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cy3 labelit kit  (Mirus Bio)


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    Structured Review

    Mirus Bio cy3 labelit kit
    Cy3 Labelit Kit, supplied by Mirus Bio, used in various techniques. Bioz Stars score: 96/100, based on 1903 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cy3+kit/Label+IT+Nucleic+Acid+Labeling+Kit/pm42003491-71-6-9
    Average 96 stars, based on 1903 article reviews
    cy3 labelit kit - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Labeling:

    Article Title: Improved DNA binding to a type IV minor pilin increases natural transformation
    Article Snippet: .. For DNA localization experiments, 100 μl of overnight cultures grown in M63CA + G were co-incubated with 25 μg/ml AF488-mal and 100 ng of fluorescently labeled DNA for 30 min. Fluorescent DNA Cy3 was made from an ∼7 kb Δ pilT :: spec PCR product that was fluorescently labeled as described previously [ ] using the Cy3 LabelIT kit (Mirus Biosciences) as per the manufacturer's recommendations. ..

    Article Title: Stimulated Trafficking of RNAi to Parathyroid toward Its Angiogenetic Vessels for Suppressed Secretion of Parathyroid Hormone
    Article Snippet: Secondary hyperparathyroidism is driven by pathological overproduction of parathyroid hormone.. Surgery is invasive, drug therapy offers only transient control, and both carry substantial side effects.. Previous efforts to deliver siRNA to the parathyroid glands achieved only marginal efficacy because the constructs lacked a targeting ligand to overcome the organ’s limited vascular permeability and were rapidly cleared by renal filtration.

    Article Title: Silica-coated polyion complexes for enhanced pulmonary messenger RNA delivery with optimized silica layer stability.
    Article Snippet: .. Label IT® Nucleic Acid Labeling Kit (Cy3) and Label IT® Nucleic Acid Labeling Kit (Cy5) were purchased from Mirus Bio. (Madison, WI, USA). .. Econo-Pac 10 DG Desalting Columns was purchased from Bio-Rad Laboratories (Hercules, CA, USA).

    Polymerase Chain Reaction:

    Article Title: Improved DNA binding to a type IV minor pilin increases natural transformation
    Article Snippet: .. For DNA localization experiments, 100 μl of overnight cultures grown in M63CA + G were co-incubated with 25 μg/ml AF488-mal and 100 ng of fluorescently labeled DNA for 30 min. Fluorescent DNA Cy3 was made from an ∼7 kb Δ pilT :: spec PCR product that was fluorescently labeled as described previously [ ] using the Cy3 LabelIT kit (Mirus Biosciences) as per the manufacturer's recommendations. ..

    Article Title: Cell penetrating peptide-functionalized small interfering RNA nanoparticles knock down HER expression in breast cancer cells
    Article Snippet: Other reagents were sourced as follows: siRNA (Integrated DNA Technologies), sense sequences of siEGFP: 5′-GGCUACGUCCAGGAGCGCACC-3′, siHer3: 5′-ACCACGGUAUCUGGUCAUAAA-3′, siHer2: 5′-GGUGCU UGGAUCUGGCGCUUU-3′; primer sequences: ERBB2/HER2: forward: GGAAGTACACGATGCGGAGACT, reverse: ACCTTCCTCAGCTCCGTCTCTT; ERBB3/HER3: forward: CTATGAGGCGATACTTGGAACGG, reverse: GCACAGTTCCAAAGACACCCG; ACTB: forward: CACCATTGGCAATGAGCGGTTC, reverse: AGGTCTTTGCGGATGTCCACGT. .. RNA isolation: Aurum Total RNA Mini Kit (Bio-Rad), cDNA synthesis: iScript cDNA Synthesis Kit (Bio-Rad), polymerase chain reaction (PCR): Prime PCR supermix (Bio-Rad), Lipofectamine RNAiMax (Sigma), RNA quantification: QuantiFluor DNA quantification kit (Promega), Protamine sulfate from salmon Grade X (Sigma), Label IT siRNA localization kit Cy3 (Mirus Bio), primary and secondary antibodies (Cedarlane). .. Dulbecco’s modified Eagle’s medium (Fisher Scientific), FBS (Fisher Scientific), OptiMEM (Gibco), nuclease free water (Gibco), RIPA buffer (Fisher Scientific), unfractionated heparin (Fisher Scientific), chloroquine (CQ) HCl (Fisher Scientific), BSA protein quantification kit (Fisher Scientific), SYBR Safe nucleic acid stain, 0.25% trypsin-EDTA (VWR Life Sciences), CellTiter 96 AQueous Cell Proliferation Assay (Promega).

    Article Title: Cell penetrating peptide-functionalized small interfering RNA nanoparticles knock down HER expression in breast cancer cells.
    Article Snippet: Other reagents were sourced as follows: siRNA (Integrated DNA Technologies), sense sequences of siEGFP: 5′-GGCUACGUCCAGGAGCGCACC-3′, siHer3: 5′-ACCACGGUAUCUGGUCAUAAA-3′, siHer2: 5′-GGUGCU UGGAUCUGGCGCUUU-3′; primer sequences: ERBB2/HER2: forward: GGAAGTACACGATGCGGAGACT, reverse: ACCTTCCTCAGCTCCGTCTCTT; ERBB3/HER3: forward: CTATGAGGCGATACTTGGAACGG, reverse: GCACAGTTCCAAAGACACCCG; ACTB: forward: CACCATTGGCAATGAGCGGTTC, reverse: AGGTCTTTGCGGATGTCCACGT. .. RNA isolation: Aurum Total RNA Mini Kit (Bio-Rad), cDNA synthesis: iScript cDNA Synthesis Kit (Bio-Rad), polymerase chain reaction (PCR): Prime PCR supermix (Bio-Rad), Lipofectamine RNAiMax (Sigma), RNA quantification: QuantiFluor DNA quantification kit (Promega), Protamine sulfate from salmon Grade X (Sigma), Label IT siRNA localization kit Cy3 (Mirus Bio), primary and secondary antibodies (Cedarlane). .. Dulbecco’s modified Eagle’s medium (Fisher Scientific), FBS (Fisher Scientific), OptiMEM (Gibco), nuclease free water (Gibco), RIPA buffer (Fisher Scientific), unfractionated heparin (Fisher Scientific), chloroquine (CQ) HCl (Fisher Scientific), BSA protein quantification kit (Fisher Scientific), SYBR Safe nucleic acid stain, 0.25% trypsin-EDTA (VWR Life Sciences), CellTiter 96 AQueous Cell Proliferation Assay (Promega).

    Plasmid Preparation:

    Article Title: Peptide-assisted lipofection enables efficient non-viral delivery of large CRISPR/Cas9 constructs for genome editing applications.
    Article Snippet: As a cell cycle arrest inducer, aphidicolin was obtained from Merck. .. Label IT® Plasmid Delivery Control Cy3 (2700 bp, Mirus Bio), Hoechst 33342 (Invitrogen), and Lysotracker Green DND-26 (Invitrogen) were used for fluorescence-based analysis of PAL trafficking. ..

    Control:

    Article Title: Peptide-assisted lipofection enables efficient non-viral delivery of large CRISPR/Cas9 constructs for genome editing applications.
    Article Snippet: As a cell cycle arrest inducer, aphidicolin was obtained from Merck. .. Label IT® Plasmid Delivery Control Cy3 (2700 bp, Mirus Bio), Hoechst 33342 (Invitrogen), and Lysotracker Green DND-26 (Invitrogen) were used for fluorescence-based analysis of PAL trafficking. ..

    Fluorescence:

    Article Title: Peptide-assisted lipofection enables efficient non-viral delivery of large CRISPR/Cas9 constructs for genome editing applications.
    Article Snippet: As a cell cycle arrest inducer, aphidicolin was obtained from Merck. .. Label IT® Plasmid Delivery Control Cy3 (2700 bp, Mirus Bio), Hoechst 33342 (Invitrogen), and Lysotracker Green DND-26 (Invitrogen) were used for fluorescence-based analysis of PAL trafficking. ..

    Isolation:

    Article Title: Cell penetrating peptide-functionalized small interfering RNA nanoparticles knock down HER expression in breast cancer cells
    Article Snippet: Other reagents were sourced as follows: siRNA (Integrated DNA Technologies), sense sequences of siEGFP: 5′-GGCUACGUCCAGGAGCGCACC-3′, siHer3: 5′-ACCACGGUAUCUGGUCAUAAA-3′, siHer2: 5′-GGUGCU UGGAUCUGGCGCUUU-3′; primer sequences: ERBB2/HER2: forward: GGAAGTACACGATGCGGAGACT, reverse: ACCTTCCTCAGCTCCGTCTCTT; ERBB3/HER3: forward: CTATGAGGCGATACTTGGAACGG, reverse: GCACAGTTCCAAAGACACCCG; ACTB: forward: CACCATTGGCAATGAGCGGTTC, reverse: AGGTCTTTGCGGATGTCCACGT. .. RNA isolation: Aurum Total RNA Mini Kit (Bio-Rad), cDNA synthesis: iScript cDNA Synthesis Kit (Bio-Rad), polymerase chain reaction (PCR): Prime PCR supermix (Bio-Rad), Lipofectamine RNAiMax (Sigma), RNA quantification: QuantiFluor DNA quantification kit (Promega), Protamine sulfate from salmon Grade X (Sigma), Label IT siRNA localization kit Cy3 (Mirus Bio), primary and secondary antibodies (Cedarlane). .. Dulbecco’s modified Eagle’s medium (Fisher Scientific), FBS (Fisher Scientific), OptiMEM (Gibco), nuclease free water (Gibco), RIPA buffer (Fisher Scientific), unfractionated heparin (Fisher Scientific), chloroquine (CQ) HCl (Fisher Scientific), BSA protein quantification kit (Fisher Scientific), SYBR Safe nucleic acid stain, 0.25% trypsin-EDTA (VWR Life Sciences), CellTiter 96 AQueous Cell Proliferation Assay (Promega).

    Article Title: Cell penetrating peptide-functionalized small interfering RNA nanoparticles knock down HER expression in breast cancer cells.
    Article Snippet: Other reagents were sourced as follows: siRNA (Integrated DNA Technologies), sense sequences of siEGFP: 5′-GGCUACGUCCAGGAGCGCACC-3′, siHer3: 5′-ACCACGGUAUCUGGUCAUAAA-3′, siHer2: 5′-GGUGCU UGGAUCUGGCGCUUU-3′; primer sequences: ERBB2/HER2: forward: GGAAGTACACGATGCGGAGACT, reverse: ACCTTCCTCAGCTCCGTCTCTT; ERBB3/HER3: forward: CTATGAGGCGATACTTGGAACGG, reverse: GCACAGTTCCAAAGACACCCG; ACTB: forward: CACCATTGGCAATGAGCGGTTC, reverse: AGGTCTTTGCGGATGTCCACGT. .. RNA isolation: Aurum Total RNA Mini Kit (Bio-Rad), cDNA synthesis: iScript cDNA Synthesis Kit (Bio-Rad), polymerase chain reaction (PCR): Prime PCR supermix (Bio-Rad), Lipofectamine RNAiMax (Sigma), RNA quantification: QuantiFluor DNA quantification kit (Promega), Protamine sulfate from salmon Grade X (Sigma), Label IT siRNA localization kit Cy3 (Mirus Bio), primary and secondary antibodies (Cedarlane). .. Dulbecco’s modified Eagle’s medium (Fisher Scientific), FBS (Fisher Scientific), OptiMEM (Gibco), nuclease free water (Gibco), RIPA buffer (Fisher Scientific), unfractionated heparin (Fisher Scientific), chloroquine (CQ) HCl (Fisher Scientific), BSA protein quantification kit (Fisher Scientific), SYBR Safe nucleic acid stain, 0.25% trypsin-EDTA (VWR Life Sciences), CellTiter 96 AQueous Cell Proliferation Assay (Promega).

    cDNA Synthesis:

    Article Title: Cell penetrating peptide-functionalized small interfering RNA nanoparticles knock down HER expression in breast cancer cells
    Article Snippet: Other reagents were sourced as follows: siRNA (Integrated DNA Technologies), sense sequences of siEGFP: 5′-GGCUACGUCCAGGAGCGCACC-3′, siHer3: 5′-ACCACGGUAUCUGGUCAUAAA-3′, siHer2: 5′-GGUGCU UGGAUCUGGCGCUUU-3′; primer sequences: ERBB2/HER2: forward: GGAAGTACACGATGCGGAGACT, reverse: ACCTTCCTCAGCTCCGTCTCTT; ERBB3/HER3: forward: CTATGAGGCGATACTTGGAACGG, reverse: GCACAGTTCCAAAGACACCCG; ACTB: forward: CACCATTGGCAATGAGCGGTTC, reverse: AGGTCTTTGCGGATGTCCACGT. .. RNA isolation: Aurum Total RNA Mini Kit (Bio-Rad), cDNA synthesis: iScript cDNA Synthesis Kit (Bio-Rad), polymerase chain reaction (PCR): Prime PCR supermix (Bio-Rad), Lipofectamine RNAiMax (Sigma), RNA quantification: QuantiFluor DNA quantification kit (Promega), Protamine sulfate from salmon Grade X (Sigma), Label IT siRNA localization kit Cy3 (Mirus Bio), primary and secondary antibodies (Cedarlane). .. Dulbecco’s modified Eagle’s medium (Fisher Scientific), FBS (Fisher Scientific), OptiMEM (Gibco), nuclease free water (Gibco), RIPA buffer (Fisher Scientific), unfractionated heparin (Fisher Scientific), chloroquine (CQ) HCl (Fisher Scientific), BSA protein quantification kit (Fisher Scientific), SYBR Safe nucleic acid stain, 0.25% trypsin-EDTA (VWR Life Sciences), CellTiter 96 AQueous Cell Proliferation Assay (Promega).

    Article Title: Cell penetrating peptide-functionalized small interfering RNA nanoparticles knock down HER expression in breast cancer cells.
    Article Snippet: Other reagents were sourced as follows: siRNA (Integrated DNA Technologies), sense sequences of siEGFP: 5′-GGCUACGUCCAGGAGCGCACC-3′, siHer3: 5′-ACCACGGUAUCUGGUCAUAAA-3′, siHer2: 5′-GGUGCU UGGAUCUGGCGCUUU-3′; primer sequences: ERBB2/HER2: forward: GGAAGTACACGATGCGGAGACT, reverse: ACCTTCCTCAGCTCCGTCTCTT; ERBB3/HER3: forward: CTATGAGGCGATACTTGGAACGG, reverse: GCACAGTTCCAAAGACACCCG; ACTB: forward: CACCATTGGCAATGAGCGGTTC, reverse: AGGTCTTTGCGGATGTCCACGT. .. RNA isolation: Aurum Total RNA Mini Kit (Bio-Rad), cDNA synthesis: iScript cDNA Synthesis Kit (Bio-Rad), polymerase chain reaction (PCR): Prime PCR supermix (Bio-Rad), Lipofectamine RNAiMax (Sigma), RNA quantification: QuantiFluor DNA quantification kit (Promega), Protamine sulfate from salmon Grade X (Sigma), Label IT siRNA localization kit Cy3 (Mirus Bio), primary and secondary antibodies (Cedarlane). .. Dulbecco’s modified Eagle’s medium (Fisher Scientific), FBS (Fisher Scientific), OptiMEM (Gibco), nuclease free water (Gibco), RIPA buffer (Fisher Scientific), unfractionated heparin (Fisher Scientific), chloroquine (CQ) HCl (Fisher Scientific), BSA protein quantification kit (Fisher Scientific), SYBR Safe nucleic acid stain, 0.25% trypsin-EDTA (VWR Life Sciences), CellTiter 96 AQueous Cell Proliferation Assay (Promega).



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    Image Search Results


    (A) Representative immunofluorescence images showing the localization nascent transcripts (EU, green) inside the nucleus (blue) of early GV oocytes. Images show EU levels in negative control (no EU), control (with EU), upon treatment with α-amanitin, and triptolide. Scale bar: 10 µm. (B) Frequency of PSSC with α-amanitin measured by scoring the percentage of eggs with PSSC, similar to levels observed with triptolide . Plots show number of eggs analyzed on top. Statistical significance is measured by Fisher’s exact test, ns = not significant. (C) Representative time-lapse images showing the localization of MajSat RNA in GV and MI oocytes and MII eggs upon microinjection of GV oocytes with UTP-X-Cy3 labeled MajSat (top panel) and control (bottom panel) RNA. MajSat RNA localizes to the pericentromeres during metaphase I and metaphase II stages along with foci present in the cytoplasm. Cy3-labeled control RNA localizes only in the cytoplasm and not on chromosomes. MajSat and control RNA (green), chromosomes (H2B-SNAP, blue) are shown. Scale bars: 10 µm. (D) Co-localization of MajSat RNA and SGO1 observed on metaphase I chromosome spreads upon performing RNA FISH with immunofluorescence. Scale bar: 10 µm.

    Journal: bioRxiv

    Article Title: Restoring Shugoshin 1 reduces chromosome errors in human eggs

    doi: 10.64898/2026.01.08.698387

    Figure Lengend Snippet: (A) Representative immunofluorescence images showing the localization nascent transcripts (EU, green) inside the nucleus (blue) of early GV oocytes. Images show EU levels in negative control (no EU), control (with EU), upon treatment with α-amanitin, and triptolide. Scale bar: 10 µm. (B) Frequency of PSSC with α-amanitin measured by scoring the percentage of eggs with PSSC, similar to levels observed with triptolide . Plots show number of eggs analyzed on top. Statistical significance is measured by Fisher’s exact test, ns = not significant. (C) Representative time-lapse images showing the localization of MajSat RNA in GV and MI oocytes and MII eggs upon microinjection of GV oocytes with UTP-X-Cy3 labeled MajSat (top panel) and control (bottom panel) RNA. MajSat RNA localizes to the pericentromeres during metaphase I and metaphase II stages along with foci present in the cytoplasm. Cy3-labeled control RNA localizes only in the cytoplasm and not on chromosomes. MajSat and control RNA (green), chromosomes (H2B-SNAP, blue) are shown. Scale bars: 10 µm. (D) Co-localization of MajSat RNA and SGO1 observed on metaphase I chromosome spreads upon performing RNA FISH with immunofluorescence. Scale bar: 10 µm.

    Article Snippet: The HighYield T7 Cy3 RNA Labelling Kit (Jena Bioscience, #RNT-101-CY3) was used to label amplified sequences with Cy3-labelled UTP (UTP-X-Cy3, 35%), followed by DNA removal using TurboTM DNAse (ThermoFisher).

    Techniques: Immunofluorescence, Negative Control, Control, Microinjection, Labeling

    Effect of inflammation on spermatogonia in LPS-induced mouse testes. ( A ) Testes from LPS-induced mice (Orchitis) and the Sham group. n = 6 mice per group ( B ) Expression levels of SNHG1 and SP1 at the transcriptional level were detected using qPCR. n = 6 mice per group ( C ) Expression of SP1 at the protein level as detected by Western blot. n = 6 mice per group ( D ) H&E staining was used to analyze the histopathology of the testes. n = 3 mice per group ( E ) Apoptosis in testes was analyzed using TUNEL staining. n = 3 mice per group (F-I) Expression levels of Oct4, C-kit, IL-17 A and ZO-1 as detected by IHC assay. n = 3 mice per group. Statistical comparisons between the two groups were performed using an unpaired two-tailed Student’s t-test. *** P < 0.001

    Journal: Cellular and Molecular Life Sciences: CMLS

    Article Title: Inflammation-induced LncRNA SNHG1 orchestrates spermatogonium development in non-obstructive azoospermia via IL-17 A signaling pathway

    doi: 10.1007/s00018-025-06055-3

    Figure Lengend Snippet: Effect of inflammation on spermatogonia in LPS-induced mouse testes. ( A ) Testes from LPS-induced mice (Orchitis) and the Sham group. n = 6 mice per group ( B ) Expression levels of SNHG1 and SP1 at the transcriptional level were detected using qPCR. n = 6 mice per group ( C ) Expression of SP1 at the protein level as detected by Western blot. n = 6 mice per group ( D ) H&E staining was used to analyze the histopathology of the testes. n = 3 mice per group ( E ) Apoptosis in testes was analyzed using TUNEL staining. n = 3 mice per group (F-I) Expression levels of Oct4, C-kit, IL-17 A and ZO-1 as detected by IHC assay. n = 3 mice per group. Statistical comparisons between the two groups were performed using an unpaired two-tailed Student’s t-test. *** P < 0.001

    Article Snippet: For cell lines, the one-step TUNEL apoptosis assay kit with Cy3 (Beyotime, China) was used according to the manufacturer’s instructions.

    Techniques: Expressing, Western Blot, Staining, Histopathology, TUNEL Assay, Two Tailed Test

    Effects of LPS-induced inflammation on spermatogonia in vitro. (A) Cell proliferation was detected by EdU staining. (B-C) Apoptosis was detected using flow cytometry and the TUNEL assay. (D) SP1 expression at the protein level was detected using a Western blot. (E) Expression levels of SNHG1 and SP1 at the transcriptional level were detected using qPCR. (F–H) IF analysis of SP1 , C-kit, and Oct4 expression. All experiments were performed in at least triplicate. Statistical comparisons between the two groups were performed using an unpaired two-tailed Student’s t-test. ** P < 0.01, *** P < 0.001

    Journal: Cellular and Molecular Life Sciences: CMLS

    Article Title: Inflammation-induced LncRNA SNHG1 orchestrates spermatogonium development in non-obstructive azoospermia via IL-17 A signaling pathway

    doi: 10.1007/s00018-025-06055-3

    Figure Lengend Snippet: Effects of LPS-induced inflammation on spermatogonia in vitro. (A) Cell proliferation was detected by EdU staining. (B-C) Apoptosis was detected using flow cytometry and the TUNEL assay. (D) SP1 expression at the protein level was detected using a Western blot. (E) Expression levels of SNHG1 and SP1 at the transcriptional level were detected using qPCR. (F–H) IF analysis of SP1 , C-kit, and Oct4 expression. All experiments were performed in at least triplicate. Statistical comparisons between the two groups were performed using an unpaired two-tailed Student’s t-test. ** P < 0.01, *** P < 0.001

    Article Snippet: For cell lines, the one-step TUNEL apoptosis assay kit with Cy3 (Beyotime, China) was used according to the manufacturer’s instructions.

    Techniques: In Vitro, Staining, Flow Cytometry, TUNEL Assay, Expressing, Western Blot, Two Tailed Test

    SP1 knockdown reduces the LPS-induced spermatogonia dysfunction. ( A ) Cell proliferation was detected using EdU staining. ( B - C ) Cell apoptosis was detected using flow cytometry and the TUNEL assay. ( D ) Expression levels of SNHG1 and SP1 at the transcriptional level were detected using qPCR. ( E ) SP1 expression at the protein level was detected by Western blot. All experiments were performed in at least triplicate. Statistical significance was determined by one-way ANOVA with Tukey’s post hoc test. ns: not significant, * P < 0.05, ** P < 0.01, *** P < 0.001

    Journal: Cellular and Molecular Life Sciences: CMLS

    Article Title: Inflammation-induced LncRNA SNHG1 orchestrates spermatogonium development in non-obstructive azoospermia via IL-17 A signaling pathway

    doi: 10.1007/s00018-025-06055-3

    Figure Lengend Snippet: SP1 knockdown reduces the LPS-induced spermatogonia dysfunction. ( A ) Cell proliferation was detected using EdU staining. ( B - C ) Cell apoptosis was detected using flow cytometry and the TUNEL assay. ( D ) Expression levels of SNHG1 and SP1 at the transcriptional level were detected using qPCR. ( E ) SP1 expression at the protein level was detected by Western blot. All experiments were performed in at least triplicate. Statistical significance was determined by one-way ANOVA with Tukey’s post hoc test. ns: not significant, * P < 0.05, ** P < 0.01, *** P < 0.001

    Article Snippet: For cell lines, the one-step TUNEL apoptosis assay kit with Cy3 (Beyotime, China) was used according to the manufacturer’s instructions.

    Techniques: Knockdown, Staining, Flow Cytometry, TUNEL Assay, Expressing, Western Blot

    SNHG1 knockdown reduces LPS-induced spermatogonial dysfunction. ( A ) Cell proliferation was detected by EdU staining. ( B - C ) Cell apoptosis was detected by flow cytometry and TUNEL assay. ( D ) Expression levels of SNHG1 and SP1 at the transcriptional level were detected by qPCR. ( E ) SP1 expression at the protein level was detected by Western blot. ( F – H ) IF analysis of SP1 , C-kit, and Oct4 expression. All experiments were performed in at least triplicate. Statistical significance was determined by one-way ANOVA with Tukey’s post hoc test. ns: not significant, * P < 0.05, ** P < 0.01, *** P < 0.001

    Journal: Cellular and Molecular Life Sciences: CMLS

    Article Title: Inflammation-induced LncRNA SNHG1 orchestrates spermatogonium development in non-obstructive azoospermia via IL-17 A signaling pathway

    doi: 10.1007/s00018-025-06055-3

    Figure Lengend Snippet: SNHG1 knockdown reduces LPS-induced spermatogonial dysfunction. ( A ) Cell proliferation was detected by EdU staining. ( B - C ) Cell apoptosis was detected by flow cytometry and TUNEL assay. ( D ) Expression levels of SNHG1 and SP1 at the transcriptional level were detected by qPCR. ( E ) SP1 expression at the protein level was detected by Western blot. ( F – H ) IF analysis of SP1 , C-kit, and Oct4 expression. All experiments were performed in at least triplicate. Statistical significance was determined by one-way ANOVA with Tukey’s post hoc test. ns: not significant, * P < 0.05, ** P < 0.01, *** P < 0.001

    Article Snippet: For cell lines, the one-step TUNEL apoptosis assay kit with Cy3 (Beyotime, China) was used according to the manufacturer’s instructions.

    Techniques: Knockdown, Staining, Flow Cytometry, TUNEL Assay, Expressing, Western Blot

    IL-17A signaling pathway blockade rescued the SNHG1 -induced cell dysfunction. ( A ) Cell proliferation was detected using EdU staining. ( B - C ) Cell apoptosis detected by flow cytometry and TUNEL assay. ( D ) Expression levels of SNHG1 and SP1 at the transcriptional level were detected by qPCR. ( E ) SP1 expression at the protein level was detected using a Western blot. ( F – H ) IF analysis of SP1 , C-kit, and Oct4 expression. All experiments were performed in at least triplicate. Statistical significance was determined by one-way ANOVA with Tukey’s post hoc test. ns: not significant, ** P < 0.01, *** P < 0.001

    Journal: Cellular and Molecular Life Sciences: CMLS

    Article Title: Inflammation-induced LncRNA SNHG1 orchestrates spermatogonium development in non-obstructive azoospermia via IL-17 A signaling pathway

    doi: 10.1007/s00018-025-06055-3

    Figure Lengend Snippet: IL-17A signaling pathway blockade rescued the SNHG1 -induced cell dysfunction. ( A ) Cell proliferation was detected using EdU staining. ( B - C ) Cell apoptosis detected by flow cytometry and TUNEL assay. ( D ) Expression levels of SNHG1 and SP1 at the transcriptional level were detected by qPCR. ( E ) SP1 expression at the protein level was detected using a Western blot. ( F – H ) IF analysis of SP1 , C-kit, and Oct4 expression. All experiments were performed in at least triplicate. Statistical significance was determined by one-way ANOVA with Tukey’s post hoc test. ns: not significant, ** P < 0.01, *** P < 0.001

    Article Snippet: For cell lines, the one-step TUNEL apoptosis assay kit with Cy3 (Beyotime, China) was used according to the manufacturer’s instructions.

    Techniques: Staining, Flow Cytometry, TUNEL Assay, Expressing, Western Blot

    Re-expressing SNHGI in SP1-knock-down cells protect cells from inflammatory damage. ( A - C ) Expression levels of SP1 , SNHG1 , and IL-17 A were detected by QPCR assay. ( D ) The WB method was employed to assess the protein expression levels of SP1 and IL-17 A . ( E ) EdU staining was utilized to evaluate cell proliferation. ( F ) Flow cytometry was applied to detect cell apoptosis. All experiments were performed in at least triplicate. Statistical significance was determined by one-way ANOVA with Tukey’s post hoc test. ns: not significant, ** P < 0.01, *** P < 0.001

    Journal: Cellular and Molecular Life Sciences: CMLS

    Article Title: Inflammation-induced LncRNA SNHG1 orchestrates spermatogonium development in non-obstructive azoospermia via IL-17 A signaling pathway

    doi: 10.1007/s00018-025-06055-3

    Figure Lengend Snippet: Re-expressing SNHGI in SP1-knock-down cells protect cells from inflammatory damage. ( A - C ) Expression levels of SP1 , SNHG1 , and IL-17 A were detected by QPCR assay. ( D ) The WB method was employed to assess the protein expression levels of SP1 and IL-17 A . ( E ) EdU staining was utilized to evaluate cell proliferation. ( F ) Flow cytometry was applied to detect cell apoptosis. All experiments were performed in at least triplicate. Statistical significance was determined by one-way ANOVA with Tukey’s post hoc test. ns: not significant, ** P < 0.01, *** P < 0.001

    Article Snippet: For cell lines, the one-step TUNEL apoptosis assay kit with Cy3 (Beyotime, China) was used according to the manufacturer’s instructions.

    Techniques: Expressing, Knockdown, Staining, Flow Cytometry