progenitor cells Search Results


94
ATCC dopaminergic neuron differentiation kit
Dopaminergic Neuron Differentiation Kit, supplied by ATCC, 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/progenitor+cells/pmc10208675-181-8-25?v=ATCC
Average 94 stars, based on 1 article reviews
dopaminergic neuron differentiation kit - by Bioz Stars, 2026-08
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91
Celprogen Inc neural progenitor stem cells
Neural Progenitor Stem Cells, supplied by Celprogen Inc, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/progenitor+cells/pmc13067427-80-13-20?v=Celprogen+Inc
Average 91 stars, based on 1 article reviews
neural progenitor stem cells - by Bioz Stars, 2026-08
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94
MedChemExpress cd34 cells
Fig. 2 O‑GlcNAcylation weakens FTO expression. (A) Volcano diagram representing FTO expression after OSMI-1 treatment in KG1a cells; p-val ue < 0.05,|Fold change| > 1.5. (B) The correlation between O-GlcNAc levels and the survival of AML patients was explored using upper quartile analysis through the Kaplan-Meier Plotter. (C) The association between O-GlcNAc and FTO in a cohort of 14 MDS/AML patients by ELISA. (D) Western blot detec tion of FTO level in cKit + cells of the bone marrow from MLL-AF9-induced leukemia mice. (E) FTO level in primary <t>CD34</t> + cells from MDS/AML patients after 20 µM DMSO and 20 µg/mL OSMI-1 treatment. (F-G) FTO level in KG1a and SKM1 cells after TMG and OSMI-1 treatment
Cd34 Cells, supplied by MedChemExpress, 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/progenitor+cells/pm39849461-45-0-12?v=MedChemExpress
Average 94 stars, based on 1 article reviews
cd34 cells - by Bioz Stars, 2026-08
94/100 stars
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93
ATCC neural progenitor cells
Human Neural <t>Progenitor</t> Cells (NPCs) display increased neurite outgrowth when cultured with exosomes and CM from MCF-7 Snail cells compared to MCF-7 Neo. MCF-7 Neo or MCF-7 Snail was cultured in exosome-depleted medium (Exo-D medium) for 3 days, and conditioned medium (CM) was collected, or exosomes were isolated from the CM. These were subsequently cultured with NPCs for 2 days. (A) Images of NPC after incubation in NPC regular medium, Exo-D medium, exosomes or CM with or without Talin1 inhibitor mH4 were captured with a Nikon Eclipse TE2000-S Inverted Fluorescence Microscope. (B) The percentage of NPCs with neurite outgrowth and average neuron length was measured utilizing Image J Fiji Just software in NPCs cultured with NPC medium, Exo-D medium, and Exo-D medium plus NGF-beta as a positive control. The percentage of NPCs with neurite outgrowth and average neuron length of NPCs cultured with (C) exosomes isolated from MCF7-Neo and MCF7-Snail CM or (D) CM from MCF7-Neo and MCF7-Snail was analyzed using ImageJ Fiji Just software. Statistical analyses were done using GraphPad Prism software (one-way ANOVA, Šídák's multiple comparisons test, ****p< 0.0001, ***p< 0.001, **p < 0.01, *p < 0.05). Bars represent the SD of the mean. Results are representative of 3 experiments performed independently.
Neural Progenitor Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/progenitor+cells/pmc12825424-54-0-7?v=ATCC
Average 93 stars, based on 1 article reviews
neural progenitor cells - by Bioz Stars, 2026-08
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93
R&D Systems human mouse rat neural progenitor cell marker antibody panel
Human Neural <t>Progenitor</t> Cells (NPCs) display increased neurite outgrowth when cultured with exosomes and CM from MCF-7 Snail cells compared to MCF-7 Neo. MCF-7 Neo or MCF-7 Snail was cultured in exosome-depleted medium (Exo-D medium) for 3 days, and conditioned medium (CM) was collected, or exosomes were isolated from the CM. These were subsequently cultured with NPCs for 2 days. (A) Images of NPC after incubation in NPC regular medium, Exo-D medium, exosomes or CM with or without Talin1 inhibitor mH4 were captured with a Nikon Eclipse TE2000-S Inverted Fluorescence Microscope. (B) The percentage of NPCs with neurite outgrowth and average neuron length was measured utilizing Image J Fiji Just software in NPCs cultured with NPC medium, Exo-D medium, and Exo-D medium plus NGF-beta as a positive control. The percentage of NPCs with neurite outgrowth and average neuron length of NPCs cultured with (C) exosomes isolated from MCF7-Neo and MCF7-Snail CM or (D) CM from MCF7-Neo and MCF7-Snail was analyzed using ImageJ Fiji Just software. Statistical analyses were done using GraphPad Prism software (one-way ANOVA, Šídák's multiple comparisons test, ****p< 0.0001, ***p< 0.001, **p < 0.01, *p < 0.05). Bars represent the SD of the mean. Results are representative of 3 experiments performed independently.
Human Mouse Rat Neural Progenitor Cell Marker Antibody Panel, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/progenitor+cells/pmc07387844-48-10-22?v=R%26D+Systems
Average 93 stars, based on 1 article reviews
human mouse rat neural progenitor cell marker antibody panel - by Bioz Stars, 2026-08
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99
ATCC xcl1 dcxpgfp
Human Neural <t>Progenitor</t> Cells (NPCs) display increased neurite outgrowth when cultured with exosomes and CM from MCF-7 Snail cells compared to MCF-7 Neo. MCF-7 Neo or MCF-7 Snail was cultured in exosome-depleted medium (Exo-D medium) for 3 days, and conditioned medium (CM) was collected, or exosomes were isolated from the CM. These were subsequently cultured with NPCs for 2 days. (A) Images of NPC after incubation in NPC regular medium, Exo-D medium, exosomes or CM with or without Talin1 inhibitor mH4 were captured with a Nikon Eclipse TE2000-S Inverted Fluorescence Microscope. (B) The percentage of NPCs with neurite outgrowth and average neuron length was measured utilizing Image J Fiji Just software in NPCs cultured with NPC medium, Exo-D medium, and Exo-D medium plus NGF-beta as a positive control. The percentage of NPCs with neurite outgrowth and average neuron length of NPCs cultured with (C) exosomes isolated from MCF7-Neo and MCF7-Snail CM or (D) CM from MCF7-Neo and MCF7-Snail was analyzed using ImageJ Fiji Just software. Statistical analyses were done using GraphPad Prism software (one-way ANOVA, Šídák's multiple comparisons test, ****p< 0.0001, ***p< 0.001, **p < 0.01, *p < 0.05). Bars represent the SD of the mean. Results are representative of 3 experiments performed independently.
Xcl1 Dcxpgfp, 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/progenitor+cells/pm41807428-76-20-23?v=ATCC
Average 99 stars, based on 1 article reviews
xcl1 dcxpgfp - by Bioz Stars, 2026-08
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93
ATCC c666 1 acs5006
Human Neural <t>Progenitor</t> Cells (NPCs) display increased neurite outgrowth when cultured with exosomes and CM from MCF-7 Snail cells compared to MCF-7 Neo. MCF-7 Neo or MCF-7 Snail was cultured in exosome-depleted medium (Exo-D medium) for 3 days, and conditioned medium (CM) was collected, or exosomes were isolated from the CM. These were subsequently cultured with NPCs for 2 days. (A) Images of NPC after incubation in NPC regular medium, Exo-D medium, exosomes or CM with or without Talin1 inhibitor mH4 were captured with a Nikon Eclipse TE2000-S Inverted Fluorescence Microscope. (B) The percentage of NPCs with neurite outgrowth and average neuron length was measured utilizing Image J Fiji Just software in NPCs cultured with NPC medium, Exo-D medium, and Exo-D medium plus NGF-beta as a positive control. The percentage of NPCs with neurite outgrowth and average neuron length of NPCs cultured with (C) exosomes isolated from MCF7-Neo and MCF7-Snail CM or (D) CM from MCF7-Neo and MCF7-Snail was analyzed using ImageJ Fiji Just software. Statistical analyses were done using GraphPad Prism software (one-way ANOVA, Šídák's multiple comparisons test, ****p< 0.0001, ***p< 0.001, **p < 0.01, *p < 0.05). Bars represent the SD of the mean. Results are representative of 3 experiments performed independently.
C666 1 Acs5006, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/progenitor+cells/pm38698443-110-14-26?v=ATCC
Average 93 stars, based on 1 article reviews
c666 1 acs5006 - by Bioz Stars, 2026-08
93/100 stars
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94
ATCC neural progenitor cell expansion kit supplements
Human Neural <t>Progenitor</t> Cells (NPCs) display increased neurite outgrowth when cultured with exosomes and CM from MCF-7 Snail cells compared to MCF-7 Neo. MCF-7 Neo or MCF-7 Snail was cultured in exosome-depleted medium (Exo-D medium) for 3 days, and conditioned medium (CM) was collected, or exosomes were isolated from the CM. These were subsequently cultured with NPCs for 2 days. (A) Images of NPC after incubation in NPC regular medium, Exo-D medium, exosomes or CM with or without Talin1 inhibitor mH4 were captured with a Nikon Eclipse TE2000-S Inverted Fluorescence Microscope. (B) The percentage of NPCs with neurite outgrowth and average neuron length was measured utilizing Image J Fiji Just software in NPCs cultured with NPC medium, Exo-D medium, and Exo-D medium plus NGF-beta as a positive control. The percentage of NPCs with neurite outgrowth and average neuron length of NPCs cultured with (C) exosomes isolated from MCF7-Neo and MCF7-Snail CM or (D) CM from MCF7-Neo and MCF7-Snail was analyzed using ImageJ Fiji Just software. Statistical analyses were done using GraphPad Prism software (one-way ANOVA, Šídák's multiple comparisons test, ****p< 0.0001, ***p< 0.001, **p < 0.01, *p < 0.05). Bars represent the SD of the mean. Results are representative of 3 experiments performed independently.
Neural Progenitor Cell Expansion Kit Supplements, supplied by ATCC, 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/progenitor+cells/pm30181550-234-30-36?v=ATCC
Average 94 stars, based on 1 article reviews
neural progenitor cell expansion kit supplements - by Bioz Stars, 2026-08
94/100 stars
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92
Proteintech btk polyclonal antibody
Human Neural <t>Progenitor</t> Cells (NPCs) display increased neurite outgrowth when cultured with exosomes and CM from MCF-7 Snail cells compared to MCF-7 Neo. MCF-7 Neo or MCF-7 Snail was cultured in exosome-depleted medium (Exo-D medium) for 3 days, and conditioned medium (CM) was collected, or exosomes were isolated from the CM. These were subsequently cultured with NPCs for 2 days. (A) Images of NPC after incubation in NPC regular medium, Exo-D medium, exosomes or CM with or without Talin1 inhibitor mH4 were captured with a Nikon Eclipse TE2000-S Inverted Fluorescence Microscope. (B) The percentage of NPCs with neurite outgrowth and average neuron length was measured utilizing Image J Fiji Just software in NPCs cultured with NPC medium, Exo-D medium, and Exo-D medium plus NGF-beta as a positive control. The percentage of NPCs with neurite outgrowth and average neuron length of NPCs cultured with (C) exosomes isolated from MCF7-Neo and MCF7-Snail CM or (D) CM from MCF7-Neo and MCF7-Snail was analyzed using ImageJ Fiji Just software. Statistical analyses were done using GraphPad Prism software (one-way ANOVA, Šídák's multiple comparisons test, ****p< 0.0001, ***p< 0.001, **p < 0.01, *p < 0.05). Bars represent the SD of the mean. Results are representative of 3 experiments performed independently.
Btk Polyclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/progenitor+cells/pmc07447306-111-21-28?v=Proteintech
Average 92 stars, based on 1 article reviews
btk polyclonal antibody - by Bioz Stars, 2026-08
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93
Boster Bio cd34
DIF of <t>CD34/α-SMA</t> in 1-month-old goat testis. ( A-C ) DIF of <t>CD34/α-SMA</t> in 1-month-old goat testis; ( D-F ) DIF of CD34/α-SMA in blood vessels of 1-month-old goat testis; CD34 (red); α-SMA (green); DAPI (blue); CD34 + cells (white triangular arrows); ST. Seminiferous tubule; BV. Blood vessels. Scale bar = ( A-C ):10 μm; ( D-F ): 20 μm.
Cd34, supplied by Boster Bio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/progenitor+cells/pmc12894951-46-6-9?v=Boster+Bio
Average 93 stars, based on 1 article reviews
cd34 - by Bioz Stars, 2026-08
93/100 stars
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90
Miltenyi Biotec macs
DIF of <t>CD34/α-SMA</t> in 1-month-old goat testis. ( A-C ) DIF of <t>CD34/α-SMA</t> in 1-month-old goat testis; ( D-F ) DIF of CD34/α-SMA in blood vessels of 1-month-old goat testis; CD34 (red); α-SMA (green); DAPI (blue); CD34 + cells (white triangular arrows); ST. Seminiferous tubule; BV. Blood vessels. Scale bar = ( A-C ):10 μm; ( D-F ): 20 μm.
Macs, supplied by Miltenyi Biotec, 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/progenitor+cells/pmc06928864-153-10-21?v=Miltenyi+Biotec
Average 90 stars, based on 1 article reviews
macs - by Bioz Stars, 2026-08
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93
R&D Systems human neural progenitor cell marker antibody panel
DIF of <t>CD34/α-SMA</t> in 1-month-old goat testis. ( A-C ) DIF of <t>CD34/α-SMA</t> in 1-month-old goat testis; ( D-F ) DIF of CD34/α-SMA in blood vessels of 1-month-old goat testis; CD34 (red); α-SMA (green); DAPI (blue); CD34 + cells (white triangular arrows); ST. Seminiferous tubule; BV. Blood vessels. Scale bar = ( A-C ):10 μm; ( D-F ): 20 μm.
Human Neural Progenitor Cell Marker Antibody Panel, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/progenitor+cells/10__4103_slash_nrr__nrr___d___24___01178-52-28-36?v=R%26D+Systems
Average 93 stars, based on 1 article reviews
human neural progenitor cell marker antibody panel - by Bioz Stars, 2026-08
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Image Search Results


Fig. 2 O‑GlcNAcylation weakens FTO expression. (A) Volcano diagram representing FTO expression after OSMI-1 treatment in KG1a cells; p-val ue < 0.05,|Fold change| > 1.5. (B) The correlation between O-GlcNAc levels and the survival of AML patients was explored using upper quartile analysis through the Kaplan-Meier Plotter. (C) The association between O-GlcNAc and FTO in a cohort of 14 MDS/AML patients by ELISA. (D) Western blot detec tion of FTO level in cKit + cells of the bone marrow from MLL-AF9-induced leukemia mice. (E) FTO level in primary CD34 + cells from MDS/AML patients after 20 µM DMSO and 20 µg/mL OSMI-1 treatment. (F-G) FTO level in KG1a and SKM1 cells after TMG and OSMI-1 treatment

Journal: Cell communication and signaling : CCS

Article Title: O-GlcNAcylated FTO promotes m6A modification of SOX4 to enhance MDS/AML cell proliferation.

doi: 10.1186/s12964-025-02058-6

Figure Lengend Snippet: Fig. 2 O‑GlcNAcylation weakens FTO expression. (A) Volcano diagram representing FTO expression after OSMI-1 treatment in KG1a cells; p-val ue < 0.05,|Fold change| > 1.5. (B) The correlation between O-GlcNAc levels and the survival of AML patients was explored using upper quartile analysis through the Kaplan-Meier Plotter. (C) The association between O-GlcNAc and FTO in a cohort of 14 MDS/AML patients by ELISA. (D) Western blot detec tion of FTO level in cKit + cells of the bone marrow from MLL-AF9-induced leukemia mice. (E) FTO level in primary CD34 + cells from MDS/AML patients after 20 µM DMSO and 20 µg/mL OSMI-1 treatment. (F-G) FTO level in KG1a and SKM1 cells after TMG and OSMI-1 treatment

Article Snippet: CD34+ cells were treated with 20 μM DMSO and 20 μg/mL OSMI-1 (MCE, NJ, USA) for 48 h, respectively.

Techniques: Expressing, Enzyme-linked Immunosorbent Assay, Western Blot

Human Neural Progenitor Cells (NPCs) display increased neurite outgrowth when cultured with exosomes and CM from MCF-7 Snail cells compared to MCF-7 Neo. MCF-7 Neo or MCF-7 Snail was cultured in exosome-depleted medium (Exo-D medium) for 3 days, and conditioned medium (CM) was collected, or exosomes were isolated from the CM. These were subsequently cultured with NPCs for 2 days. (A) Images of NPC after incubation in NPC regular medium, Exo-D medium, exosomes or CM with or without Talin1 inhibitor mH4 were captured with a Nikon Eclipse TE2000-S Inverted Fluorescence Microscope. (B) The percentage of NPCs with neurite outgrowth and average neuron length was measured utilizing Image J Fiji Just software in NPCs cultured with NPC medium, Exo-D medium, and Exo-D medium plus NGF-beta as a positive control. The percentage of NPCs with neurite outgrowth and average neuron length of NPCs cultured with (C) exosomes isolated from MCF7-Neo and MCF7-Snail CM or (D) CM from MCF7-Neo and MCF7-Snail was analyzed using ImageJ Fiji Just software. Statistical analyses were done using GraphPad Prism software (one-way ANOVA, Šídák's multiple comparisons test, ****p< 0.0001, ***p< 0.001, **p < 0.01, *p < 0.05). Bars represent the SD of the mean. Results are representative of 3 experiments performed independently.

Journal: Journal of Cancer

Article Title: Talin1 Mediates Tumor-Nerve Interactions in Prostate and Breast Cancer Cells

doi: 10.7150/jca.127292

Figure Lengend Snippet: Human Neural Progenitor Cells (NPCs) display increased neurite outgrowth when cultured with exosomes and CM from MCF-7 Snail cells compared to MCF-7 Neo. MCF-7 Neo or MCF-7 Snail was cultured in exosome-depleted medium (Exo-D medium) for 3 days, and conditioned medium (CM) was collected, or exosomes were isolated from the CM. These were subsequently cultured with NPCs for 2 days. (A) Images of NPC after incubation in NPC regular medium, Exo-D medium, exosomes or CM with or without Talin1 inhibitor mH4 were captured with a Nikon Eclipse TE2000-S Inverted Fluorescence Microscope. (B) The percentage of NPCs with neurite outgrowth and average neuron length was measured utilizing Image J Fiji Just software in NPCs cultured with NPC medium, Exo-D medium, and Exo-D medium plus NGF-beta as a positive control. The percentage of NPCs with neurite outgrowth and average neuron length of NPCs cultured with (C) exosomes isolated from MCF7-Neo and MCF7-Snail CM or (D) CM from MCF7-Neo and MCF7-Snail was analyzed using ImageJ Fiji Just software. Statistical analyses were done using GraphPad Prism software (one-way ANOVA, Šídák's multiple comparisons test, ****p< 0.0001, ***p< 0.001, **p < 0.01, *p < 0.05). Bars represent the SD of the mean. Results are representative of 3 experiments performed independently.

Article Snippet: Neural Progenitor Cells (ACS-5004), NPC Growth Medium (ATCC ACS-3003), DMEM: F12 (ATCC 30-2006) and Cell Basement Membrane (ACS-3035) were purchased from American Tissue Cell Culture (ATCC), Manassas, VA. Talin1 inhibitor, mH4 and F3 protease inhibitor control, was obtained from Dr. Kensei Tsuzaka, Kaytee Bio, Co. & Ltd., Chiba, Japan. mH4 was dissolved in DMSO to a stock solution of 14 mg/ml.

Techniques: Cell Culture, Isolation, Incubation, Fluorescence, Microscopy, Software, Positive Control

Human neural progenitor cells (NPCs) display reduced neurite outgrowth with exosomes and CM from C4-2 Snail knockdown (C4-2 E8) cells compared to C4-2 Non-silencing (NS) cells. C4-2 NS or C4-2 E8 was cultured in exosome-depleted medium (Exo-D medium) for 3 days, and conditioned medium (CM) was collected, or exosomes were isolated from the CM. These were subsequently cultured with NPCs for 2 days. (A) Images of NPC after incubation in NPC regular medium, Exo-D medium, exosomes, or CM with or without Talin1 inhibitor mH4 were captured with a Nikon Eclipse TE2000-S Inverted Fluorescence Microscope. The percentage of NPCs with neurite outgrowth and average neuron length of NPCs cultured with (B) exosomes isolated from MCF7-Neo and MCF7-Snail CM or (C) CM from MCF7-Neo and MCF7-Snail was analyzed using ImageJ Fiji Just software. Statistical analyses were done using GraphPad Prism software (one-way ANOVA, Šídák's multiple comparisons test, ****p< 0.0001, **p < 0.01, *p < 0.05). Bars represent the SD of the mean. Results are representative of 3 experiments performed independently.

Journal: Journal of Cancer

Article Title: Talin1 Mediates Tumor-Nerve Interactions in Prostate and Breast Cancer Cells

doi: 10.7150/jca.127292

Figure Lengend Snippet: Human neural progenitor cells (NPCs) display reduced neurite outgrowth with exosomes and CM from C4-2 Snail knockdown (C4-2 E8) cells compared to C4-2 Non-silencing (NS) cells. C4-2 NS or C4-2 E8 was cultured in exosome-depleted medium (Exo-D medium) for 3 days, and conditioned medium (CM) was collected, or exosomes were isolated from the CM. These were subsequently cultured with NPCs for 2 days. (A) Images of NPC after incubation in NPC regular medium, Exo-D medium, exosomes, or CM with or without Talin1 inhibitor mH4 were captured with a Nikon Eclipse TE2000-S Inverted Fluorescence Microscope. The percentage of NPCs with neurite outgrowth and average neuron length of NPCs cultured with (B) exosomes isolated from MCF7-Neo and MCF7-Snail CM or (C) CM from MCF7-Neo and MCF7-Snail was analyzed using ImageJ Fiji Just software. Statistical analyses were done using GraphPad Prism software (one-way ANOVA, Šídák's multiple comparisons test, ****p< 0.0001, **p < 0.01, *p < 0.05). Bars represent the SD of the mean. Results are representative of 3 experiments performed independently.

Article Snippet: Neural Progenitor Cells (ACS-5004), NPC Growth Medium (ATCC ACS-3003), DMEM: F12 (ATCC 30-2006) and Cell Basement Membrane (ACS-3035) were purchased from American Tissue Cell Culture (ATCC), Manassas, VA. Talin1 inhibitor, mH4 and F3 protease inhibitor control, was obtained from Dr. Kensei Tsuzaka, Kaytee Bio, Co. & Ltd., Chiba, Japan. mH4 was dissolved in DMSO to a stock solution of 14 mg/ml.

Techniques: Knockdown, Cell Culture, Isolation, Incubation, Fluorescence, Microscopy, Software

DIF of CD34/α-SMA in 1-month-old goat testis. ( A-C ) DIF of CD34/α-SMA in 1-month-old goat testis; ( D-F ) DIF of CD34/α-SMA in blood vessels of 1-month-old goat testis; CD34 (red); α-SMA (green); DAPI (blue); CD34 + cells (white triangular arrows); ST. Seminiferous tubule; BV. Blood vessels. Scale bar = ( A-C ):10 μm; ( D-F ): 20 μm.

Journal: Scientific Reports

Article Title: Analysis of the spatial-temporal distribution and functional morphology of telocytes in goat testes

doi: 10.1038/s41598-026-36639-3

Figure Lengend Snippet: DIF of CD34/α-SMA in 1-month-old goat testis. ( A-C ) DIF of CD34/α-SMA in 1-month-old goat testis; ( D-F ) DIF of CD34/α-SMA in blood vessels of 1-month-old goat testis; CD34 (red); α-SMA (green); DAPI (blue); CD34 + cells (white triangular arrows); ST. Seminiferous tubule; BV. Blood vessels. Scale bar = ( A-C ):10 μm; ( D-F ): 20 μm.

Article Snippet: The antibody pairs were as follows: CD34 (1:100, BA3414, Boster Biological Technology Co., Ltd)/α-SMA (1:100, BM0002, Boster Biological Technology Co., Ltd), CD34 (1:100)/Vimentin (1:100, BM0135, Boster Biological Technology Co., Ltd), α-SMA (1:100)/PDGFR-α (1:100, 3174 S, CellSignaling Technology).

Techniques:

DIF of CD34/α-SMA in 2-month-old goat testis. ( A-C ) DIF of CD34/α-SMA in 2-month-old goat testis; ( D-F ) DIF of CD34/α-SMA in blood vessels of 2-month-old goat testis; CD34 (red); α-SMA (green); DAPI (blue); CD34 + cells (white triangular arrows); ST. Seminiferous tubule; BV. Blood vessels. Scale bar = ( A-C ): 20 μm; ( D-F ): 10 μm.

Journal: Scientific Reports

Article Title: Analysis of the spatial-temporal distribution and functional morphology of telocytes in goat testes

doi: 10.1038/s41598-026-36639-3

Figure Lengend Snippet: DIF of CD34/α-SMA in 2-month-old goat testis. ( A-C ) DIF of CD34/α-SMA in 2-month-old goat testis; ( D-F ) DIF of CD34/α-SMA in blood vessels of 2-month-old goat testis; CD34 (red); α-SMA (green); DAPI (blue); CD34 + cells (white triangular arrows); ST. Seminiferous tubule; BV. Blood vessels. Scale bar = ( A-C ): 20 μm; ( D-F ): 10 μm.

Article Snippet: The antibody pairs were as follows: CD34 (1:100, BA3414, Boster Biological Technology Co., Ltd)/α-SMA (1:100, BM0002, Boster Biological Technology Co., Ltd), CD34 (1:100)/Vimentin (1:100, BM0135, Boster Biological Technology Co., Ltd), α-SMA (1:100)/PDGFR-α (1:100, 3174 S, CellSignaling Technology).

Techniques:

DIF of CD34/α-SMA in 12-month-old goat testis. ( A-I ) DIF of CD34/α-SMA in 12-month-old goat testis; ( J-L ) DIF of CD34/α-SMA in blood vessels of 12-month-old goat testis; CD34 (red); α-SMA (green); DAPI (blue); ST. Seminiferous tubule; BV. Blood vessels. Scale bar = ( A-F, J-L ): 10 μm; ( G-I ): 20 μm.

Journal: Scientific Reports

Article Title: Analysis of the spatial-temporal distribution and functional morphology of telocytes in goat testes

doi: 10.1038/s41598-026-36639-3

Figure Lengend Snippet: DIF of CD34/α-SMA in 12-month-old goat testis. ( A-I ) DIF of CD34/α-SMA in 12-month-old goat testis; ( J-L ) DIF of CD34/α-SMA in blood vessels of 12-month-old goat testis; CD34 (red); α-SMA (green); DAPI (blue); ST. Seminiferous tubule; BV. Blood vessels. Scale bar = ( A-F, J-L ): 10 μm; ( G-I ): 20 μm.

Article Snippet: The antibody pairs were as follows: CD34 (1:100, BA3414, Boster Biological Technology Co., Ltd)/α-SMA (1:100, BM0002, Boster Biological Technology Co., Ltd), CD34 (1:100)/Vimentin (1:100, BM0135, Boster Biological Technology Co., Ltd), α-SMA (1:100)/PDGFR-α (1:100, 3174 S, CellSignaling Technology).

Techniques:

DIF of CD34/ Vimentin in 1-month-old goat testis. ( A-C ) DIF of CD34/ Vimentin in 1-month-old goat testis. (1-a), (1-b), (1-c) are respectively enlarged images of (1) in ( A ), ( B ), ( C ). (2-a), (2-b) and (2-c) are the enlarged images of (2) in ( A ), ( B ) and ( C ) respectively. CD34 (red); α-SMA (green); DAPI (blue); TC (yellow, indicated by white triangular arrows); ST. Seminiferous tubule; SC. Sertoli cells. Scale bar = ( A, B, C ): 20 μm; (1 - a) - (1 - c), (2- a) - (2 - c): 10 μm.

Journal: Scientific Reports

Article Title: Analysis of the spatial-temporal distribution and functional morphology of telocytes in goat testes

doi: 10.1038/s41598-026-36639-3

Figure Lengend Snippet: DIF of CD34/ Vimentin in 1-month-old goat testis. ( A-C ) DIF of CD34/ Vimentin in 1-month-old goat testis. (1-a), (1-b), (1-c) are respectively enlarged images of (1) in ( A ), ( B ), ( C ). (2-a), (2-b) and (2-c) are the enlarged images of (2) in ( A ), ( B ) and ( C ) respectively. CD34 (red); α-SMA (green); DAPI (blue); TC (yellow, indicated by white triangular arrows); ST. Seminiferous tubule; SC. Sertoli cells. Scale bar = ( A, B, C ): 20 μm; (1 - a) - (1 - c), (2- a) - (2 - c): 10 μm.

Article Snippet: The antibody pairs were as follows: CD34 (1:100, BA3414, Boster Biological Technology Co., Ltd)/α-SMA (1:100, BM0002, Boster Biological Technology Co., Ltd), CD34 (1:100)/Vimentin (1:100, BM0135, Boster Biological Technology Co., Ltd), α-SMA (1:100)/PDGFR-α (1:100, 3174 S, CellSignaling Technology).

Techniques:

DIF of CD34/ Vimentin in 2-month-old goat testis. ( A-C ) DIF of CD34/ Vimentin in 2-month-old goat testis. (a-c) are enlarged views of the boxed areas in ( A-C ). CD34 (red); α-SMA (green); DAPI (blue); TC (yellow, indicated by white triangular arrows); ST. Seminiferous tubule. Scale bar = ( A-C ): 20 μm; (a-c): 10 μm.

Journal: Scientific Reports

Article Title: Analysis of the spatial-temporal distribution and functional morphology of telocytes in goat testes

doi: 10.1038/s41598-026-36639-3

Figure Lengend Snippet: DIF of CD34/ Vimentin in 2-month-old goat testis. ( A-C ) DIF of CD34/ Vimentin in 2-month-old goat testis. (a-c) are enlarged views of the boxed areas in ( A-C ). CD34 (red); α-SMA (green); DAPI (blue); TC (yellow, indicated by white triangular arrows); ST. Seminiferous tubule. Scale bar = ( A-C ): 20 μm; (a-c): 10 μm.

Article Snippet: The antibody pairs were as follows: CD34 (1:100, BA3414, Boster Biological Technology Co., Ltd)/α-SMA (1:100, BM0002, Boster Biological Technology Co., Ltd), CD34 (1:100)/Vimentin (1:100, BM0135, Boster Biological Technology Co., Ltd), α-SMA (1:100)/PDGFR-α (1:100, 3174 S, CellSignaling Technology).

Techniques:

DIF of CD34/ Vimentin in 12-month-old goat testis. ( A-C ) DIF of CD34/ Vimentin in 12-month-old goat testis. CD34 (red); Vimentin (green); DAPI (blue); ST. Seminiferous tubule; S. sperm; PS. Primary spermatocyte; SC. Sertoli cells; RS. Round sperm cells; White triangular arrows. Peritubular myoid cell nucleus. Scale bar = ( A-C ): 10 μm.

Journal: Scientific Reports

Article Title: Analysis of the spatial-temporal distribution and functional morphology of telocytes in goat testes

doi: 10.1038/s41598-026-36639-3

Figure Lengend Snippet: DIF of CD34/ Vimentin in 12-month-old goat testis. ( A-C ) DIF of CD34/ Vimentin in 12-month-old goat testis. CD34 (red); Vimentin (green); DAPI (blue); ST. Seminiferous tubule; S. sperm; PS. Primary spermatocyte; SC. Sertoli cells; RS. Round sperm cells; White triangular arrows. Peritubular myoid cell nucleus. Scale bar = ( A-C ): 10 μm.

Article Snippet: The antibody pairs were as follows: CD34 (1:100, BA3414, Boster Biological Technology Co., Ltd)/α-SMA (1:100, BM0002, Boster Biological Technology Co., Ltd), CD34 (1:100)/Vimentin (1:100, BM0135, Boster Biological Technology Co., Ltd), α-SMA (1:100)/PDGFR-α (1:100, 3174 S, CellSignaling Technology).

Techniques:

DIF of CD34/ Vimentin in 12-month-old goat testis. ( A-C ) DIF of CD34/ Vimentin in 12-month-old goat testis. (a-c) is an enlarged view of the white dotted box area of ( A-C ). CD34 (red); Vimentin (green); DAPI (blue); TC (yellow, indicated by white triangular arrows). Scale bar = ( A-C ), (a-c): 20 μm.

Journal: Scientific Reports

Article Title: Analysis of the spatial-temporal distribution and functional morphology of telocytes in goat testes

doi: 10.1038/s41598-026-36639-3

Figure Lengend Snippet: DIF of CD34/ Vimentin in 12-month-old goat testis. ( A-C ) DIF of CD34/ Vimentin in 12-month-old goat testis. (a-c) is an enlarged view of the white dotted box area of ( A-C ). CD34 (red); Vimentin (green); DAPI (blue); TC (yellow, indicated by white triangular arrows). Scale bar = ( A-C ), (a-c): 20 μm.

Article Snippet: The antibody pairs were as follows: CD34 (1:100, BA3414, Boster Biological Technology Co., Ltd)/α-SMA (1:100, BM0002, Boster Biological Technology Co., Ltd), CD34 (1:100)/Vimentin (1:100, BM0135, Boster Biological Technology Co., Ltd), α-SMA (1:100)/PDGFR-α (1:100, 3174 S, CellSignaling Technology).

Techniques:

DIF of CD34/ Vimentin in 12-month-old goat testis. ( A-C ) DIF of CD34/ Vimentin in 12-month-old goat testis. (1-a), (1-b), (1-c) are respectively enlarged images of (1) in ( A-C ). (2-a), (2-b), (2-c) are the enlarged images of (2) in ( A-C ). CD34 (red); Vimentin (green); DAPI (blue); TC (yellow); White triangular arrows. Peritubular myoid cell nucleus. Scale bar = ( A-C ): 50 μm; (1-a) - (1-c), (2-a) - (2-c): 10 μm.

Journal: Scientific Reports

Article Title: Analysis of the spatial-temporal distribution and functional morphology of telocytes in goat testes

doi: 10.1038/s41598-026-36639-3

Figure Lengend Snippet: DIF of CD34/ Vimentin in 12-month-old goat testis. ( A-C ) DIF of CD34/ Vimentin in 12-month-old goat testis. (1-a), (1-b), (1-c) are respectively enlarged images of (1) in ( A-C ). (2-a), (2-b), (2-c) are the enlarged images of (2) in ( A-C ). CD34 (red); Vimentin (green); DAPI (blue); TC (yellow); White triangular arrows. Peritubular myoid cell nucleus. Scale bar = ( A-C ): 50 μm; (1-a) - (1-c), (2-a) - (2-c): 10 μm.

Article Snippet: The antibody pairs were as follows: CD34 (1:100, BA3414, Boster Biological Technology Co., Ltd)/α-SMA (1:100, BM0002, Boster Biological Technology Co., Ltd), CD34 (1:100)/Vimentin (1:100, BM0135, Boster Biological Technology Co., Ltd), α-SMA (1:100)/PDGFR-α (1:100, 3174 S, CellSignaling Technology).

Techniques: