amiloride. p-values are calculated with respect to DMSO
Ultracruz Mounting Media, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Santa Cruz Biotechnology 4 6 diamidino 2phenylindole dapi
Amiloride promoted ErbB3 translocation from the nucleus to the cytoplasm and the plasma membrane in HSPC cells ( A ) Hormone-sensitive LNCaP cells were treated with varying concentrations of amiloride for 72 h before being lysed, fractionated and analyzed by immunoblot. ( B ) Immunofluorescence microscopy (IF) in LNCaP cells treated with DMSO or 75 µM or and probed with IF specific C-terminal ErbB3 antibodies or ( C ) 10µM or 25µM amiloride and probed with IF specific N-terminal ErbB3 antibodies for 72 h (scale bars = 30 μm). Note that vehicle treated LNCaP cells expressed nuclear ErbB3 (red) whereas amiloride-treated cells had significantly decreased ErbB3 expression in the nucleus (hollowed out). Location of nuclei are identified by blue <t>DAPI</t> staining. Plasma membrane localization of ErbB3 at cell-cell junction was also noted in amiloride-treated but not in vehicle treated cells. Note that both N- and C-terminal ErbB3 antibodies demonstrate lighter nuclear staining in amiloride-treated cells. ( D ) Cells were subjected to viability assays using the stated concentrations of amiloride. p-values are calculated with respect to DMSO
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Santa Cruz Biotechnology ultracruz aqueous mounting medium with dapi
Immunofluorescence image showing a cross-section of the retina after CS/HA-EPOβ administration: ( a ) OD from group A; ( b ) OS from group A (control); ( c ) OD from group F; ( d ) OS from group F (control). Green and blue channels were merged, and green tissue auto-fluorescence is visible in ( b , d ). Red arrows indicate EPOβ and cell nuclei are blue <t>(DAPI)</t> (40 × ). GCL, ganglion cell layer; INL, inner nuclear layer; ONL, outer nuclear layer.
Ultracruz Aqueous Mounting Medium With Dapi, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Vector Laboratories dna counterstaining
Immunofluorescence image showing a cross-section of the retina after CS/HA-EPOβ administration: ( a ) OD from group A; ( b ) OS from group A (control); ( c ) OD from group F; ( d ) OS from group F (control). Green and blue channels were merged, and green tissue auto-fluorescence is visible in ( b , d ). Red arrows indicate EPOβ and cell nuclei are blue <t>(DAPI)</t> (40 × ). GCL, ganglion cell layer; INL, inner nuclear layer; ONL, outer nuclear layer.
Dna Counterstaining, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Santa Cruz Biotechnology ultracruz dapi mounting media
Immunofluorescence image showing a cross-section of the retina after CS/HA-EPOβ administration: ( a ) OD from group A; ( b ) OS from group A (control); ( c ) OD from group F; ( d ) OS from group F (control). Green and blue channels were merged, and green tissue auto-fluorescence is visible in ( b , d ). Red arrows indicate EPOβ and cell nuclei are blue <t>(DAPI)</t> (40 × ). GCL, ganglion cell layer; INL, inner nuclear layer; ONL, outer nuclear layer.
Ultracruz Dapi Mounting Media, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Amiloride promoted ErbB3 translocation from the nucleus to the cytoplasm and the plasma membrane in HSPC cells ( A ) Hormone-sensitive LNCaP cells were treated with varying concentrations of amiloride for 72 h before being lysed, fractionated and analyzed by immunoblot. ( B ) Immunofluorescence microscopy (IF) in LNCaP cells treated with DMSO or 75 µM or and probed with IF specific C-terminal ErbB3 antibodies or ( C ) 10µM or 25µM amiloride and probed with IF specific N-terminal ErbB3 antibodies for 72 h (scale bars = 30 μm). Note that vehicle treated LNCaP cells expressed nuclear ErbB3 (red) whereas amiloride-treated cells had significantly decreased ErbB3 expression in the nucleus (hollowed out). Location of nuclei are identified by blue DAPI staining. Plasma membrane localization of ErbB3 at cell-cell junction was also noted in amiloride-treated but not in vehicle treated cells. Note that both N- and C-terminal ErbB3 antibodies demonstrate lighter nuclear staining in amiloride-treated cells. ( D ) Cells were subjected to viability assays using the stated concentrations of amiloride. p-values are calculated with respect to DMSO

Journal: Cellular and Molecular Life Sciences: CMLS

Article Title: Amiloride sensitizes prostate cancer cells to the reversible tyrosine kinase inhibitor lapatinib by modulating Erbb3 subcellular localization

doi: 10.1007/s00018-024-05540-5

Figure Lengend Snippet: Amiloride promoted ErbB3 translocation from the nucleus to the cytoplasm and the plasma membrane in HSPC cells ( A ) Hormone-sensitive LNCaP cells were treated with varying concentrations of amiloride for 72 h before being lysed, fractionated and analyzed by immunoblot. ( B ) Immunofluorescence microscopy (IF) in LNCaP cells treated with DMSO or 75 µM or and probed with IF specific C-terminal ErbB3 antibodies or ( C ) 10µM or 25µM amiloride and probed with IF specific N-terminal ErbB3 antibodies for 72 h (scale bars = 30 μm). Note that vehicle treated LNCaP cells expressed nuclear ErbB3 (red) whereas amiloride-treated cells had significantly decreased ErbB3 expression in the nucleus (hollowed out). Location of nuclei are identified by blue DAPI staining. Plasma membrane localization of ErbB3 at cell-cell junction was also noted in amiloride-treated but not in vehicle treated cells. Note that both N- and C-terminal ErbB3 antibodies demonstrate lighter nuclear staining in amiloride-treated cells. ( D ) Cells were subjected to viability assays using the stated concentrations of amiloride. p-values are calculated with respect to DMSO

Article Snippet: After washing thrice with cold PBST, coverslips were inverted and mounted onto uncharged glass slides with UltraCruz Hardset Mounting Medium plus DAPI (SantaCruz BioTech, Dallas, TX).

Techniques: Translocation Assay, Clinical Proteomics, Membrane, Western Blot, Immunofluorescence, Microscopy, Expressing, Staining

Immunofluorescence image showing a cross-section of the retina after CS/HA-EPOβ administration: ( a ) OD from group A; ( b ) OS from group A (control); ( c ) OD from group F; ( d ) OS from group F (control). Green and blue channels were merged, and green tissue auto-fluorescence is visible in ( b , d ). Red arrows indicate EPOβ and cell nuclei are blue (DAPI) (40 × ). GCL, ganglion cell layer; INL, inner nuclear layer; ONL, outer nuclear layer.

Journal: Marine Drugs

Article Title: Chitosan and Hyaluronic Acid Nanoparticles as Vehicles of Epoetin Beta for Subconjunctival Ocular Delivery

doi: 10.3390/md20020151

Figure Lengend Snippet: Immunofluorescence image showing a cross-section of the retina after CS/HA-EPOβ administration: ( a ) OD from group A; ( b ) OS from group A (control); ( c ) OD from group F; ( d ) OS from group F (control). Green and blue channels were merged, and green tissue auto-fluorescence is visible in ( b , d ). Red arrows indicate EPOβ and cell nuclei are blue (DAPI) (40 × ). GCL, ganglion cell layer; INL, inner nuclear layer; ONL, outer nuclear layer.

Article Snippet: The mounting medium used was UltraCruz ® Aqueous Mounting Medium with DAPI (sc-2494; Santa Cruz Biotechnology, Dallas, TX, USA).

Techniques: Immunofluorescence, Control, Fluorescence