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Santa Cruz Biotechnology dapi
Dapi, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1459 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dapi+staining+solution+c1002/DAPI/pm38969190-76-38-16
Average 96 stars, based on 1459 article reviews
dapi - by Bioz Stars, 2026-11
96/100 stars

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Related Articles

Staining:

Article Title: Exposure of Human Corneal Epithelial Cells to Microplastic Particles Induces a Phase-Specific Cytokine Response.
Article Snippet: 37 Microplastics have been identified in ophthalmic therapeutics and linked to dry eye 38 disease and meibomian gland dysfunction.. Inflammation is hypothesised to drive 39 ocular surface damage.. This in-vitro study investigates how varying concentrations of 40 microplastics affect corneal cell viability and cytokine expression.

Article Title: CD200 + fibroblasts prime the immunoregulatory function of granulocytic myeloid-derived suppressor cells in inflammatory arthritis.
Article Snippet: .. Secondary antibodies were stained for 1 h at room temperature followed by incubation with DAPI nuclear staining (1:1000, Cat# sc-3598, Santa Cruz). .. The following antibodies were used in human tissues: anti-CD33 (Polyclonal, 1:100, Cat# bs-2042R, Bioss), Nature Communications | (2026) 17:10746 12 anti-HLA-DR (LN3, 1:100, Cat# LS-B8114, LSBio), anti-CD20 (H1, 1:500, Cat# 555677, BD Biosciences), anti-CD56 (123A8, 1:1000, Cat# NBP244713, Novus), anti-CD11c (Polyclonal, 1:300, Cat# orb13554, Biorbyt), anti-CD3 (PS1, 1:50, Cat# ab699, Abcam), anti-CD14 (4B4F12, 1:100, Cat# ab182032, Abcam), anti-CD16 (2Q1240, 1:50, Cat# sc-70548, Santa Cruz), anti-CD123 (6H6, 1:100, Cat# 306002, BioLegend), anti-CD274/ PD-L1 (E1L3N, 1:100, Cat# 85164SF, Cell Signaling), anti-CD200 (Polyclonal, 1:100, Cat#AF2724, R&DSystems), anti-Podoplanin (Polyclonal, 1:100, Cat# AF3670, R&D Systems).

Article Title: Macrophage-derived IL-6 reprograms lipid metabolism to promote colorectal cancer development through USP14-mediated FASN deubiquitination
Article Snippet: For immunohistochemistry, the slices were incubated with antibodies against IL-6 (Cat#AF-206-NA, R&D Systems, Minneapolis, Minnesota, USA), p-STAT3 (Cell Signaling Technology, Danvers, Massachusetts, USA), USP14 (Proteintech, Wuhan, Hubei, China) and FASN (Cat#10624-2-AP, Proteintech) and then treated with an HRP-labeled secondary antibody (Proteintech). .. After the final round of staining, DAPI (Cat#sc-3598, Santa Cruz Biotechnology, Texas, USA) solution was added. .. Photomicrographs were obtained via a light microscope (Leica, Germany).

Article Title: Glycine receptors in circulating white blood cells regulated by neuroinflammation
Article Snippet: After incubation, the slides were washed three times with PBS for 5 minutes each, then incubated with appropriate secondary antibodies, i.e., Alexa Fluor 488 (1:200) and/or 594 (1:200) (Thermo-Fisher Scientific) for 1 hour at room temperature. .. A DAPI mounting agent (# AB104139 , Santa Cruz Biotechnology) was used for nuclear staining and mounting. ..

Fluorescence:

Article Title: Exposure of Human Corneal Epithelial Cells to Microplastic Particles Induces a Phase-Specific Cytokine Response.
Article Snippet: 37 Microplastics have been identified in ophthalmic therapeutics and linked to dry eye 38 disease and meibomian gland dysfunction.. Inflammation is hypothesised to drive 39 ocular surface damage.. This in-vitro study investigates how varying concentrations of 40 microplastics affect corneal cell viability and cytokine expression.

Microscopy:

Article Title: Exposure of Human Corneal Epithelial Cells to Microplastic Particles Induces a Phase-Specific Cytokine Response.
Article Snippet: 37 Microplastics have been identified in ophthalmic therapeutics and linked to dry eye 38 disease and meibomian gland dysfunction.. Inflammation is hypothesised to drive 39 ocular surface damage.. This in-vitro study investigates how varying concentrations of 40 microplastics affect corneal cell viability and cytokine expression.

Incubation:

Article Title: CD200 + fibroblasts prime the immunoregulatory function of granulocytic myeloid-derived suppressor cells in inflammatory arthritis.
Article Snippet: .. Secondary antibodies were stained for 1 h at room temperature followed by incubation with DAPI nuclear staining (1:1000, Cat# sc-3598, Santa Cruz). .. The following antibodies were used in human tissues: anti-CD33 (Polyclonal, 1:100, Cat# bs-2042R, Bioss), Nature Communications | (2026) 17:10746 12 anti-HLA-DR (LN3, 1:100, Cat# LS-B8114, LSBio), anti-CD20 (H1, 1:500, Cat# 555677, BD Biosciences), anti-CD56 (123A8, 1:1000, Cat# NBP244713, Novus), anti-CD11c (Polyclonal, 1:300, Cat# orb13554, Biorbyt), anti-CD3 (PS1, 1:50, Cat# ab699, Abcam), anti-CD14 (4B4F12, 1:100, Cat# ab182032, Abcam), anti-CD16 (2Q1240, 1:50, Cat# sc-70548, Santa Cruz), anti-CD123 (6H6, 1:100, Cat# 306002, BioLegend), anti-CD274/ PD-L1 (E1L3N, 1:100, Cat# 85164SF, Cell Signaling), anti-CD200 (Polyclonal, 1:100, Cat#AF2724, R&DSystems), anti-Podoplanin (Polyclonal, 1:100, Cat# AF3670, R&D Systems).

Article Title: Submedius thalamic inputs shape the presynaptic architecture of layer 5 orbitofrontal cortex in mice
Article Snippet: For quantitative analysis of trans-synaptic tracing, 40-μm coronal sections of the whole brain were collected using cryostat (model #CM1860; Leica). .. Free-floating slices were incubated at room temperature with gentle agitation as follows: 2 h in blocking solution (5% heat-inactivated goat serum, 0.4% Triton X-100 in PBS); overnight in primary antibody diluted 1:1000 in blocking solution (mouse anti-GFP, GFP-1010, Aves Labs; or anti-RFP, 5f8, Chromotek); 2–3 h in secondary antibody diluted 1:500 (donkey anti-chicken-IgY Alexa488 or goat anti-rat IgG Cy3, Jackson ImmunoResearch); and 15 min in 2.5 μg/mL of DAPI (Santa Cruz, Cat #sc-3598) in PBS. .. Mice were anesthetized with 65 mg/kg ketamine (Daiichi-Sankyo) and 13 mg/kg xylazine (Sigma-Aldrich) via intraperitoneal injection and head-fixed in stereotaxic equipment (Narishige).

Article Title: Donor-intrinsic regenerative potential outweighs histocompatibility in iPSC-derived skeletal muscle engraftment in nonhuman primates.
Article Snippet: Cultured cells were washed with PBS and fixed with 4% paraformaldehyde (Millipore Sigma) for 15 min. .. Cells were then permeabilized with 0.3% Triton X-100 (Millipore Sigma) in PBS for 15 min at room temperature, blocked with 3% Bovine Serum Albumin (BSA) in PBS for 45 min, and incubated with primary antibodies overnight at 4 ◦ C. Following washing, cells were incubated with fluorophore-conjugated secondary antibodies containing DAPI (Santa Cruz, Dallas, TX, USA) for 1 h at room temperature. .. Mouse muscle cryosections were fixed with 4% paraformaldehyde, permeabilized with 0.3% Triton X-100 in PBS, blocked with 3% BSA, and incubated with primary antibodies overnight at 4 ◦ C. Sections were subsequently incubated with secondary antibodies and mounted using ProLong Gold Antifade Mountant with DAPI (Thermo Fisher Scientific).

Gentle:

Article Title: Submedius thalamic inputs shape the presynaptic architecture of layer 5 orbitofrontal cortex in mice
Article Snippet: For quantitative analysis of trans-synaptic tracing, 40-μm coronal sections of the whole brain were collected using cryostat (model #CM1860; Leica). .. Free-floating slices were incubated at room temperature with gentle agitation as follows: 2 h in blocking solution (5% heat-inactivated goat serum, 0.4% Triton X-100 in PBS); overnight in primary antibody diluted 1:1000 in blocking solution (mouse anti-GFP, GFP-1010, Aves Labs; or anti-RFP, 5f8, Chromotek); 2–3 h in secondary antibody diluted 1:500 (donkey anti-chicken-IgY Alexa488 or goat anti-rat IgG Cy3, Jackson ImmunoResearch); and 15 min in 2.5 μg/mL of DAPI (Santa Cruz, Cat #sc-3598) in PBS. .. Mice were anesthetized with 65 mg/kg ketamine (Daiichi-Sankyo) and 13 mg/kg xylazine (Sigma-Aldrich) via intraperitoneal injection and head-fixed in stereotaxic equipment (Narishige).

Blocking Assay:

Article Title: Submedius thalamic inputs shape the presynaptic architecture of layer 5 orbitofrontal cortex in mice
Article Snippet: For quantitative analysis of trans-synaptic tracing, 40-μm coronal sections of the whole brain were collected using cryostat (model #CM1860; Leica). .. Free-floating slices were incubated at room temperature with gentle agitation as follows: 2 h in blocking solution (5% heat-inactivated goat serum, 0.4% Triton X-100 in PBS); overnight in primary antibody diluted 1:1000 in blocking solution (mouse anti-GFP, GFP-1010, Aves Labs; or anti-RFP, 5f8, Chromotek); 2–3 h in secondary antibody diluted 1:500 (donkey anti-chicken-IgY Alexa488 or goat anti-rat IgG Cy3, Jackson ImmunoResearch); and 15 min in 2.5 μg/mL of DAPI (Santa Cruz, Cat #sc-3598) in PBS. .. Mice were anesthetized with 65 mg/kg ketamine (Daiichi-Sankyo) and 13 mg/kg xylazine (Sigma-Aldrich) via intraperitoneal injection and head-fixed in stereotaxic equipment (Narishige).

FACS:

Article Title: Combination therapy with targeted 4-1BB (CD137) agonists/anti-FAP binding domain and anti-CEA/anti-CD3 bispecific antibody
Article Snippet: Cells were surface-stained with fluorescent dye-conjugated antibodies anti-human CD4 (clone RPA-T4, BioLegend, Cat.-No. 300532), CD8 (clone RPa-T8, BioLegend, Cat.-No. 3010441), CD62L (clone DREG-56, BioLegend, Cat.-No. 304834), CD127 (clone 019D5, BioLegend, Cat.-No. A019D5), CD134 (clone Ber-ACT35, BioLegend, Cat.-No. 350008), CD137 (clone 4B4-1, BioLegend, Cat.-No. 309814), GITR (clone 621, BioLegend, Cat.-No. 3311608) and CD25 (clone M-A251, BioLegend, Cat.-No. 356112) for 20 min at 4° C. in FACS buffer. .. Then, they were washed once with FACS buffer before being resuspended in 85 μL/well FACS buffer containing containing 0.2 μg/mL DAPI (Santa Cruz Biotec, Cat. No. Sc-3598) before they were acquired the same day using 5-laser LSR-Fortessa (BD Bioscience with DIVA software). ..

Software:

Article Title: Combination therapy with targeted 4-1BB (CD137) agonists/anti-FAP binding domain and anti-CEA/anti-CD3 bispecific antibody
Article Snippet: Cells were surface-stained with fluorescent dye-conjugated antibodies anti-human CD4 (clone RPA-T4, BioLegend, Cat.-No. 300532), CD8 (clone RPa-T8, BioLegend, Cat.-No. 3010441), CD62L (clone DREG-56, BioLegend, Cat.-No. 304834), CD127 (clone 019D5, BioLegend, Cat.-No. A019D5), CD134 (clone Ber-ACT35, BioLegend, Cat.-No. 350008), CD137 (clone 4B4-1, BioLegend, Cat.-No. 309814), GITR (clone 621, BioLegend, Cat.-No. 3311608) and CD25 (clone M-A251, BioLegend, Cat.-No. 356112) for 20 min at 4° C. in FACS buffer. .. Then, they were washed once with FACS buffer before being resuspended in 85 μL/well FACS buffer containing containing 0.2 μg/mL DAPI (Santa Cruz Biotec, Cat. No. Sc-3598) before they were acquired the same day using 5-laser LSR-Fortessa (BD Bioscience with DIVA software). ..



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Rab1a exaggerated extracellular matrix degradation and apoptosis in mice. A) Protein deposition of Rab1a, MMP13, ADAMTS5, and Aggrecan in articular cartilage with transfection by Rab1a AAV or control AAV were exhibited via immunohistochemical analysis, Scale bar, 20 μm. B) Protein deposition of Rab1a, MMP13, ADAMTS5, and Aggrecan in articular cartilage with transfection by Ad-Rab1a or Ad-NC were detected using immunohistochemical analysis, scale bar, 20 μm. C) Quantification of A. n = 6. D) Quantification of B. n = 6. E, F) TUNEL staining of chondrocytes in hyaline cartilage (HC) and calcified cartilage (CC) of each group. Blue fluorescence <t>(DAPI)</t> represented the nucleus, and green fluorescence (fluorescein-dUTP) represented TUNEL-positive cells. Scale bar, 25 μm. G, H) Quantification of TUNEL-positive chondrocytes relative to total chondrocytes was shown. n = 6. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. TUNEL: TdT-mediated dUTP Nick-End Labeling.
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Image Search Results


Rab1a exaggerated extracellular matrix degradation and apoptosis in mice. A) Protein deposition of Rab1a, MMP13, ADAMTS5, and Aggrecan in articular cartilage with transfection by Rab1a AAV or control AAV were exhibited via immunohistochemical analysis, Scale bar, 20 μm. B) Protein deposition of Rab1a, MMP13, ADAMTS5, and Aggrecan in articular cartilage with transfection by Ad-Rab1a or Ad-NC were detected using immunohistochemical analysis, scale bar, 20 μm. C) Quantification of A. n = 6. D) Quantification of B. n = 6. E, F) TUNEL staining of chondrocytes in hyaline cartilage (HC) and calcified cartilage (CC) of each group. Blue fluorescence (DAPI) represented the nucleus, and green fluorescence (fluorescein-dUTP) represented TUNEL-positive cells. Scale bar, 25 μm. G, H) Quantification of TUNEL-positive chondrocytes relative to total chondrocytes was shown. n = 6. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. TUNEL: TdT-mediated dUTP Nick-End Labeling.

Journal: Journal of Advanced Research

Article Title: Increased Rab1a accelerates osteoarthritis by inhibiting autophagy via activation of the mTORC1-S6K pathway

doi: 10.1016/j.jare.2024.11.009

Figure Lengend Snippet: Rab1a exaggerated extracellular matrix degradation and apoptosis in mice. A) Protein deposition of Rab1a, MMP13, ADAMTS5, and Aggrecan in articular cartilage with transfection by Rab1a AAV or control AAV were exhibited via immunohistochemical analysis, Scale bar, 20 μm. B) Protein deposition of Rab1a, MMP13, ADAMTS5, and Aggrecan in articular cartilage with transfection by Ad-Rab1a or Ad-NC were detected using immunohistochemical analysis, scale bar, 20 μm. C) Quantification of A. n = 6. D) Quantification of B. n = 6. E, F) TUNEL staining of chondrocytes in hyaline cartilage (HC) and calcified cartilage (CC) of each group. Blue fluorescence (DAPI) represented the nucleus, and green fluorescence (fluorescein-dUTP) represented TUNEL-positive cells. Scale bar, 25 μm. G, H) Quantification of TUNEL-positive chondrocytes relative to total chondrocytes was shown. n = 6. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. TUNEL: TdT-mediated dUTP Nick-End Labeling.

Article Snippet: Subsequently, The TUNEL reaction mixture was applied at room temperature for 1 h. This was followed by coloring the nuclei with DAPI Staining Solution(Beyotime, China).

Techniques: Transfection, Control, Immunohistochemical staining, TUNEL Assay, Staining, Fluorescence, End Labeling