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Structured Review

Bethyl a304 512a
A304 512a, supplied by Bethyl, used in various techniques. Bioz Stars score: 93/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/a304+512a/Syntaxin+7+Antibody/pmc11728075-325-20-18
Average 93 stars, based on 14 article reviews
a304 512a - by Bioz Stars, 2026-10
93/100 stars

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Related Articles

Immunostaining:

Article Title: Identification of the role of SNARE proteins in rAAV vector production through interaction with the viral MAAP
Article Snippet: An anti-GST (#AE001) and an anti-β-actin (#AC026) were purchased from AbClonal (Woburn, MA). .. An anti-V5 (#R960-25) was purchased from Invitrogen (Carlsbad, CA), and anti-STX7 antibodies were purchased from AbClonal (#A8057) and Bethyl Laboratories (#A304-512A; Montgomery, TX) for immunostaining and immunoblotting, respectively. .. An anti-SNAP23 (#10825-1-AP) was purchased from Proteintech (Rosemont, IL).

Article Title: Identification of the role of SNARE proteins in rAAV vector production through interaction with the viral membrane-associated accessory protein (MAAP)
Article Snippet: An anti-GST (#AE001) and an anti-β-actin (#AC026) 577 were purchased from AbClonal (Woburn, MA). .. An anti-V5 (# R960-25) was purchased from 578 Invitrogen (Carlsbad, CA), and anti-STX7 antibodies were purchased from AbClonal (#A8057) 579 and Bethyl Laboratories (#A304-512A; Montgomery, TX) for immunostaining and 580 immunoblotting, respectively. .. An anti-SNAP23 (#10825-1-AP) was purchased from Proteintech 581 (Rosemont, IL).

Western Blot:

Article Title: Identification of the role of SNARE proteins in rAAV vector production through interaction with the viral MAAP
Article Snippet: An anti-GST (#AE001) and an anti-β-actin (#AC026) were purchased from AbClonal (Woburn, MA). .. An anti-V5 (#R960-25) was purchased from Invitrogen (Carlsbad, CA), and anti-STX7 antibodies were purchased from AbClonal (#A8057) and Bethyl Laboratories (#A304-512A; Montgomery, TX) for immunostaining and immunoblotting, respectively. .. An anti-SNAP23 (#10825-1-AP) was purchased from Proteintech (Rosemont, IL).

Article Title: Identification of the role of SNARE proteins in rAAV vector production through interaction with the viral membrane-associated accessory protein (MAAP)
Article Snippet: An anti-GST (#AE001) and an anti-β-actin (#AC026) 577 were purchased from AbClonal (Woburn, MA). .. An anti-V5 (# R960-25) was purchased from 578 Invitrogen (Carlsbad, CA), and anti-STX7 antibodies were purchased from AbClonal (#A8057) 579 and Bethyl Laboratories (#A304-512A; Montgomery, TX) for immunostaining and 580 immunoblotting, respectively. .. An anti-SNAP23 (#10825-1-AP) was purchased from Proteintech 581 (Rosemont, IL).



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Bethyl a304 512a
A304 512a, supplied by Bethyl, 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/a304+512a/Syntaxin+7+Antibody/pmc11728075-325-20-18
Average 93 stars, based on 1 article reviews
a304 512a - by Bioz Stars, 2026-10
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Figure 4. DEP impair autophagic flux in the degradation stage. (a) HUVECs infected with RFP-LC3B-GFP- expressing adenovirus were exposed to DEP (70 µg/ml) for 18 h and autolysosome formation was examined under fluorescence microscopy. (b) The number of yellow signals per cell was counted from 10 randomly selected cells. Statistical analysis was performed using two-tailed Student’s t test. **P < 0.02 versus control. (c) HUVECs were pre-incubated with Bafilomysin A1 (Baf A1, 100 nM) for 3 h and exposed to DEP (70 μg/ ml) for an additional 12 h. LC3B level was measured by immunoblotting. (d) Quantification of LC3BII levels normalized to β-actin. Results are presented as means ± SD (n = 3). Statistical analysis was performed using one-way ANOVA. **P < 0.02 versus no treatment. (e) HUVECs were exposed to DEP (70 μg/ml) for 24 h and protein levels of STX17, VAMP8, SNAP29, YKT6, <t>STX7,</t> and β-actin were measured by immunoblotting. (f) Quantification of STX17, VAMP8, SNAP29, YKT6, and STX7 levels normalized to β-actin. Results are presented as means ± SD (n = 3). Statistical analysis was performed using two-tailed Student’s t test. **P < 0.02 versus control.
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Figure 4. DEP impair autophagic flux in the degradation stage. (a) HUVECs infected with RFP-LC3B-GFP- expressing adenovirus were exposed to DEP (70 µg/ml) for 18 h and autolysosome formation was examined under fluorescence microscopy. (b) The number of yellow signals per cell was counted from 10 randomly selected cells. Statistical analysis was performed using two-tailed Student’s t test. **P < 0.02 versus control. (c) HUVECs were pre-incubated with Bafilomysin A1 (Baf A1, 100 nM) for 3 h and exposed to DEP (70 μg/ ml) for an additional 12 h. LC3B level was measured by immunoblotting. (d) Quantification of LC3BII levels normalized to β-actin. Results are presented as means ± SD (n = 3). Statistical analysis was performed using one-way ANOVA. **P < 0.02 versus no treatment. (e) HUVECs were exposed to DEP (70 μg/ml) for 24 h and protein levels of STX17, VAMP8, SNAP29, YKT6, <t>STX7,</t> and β-actin were measured by immunoblotting. (f) Quantification of STX17, VAMP8, SNAP29, YKT6, and STX7 levels normalized to β-actin. Results are presented as means ± SD (n = 3). Statistical analysis was performed using two-tailed Student’s t test. **P < 0.02 versus control.
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Figure 4. DEP impair autophagic flux in the degradation stage. (a) HUVECs infected with RFP-LC3B-GFP- expressing adenovirus were exposed to DEP (70 µg/ml) for 18 h and autolysosome formation was examined under fluorescence microscopy. (b) The number of yellow signals per cell was counted from 10 randomly selected cells. Statistical analysis was performed using two-tailed Student’s t test. **P < 0.02 versus control. (c) HUVECs were pre-incubated with Bafilomysin A1 (Baf A1, 100 nM) for 3 h and exposed to DEP (70 μg/ ml) for an additional 12 h. LC3B level was measured by immunoblotting. (d) Quantification of LC3BII levels normalized to β-actin. Results are presented as means ± SD (n = 3). Statistical analysis was performed using one-way ANOVA. **P < 0.02 versus no treatment. (e) HUVECs were exposed to DEP (70 μg/ml) for 24 h and protein levels of STX17, VAMP8, SNAP29, YKT6, <t>STX7,</t> and β-actin were measured by immunoblotting. (f) Quantification of STX17, VAMP8, SNAP29, YKT6, and STX7 levels normalized to β-actin. Results are presented as means ± SD (n = 3). Statistical analysis was performed using two-tailed Student’s t test. **P < 0.02 versus control.
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Figure 4. DEP impair autophagic flux in the degradation stage. (a) HUVECs infected with RFP-LC3B-GFP- expressing adenovirus were exposed to DEP (70 µg/ml) for 18 h and autolysosome formation was examined under fluorescence microscopy. (b) The number of yellow signals per cell was counted from 10 randomly selected cells. Statistical analysis was performed using two-tailed Student’s t test. **P < 0.02 versus control. (c) HUVECs were pre-incubated with Bafilomysin A1 (Baf A1, 100 nM) for 3 h and exposed to DEP (70 μg/ ml) for an additional 12 h. LC3B level was measured by immunoblotting. (d) Quantification of LC3BII levels normalized to β-actin. Results are presented as means ± SD (n = 3). Statistical analysis was performed using one-way ANOVA. **P < 0.02 versus no treatment. (e) HUVECs were exposed to DEP (70 μg/ml) for 24 h and protein levels of STX17, VAMP8, SNAP29, YKT6, <t>STX7,</t> and β-actin were measured by immunoblotting. (f) Quantification of STX17, VAMP8, SNAP29, YKT6, and STX7 levels normalized to β-actin. Results are presented as means ± SD (n = 3). Statistical analysis was performed using two-tailed Student’s t test. **P < 0.02 versus control.
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Figure 4. DEP impair autophagic flux in the degradation stage. (a) HUVECs infected with RFP-LC3B-GFP- expressing adenovirus were exposed to DEP (70 µg/ml) for 18 h and autolysosome formation was examined under fluorescence microscopy. (b) The number of yellow signals per cell was counted from 10 randomly selected cells. Statistical analysis was performed using two-tailed Student’s t test. **P < 0.02 versus control. (c) HUVECs were pre-incubated with Bafilomysin A1 (Baf A1, 100 nM) for 3 h and exposed to DEP (70 μg/ ml) for an additional 12 h. LC3B level was measured by immunoblotting. (d) Quantification of LC3BII levels normalized to β-actin. Results are presented as means ± SD (n = 3). Statistical analysis was performed using one-way ANOVA. **P < 0.02 versus no treatment. (e) HUVECs were exposed to DEP (70 μg/ml) for 24 h and protein levels of STX17, VAMP8, SNAP29, YKT6, <t>STX7,</t> and β-actin were measured by immunoblotting. (f) Quantification of STX17, VAMP8, SNAP29, YKT6, and STX7 levels normalized to β-actin. Results are presented as means ± SD (n = 3). Statistical analysis was performed using two-tailed Student’s t test. **P < 0.02 versus control.
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Rabbit Polyclonal Anti Stx7, supplied by Bethyl, 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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Image Search Results


Figure 4. DEP impair autophagic flux in the degradation stage. (a) HUVECs infected with RFP-LC3B-GFP- expressing adenovirus were exposed to DEP (70 µg/ml) for 18 h and autolysosome formation was examined under fluorescence microscopy. (b) The number of yellow signals per cell was counted from 10 randomly selected cells. Statistical analysis was performed using two-tailed Student’s t test. **P < 0.02 versus control. (c) HUVECs were pre-incubated with Bafilomysin A1 (Baf A1, 100 nM) for 3 h and exposed to DEP (70 μg/ ml) for an additional 12 h. LC3B level was measured by immunoblotting. (d) Quantification of LC3BII levels normalized to β-actin. Results are presented as means ± SD (n = 3). Statistical analysis was performed using one-way ANOVA. **P < 0.02 versus no treatment. (e) HUVECs were exposed to DEP (70 μg/ml) for 24 h and protein levels of STX17, VAMP8, SNAP29, YKT6, STX7, and β-actin were measured by immunoblotting. (f) Quantification of STX17, VAMP8, SNAP29, YKT6, and STX7 levels normalized to β-actin. Results are presented as means ± SD (n = 3). Statistical analysis was performed using two-tailed Student’s t test. **P < 0.02 versus control.

Journal: Scientific reports

Article Title: Diesel exhaust particles induce human umbilical vein endothelial cells apoptosis by accumulation of autophagosomes and caspase-8 activation.

doi: 10.1038/s41598-022-21044-3

Figure Lengend Snippet: Figure 4. DEP impair autophagic flux in the degradation stage. (a) HUVECs infected with RFP-LC3B-GFP- expressing adenovirus were exposed to DEP (70 µg/ml) for 18 h and autolysosome formation was examined under fluorescence microscopy. (b) The number of yellow signals per cell was counted from 10 randomly selected cells. Statistical analysis was performed using two-tailed Student’s t test. **P < 0.02 versus control. (c) HUVECs were pre-incubated with Bafilomysin A1 (Baf A1, 100 nM) for 3 h and exposed to DEP (70 μg/ ml) for an additional 12 h. LC3B level was measured by immunoblotting. (d) Quantification of LC3BII levels normalized to β-actin. Results are presented as means ± SD (n = 3). Statistical analysis was performed using one-way ANOVA. **P < 0.02 versus no treatment. (e) HUVECs were exposed to DEP (70 μg/ml) for 24 h and protein levels of STX17, VAMP8, SNAP29, YKT6, STX7, and β-actin were measured by immunoblotting. (f) Quantification of STX17, VAMP8, SNAP29, YKT6, and STX7 levels normalized to β-actin. Results are presented as means ± SD (n = 3). Statistical analysis was performed using two-tailed Student’s t test. **P < 0.02 versus control.

Article Snippet: The STX7 antibody was purchased from Bethyl Laboratories Inc. (Montgomery, TX, USA).

Techniques: Infection, Expressing, Fluorescence, Microscopy, Two Tailed Test, Control, Incubation, Western Blot

Journal: iScience

Article Title: Persistent coxsackievirus B1 infection triggers extensive changes in the transcriptome of human pancreatic ductal cells

doi: 10.1016/j.isci.2021.103653

Figure Lengend Snippet:

Article Snippet: Rabbit polyclonal anti-STX7 , Bethyl , Cat#A304-512A; RRID: AB_2620706.

Techniques: Immunofluorescence, Virus, Control, Recombinant, Reverse Transcription, Gene Expression, Software, Transformation Assay