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Structured Review

Shanghai Shenggong Co goat serum blocking solution
Goat Serum Blocking Solution, supplied by Shanghai Shenggong Co, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Related Articles

Immunostaining:

Article Title: Study of the antioxidant capacity of astaxanthin in cells against radiation-induced strong oxidative stress
Article Snippet: Astaxanthin, an oxygen-containing carotenoid derived from Haematococcus pluvialis, has excellent antioxidant properties and great potential in antioxidant, immunomodulation, anti-cancer, skin protection and aquaculture.. However, the protective effect of astaxanthin on cells under the strong oxidative stress caused by external factors such as ionizing radiation has not been investigated.. For this purpose, we employed γ-ray, one type of strong energy-penetrating radiations, to irradiate the normal cells, namely, BHK-21 and CHOK1 cells, and studied the antioxidant capacity, or, the protective effect of astaxanthin in the cells.

Blocking Assay:

Article Title: Study of the antioxidant capacity of astaxanthin in cells against radiation-induced strong oxidative stress
Article Snippet: Astaxanthin, an oxygen-containing carotenoid derived from Haematococcus pluvialis, has excellent antioxidant properties and great potential in antioxidant, immunomodulation, anti-cancer, skin protection and aquaculture.. However, the protective effect of astaxanthin on cells under the strong oxidative stress caused by external factors such as ionizing radiation has not been investigated.. For this purpose, we employed γ-ray, one type of strong energy-penetrating radiations, to irradiate the normal cells, namely, BHK-21 and CHOK1 cells, and studied the antioxidant capacity, or, the protective effect of astaxanthin in the cells.

Article Title: Modulating gut microbiota to enhance anti-PD-1/PD-L1 immunotherapy in hepatocellular carcinoma: the role of Lactobacillus kefiranofaciens and SOCS3 regulation.
Article Snippet: .. After treatment with 3% H2O2 at room temperature to inactivate endogenous peroxidases, sections were incubated with normal goat serum blocking solution (E510009, Shanghai Shenggong Biological Engineering Co., China) at room temperature. .. After incubation was completed, the specific primary antibodies against SOCS3, JAK2, STAT3, Interferon Regulatory Factor 1 (IRF1), and Programmed Death-Ligand 1 (PD-L1) (catalog numbers: ab280884, PA5120123, ab68153, PA5-50512, and MA5-32450; dilutions: 1:1000, 1:100, 1:200, 1:100, and 1:100, respectively; procured from Abcam, UK, or Thermo Fisher, USA) were applied and incubated overnight at 4 °C.

Staining:

Article Title: Study of the antioxidant capacity of astaxanthin in cells against radiation-induced strong oxidative stress
Article Snippet: Astaxanthin, an oxygen-containing carotenoid derived from Haematococcus pluvialis, has excellent antioxidant properties and great potential in antioxidant, immunomodulation, anti-cancer, skin protection and aquaculture.. However, the protective effect of astaxanthin on cells under the strong oxidative stress caused by external factors such as ionizing radiation has not been investigated.. For this purpose, we employed γ-ray, one type of strong energy-penetrating radiations, to irradiate the normal cells, namely, BHK-21 and CHOK1 cells, and studied the antioxidant capacity, or, the protective effect of astaxanthin in the cells.

Cell Culture:

Article Title: Study of the antioxidant capacity of astaxanthin in cells against radiation-induced strong oxidative stress
Article Snippet: Astaxanthin, an oxygen-containing carotenoid derived from Haematococcus pluvialis, has excellent antioxidant properties and great potential in antioxidant, immunomodulation, anti-cancer, skin protection and aquaculture.. However, the protective effect of astaxanthin on cells under the strong oxidative stress caused by external factors such as ionizing radiation has not been investigated.. For this purpose, we employed γ-ray, one type of strong energy-penetrating radiations, to irradiate the normal cells, namely, BHK-21 and CHOK1 cells, and studied the antioxidant capacity, or, the protective effect of astaxanthin in the cells.

Membrane:

Article Title: Study of the antioxidant capacity of astaxanthin in cells against radiation-induced strong oxidative stress
Article Snippet: Astaxanthin, an oxygen-containing carotenoid derived from Haematococcus pluvialis, has excellent antioxidant properties and great potential in antioxidant, immunomodulation, anti-cancer, skin protection and aquaculture.. However, the protective effect of astaxanthin on cells under the strong oxidative stress caused by external factors such as ionizing radiation has not been investigated.. For this purpose, we employed γ-ray, one type of strong energy-penetrating radiations, to irradiate the normal cells, namely, BHK-21 and CHOK1 cells, and studied the antioxidant capacity, or, the protective effect of astaxanthin in the cells.

Protease Inhibitor:

Article Title: Study of the antioxidant capacity of astaxanthin in cells against radiation-induced strong oxidative stress
Article Snippet: Astaxanthin, an oxygen-containing carotenoid derived from Haematococcus pluvialis, has excellent antioxidant properties and great potential in antioxidant, immunomodulation, anti-cancer, skin protection and aquaculture.. However, the protective effect of astaxanthin on cells under the strong oxidative stress caused by external factors such as ionizing radiation has not been investigated.. For this purpose, we employed γ-ray, one type of strong energy-penetrating radiations, to irradiate the normal cells, namely, BHK-21 and CHOK1 cells, and studied the antioxidant capacity, or, the protective effect of astaxanthin in the cells.

Incubation:

Article Title: Modulating gut microbiota to enhance anti-PD-1/PD-L1 immunotherapy in hepatocellular carcinoma: the role of Lactobacillus kefiranofaciens and SOCS3 regulation.
Article Snippet: .. After treatment with 3% H2O2 at room temperature to inactivate endogenous peroxidases, sections were incubated with normal goat serum blocking solution (E510009, Shanghai Shenggong Biological Engineering Co., China) at room temperature. .. After incubation was completed, the specific primary antibodies against SOCS3, JAK2, STAT3, Interferon Regulatory Factor 1 (IRF1), and Programmed Death-Ligand 1 (PD-L1) (catalog numbers: ab280884, PA5120123, ab68153, PA5-50512, and MA5-32450; dilutions: 1:1000, 1:100, 1:200, 1:100, and 1:100, respectively; procured from Abcam, UK, or Thermo Fisher, USA) were applied and incubated overnight at 4 °C.



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The N- and C-termini dependency for TCTN1 in the transition zone localization (A) <t>Immunostaining</t> images showing the ciliary base signals using HA antibody (green) in WT, tctn1 , TCTN1, DUF1619, ΔDUF1619, N-DUF1619, and DUF1619-C cell lines. The signal of acetylated α-tubulin (Ac-tubulin, red) marks the cilium. The white arrowheads mark the ciliary base (ciliary transition zone). The insets show higher magnification views of the transition zone puncta. The statistical analysis of the percentage of fluorescence localization at the TZ is also presented ( n = 17, 19, 25, 35, 26, 41, and 41). Scale bars, 5 μm.
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The N- and C-termini dependency for TCTN1 in the transition zone localization (A) <t>Immunostaining</t> images showing the ciliary base signals using HA antibody (green) in WT, tctn1 , TCTN1, DUF1619, ΔDUF1619, N-DUF1619, and DUF1619-C cell lines. The signal of acetylated α-tubulin (Ac-tubulin, red) marks the cilium. The white arrowheads mark the ciliary base (ciliary transition zone). The insets show higher magnification views of the transition zone puncta. The statistical analysis of the percentage of fluorescence localization at the TZ is also presented ( n = 17, 19, 25, 35, 26, 41, and 41). Scale bars, 5 μm.
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The impact of Tet2 knockdown on DPA@NM@CTZE expression. ( A-B ) It shows <t>IHC</t> images of LC3B, OCN, and RUNX2. Scale bar: 400 μm. (C-D ) It displays calcein double-standard images and analysis. Scale bar: 100 μm. Results are expressed as Mean ± SD, with significance denoted by ∗P < 0.05, ∗∗P < 0.01, and ∗∗∗P < 0.001, n = 5.
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The impact of Tet2 knockdown on DPA@NM@CTZE expression. ( A-B ) It shows <t>IHC</t> images of LC3B, OCN, and RUNX2. Scale bar: 400 μm. (C-D ) It displays calcein double-standard images and analysis. Scale bar: 100 μm. Results are expressed as Mean ± SD, with significance denoted by ∗P < 0.05, ∗∗P < 0.01, and ∗∗∗P < 0.001, n = 5.
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The impact of Tet2 knockdown on DPA@NM@CTZE expression. ( A-B ) It shows <t>IHC</t> images of LC3B, OCN, and RUNX2. Scale bar: 400 μm. (C-D ) It displays calcein double-standard images and analysis. Scale bar: 100 μm. Results are expressed as Mean ± SD, with significance denoted by ∗P < 0.05, ∗∗P < 0.01, and ∗∗∗P < 0.001, n = 5.
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The impact of Tet2 knockdown on DPA@NM@CTZE expression. ( A-B ) It shows <t>IHC</t> images of LC3B, OCN, and RUNX2. Scale bar: 400 μm. (C-D ) It displays calcein double-standard images and analysis. Scale bar: 100 μm. Results are expressed as Mean ± SD, with significance denoted by ∗P < 0.05, ∗∗P < 0.01, and ∗∗∗P < 0.001, n = 5.
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The impact of Tet2 knockdown on DPA@NM@CTZE expression. ( A-B ) It shows <t>IHC</t> images of LC3B, OCN, and RUNX2. Scale bar: 400 μm. (C-D ) It displays calcein double-standard images and analysis. Scale bar: 100 μm. Results are expressed as Mean ± SD, with significance denoted by ∗P < 0.05, ∗∗P < 0.01, and ∗∗∗P < 0.001, n = 5.
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The impact of Tet2 knockdown on DPA@NM@CTZE expression. ( A-B ) It shows <t>IHC</t> images of LC3B, OCN, and RUNX2. Scale bar: 400 μm. (C-D ) It displays calcein double-standard images and analysis. Scale bar: 100 μm. Results are expressed as Mean ± SD, with significance denoted by ∗P < 0.05, ∗∗P < 0.01, and ∗∗∗P < 0.001, n = 5.
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Image Search Results


The N- and C-termini dependency for TCTN1 in the transition zone localization (A) Immunostaining images showing the ciliary base signals using HA antibody (green) in WT, tctn1 , TCTN1, DUF1619, ΔDUF1619, N-DUF1619, and DUF1619-C cell lines. The signal of acetylated α-tubulin (Ac-tubulin, red) marks the cilium. The white arrowheads mark the ciliary base (ciliary transition zone). The insets show higher magnification views of the transition zone puncta. The statistical analysis of the percentage of fluorescence localization at the TZ is also presented ( n = 17, 19, 25, 35, 26, 41, and 41). Scale bars, 5 μm.

Journal: iScience

Article Title: Profiling truncated variants of TCTN1 unveils the essential role of its integrity for ciliogenesis

doi: 10.1016/j.isci.2025.114190

Figure Lengend Snippet: The N- and C-termini dependency for TCTN1 in the transition zone localization (A) Immunostaining images showing the ciliary base signals using HA antibody (green) in WT, tctn1 , TCTN1, DUF1619, ΔDUF1619, N-DUF1619, and DUF1619-C cell lines. The signal of acetylated α-tubulin (Ac-tubulin, red) marks the cilium. The white arrowheads mark the ciliary base (ciliary transition zone). The insets show higher magnification views of the transition zone puncta. The statistical analysis of the percentage of fluorescence localization at the TZ is also presented ( n = 17, 19, 25, 35, 26, 41, and 41). Scale bars, 5 μm.

Article Snippet: Immunostaining Blocking/Primary Antibody Dilution Solution , Sangon Biotech , Cat#E674004.

Techniques: Immunostaining, Fluorescence

The transition zone localizations of NPHP4 or NPHP8 in truncated TCTN1 mutants are not altered (A and B) Immunostaining images displaying the ciliary base puncta of NPHP4 (A) or NPHP8 (B) in WT, tctn1 ::TCTN1-HA (TCTN1), and tctn1 ::TCTN1(DUF1619)-HA (DUF1619) cells. All the cells were immunostained with anti-NPHP4 (green) or anti-NPHP8 (green) and anti-acetylated α-tubulin (Ac-tubulin, red) antibodies. The nuclei were stained with DAPI (blue). The white arrowheads indicate the ciliary base (ciliary transition zone). The insets show higher magnification views of the transition zone region. The brightfield (BF) and merge channels are also showed. Scale bars, 5 μm. See also for other truncated strains.

Journal: iScience

Article Title: Profiling truncated variants of TCTN1 unveils the essential role of its integrity for ciliogenesis

doi: 10.1016/j.isci.2025.114190

Figure Lengend Snippet: The transition zone localizations of NPHP4 or NPHP8 in truncated TCTN1 mutants are not altered (A and B) Immunostaining images displaying the ciliary base puncta of NPHP4 (A) or NPHP8 (B) in WT, tctn1 ::TCTN1-HA (TCTN1), and tctn1 ::TCTN1(DUF1619)-HA (DUF1619) cells. All the cells were immunostained with anti-NPHP4 (green) or anti-NPHP8 (green) and anti-acetylated α-tubulin (Ac-tubulin, red) antibodies. The nuclei were stained with DAPI (blue). The white arrowheads indicate the ciliary base (ciliary transition zone). The insets show higher magnification views of the transition zone region. The brightfield (BF) and merge channels are also showed. Scale bars, 5 μm. See also for other truncated strains.

Article Snippet: Immunostaining Blocking/Primary Antibody Dilution Solution , Sangon Biotech , Cat#E674004.

Techniques: Immunostaining, Staining

The impact of Tet2 knockdown on DPA@NM@CTZE expression. ( A-B ) It shows IHC images of LC3B, OCN, and RUNX2. Scale bar: 400 μm. (C-D ) It displays calcein double-standard images and analysis. Scale bar: 100 μm. Results are expressed as Mean ± SD, with significance denoted by ∗P < 0.05, ∗∗P < 0.01, and ∗∗∗P < 0.001, n = 5.

Journal: Materials Today Bio

Article Title: A biomimetic multimodal nanoplatform combining neutrophil-coated two-dimensional metalloporphyrinic framework nanosheet and exendin-4 to treat obesity-related osteoporosis

doi: 10.1016/j.mtbio.2025.102009

Figure Lengend Snippet: The impact of Tet2 knockdown on DPA@NM@CTZE expression. ( A-B ) It shows IHC images of LC3B, OCN, and RUNX2. Scale bar: 400 μm. (C-D ) It displays calcein double-standard images and analysis. Scale bar: 100 μm. Results are expressed as Mean ± SD, with significance denoted by ∗P < 0.05, ∗∗P < 0.01, and ∗∗∗P < 0.001, n = 5.

Article Snippet: Subsequently, 1 mL of pre-cooled methanol was added, and the samples were placed in a −20 °C refrigerator for 10 min. After this step, the samples were washed 3 times with pre-cooled PBS, each wash lasting 5 min. Triton X-100 (1 mL) was then added for 10 min, and the samples were incubated with an Immunostaining blocking solution (Beyotime, China).

Techniques: Knockdown, Expressing