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bcl2 associated x apoptosis regulator  (Proteintech)


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    Proteintech bcl2 associated x apoptosis regulator
    Bcl2 Associated X Apoptosis Regulator, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 4672 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/bcl2+associated+x/BCL2+Antibody/10__1161_slash_jaha__125__043108-83-20-25
    Average 96 stars, based on 4672 article reviews
    bcl2 associated x apoptosis regulator - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Recombinant:

    Article Title: Untargeted serum and gastric metabolomics and network pharmacology analysis reveal the superior efficacy of zingiberis rhizoma recens-/euodiae fructus-processed Coptidis Rhizoma on gastric ulcer rats.
    Article Snippet: Ethnopharmacological relevance: Zingiberis rhizoma recens-/wine-/euodiae fructus-processed Coptidis Rhizoma (CR, zCR/wCR/eCR) are the commonly used processed products of CR in clinic.. After being processed with different excipients, the efficacy of CR will change accordingly.. I.e., wCR could resolve excessive heat of the upper energizer, zCR could eliminate gastric heat and harmonize the stomach, eCR could smooth the liver and harmonize the stomach.

    Incubation:

    Article Title: Bacillus subtilis alleviates excessive apoptosis of intestinal epithelial cells in intrauterine growth restriction suckling piglets via the members of Bcl-2 and caspase families.
    Article Snippet: BACKGROUND: The intestine is a barrier resisting various stress responses.. Intrauterine growth restriction (IUGR) can cause the damage of intestinal barrier via destroying the balance of intestinal epithelial cells' proliferation and apoptosis.. Bacillus subtilis has been reported to regulate intestinal epithelial cells' proliferation and apoptosis.

    Article Title: Albiflorin enhances the antitumor effects of propofol in hepatocellular carcinoma cells by inhibiting the Wnt/β-catenin signaling activation
    Article Snippet: Equal amounts of protein (20 μg) were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and transferred onto polyvinylidene fluoride (PVDF) membranes (Millipore, USA). .. The membranes were blocked with 5% non-fat milk for 1 h at room temperature and then incubated overnight at 4 °C with primary antibodies, including B-cell lymphoma-2 (Bcl-2, 12789-1-AP, 1:2,000, Proteintech), Bcl2-associated X (Bax, 50599-2-Ig, 1:2,000, Proteintech), Wnt3a (26744-1-AP, 1:2,000, Proteintech), β-catenin (51067-2-AP, 1:5,000, Proteintech), E-cadherin (14472, 1:1,000, CST), N-cadherin (14215, 1:1,000, CST), cyclin D1 (60186-1-Ig, 1:5,000, Proteintech), c-Myc (13987T, 1:2,000, CST), and GAPDH (60004-1-Ig, 1:50,000, Proteintech). .. The following day, membranes were washed three times with Tris-Borate-Sodium Tween-20 (TBST) and incubated with HRP-conjugated secondary antibodies (7076/7074, 1:1,000, CST) for 1 h at room temperature.



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    APS modulates apoptotic protein expressions in BMSCs exposed to ATO. Cells were exposed to 0.5 μmol/L ATO, and 0.5 μmol/L ATO + APS (20, 40, 100, and 200 μg/mL) for 48 h. (A) Western blotting analysis was applied to detect protein expression of p16, p53, cleaved Caspase-3, <t>Caspase-3,</t> <t>Bcl-2</t> and Bax, β -actin was used as a loading control, n = 3. (B) Western blotting analysis was used to detect protein expression of p-Akt and Akt, β -actin was served as a loading control, n = 3. A two-tailed Student’s t -test was used to compare differences between two experimental groups. Error bars represent mean ± SEM. * P < 0.05, ** P < 0.01, *** P < 0.001 vs control group, # P < 0.05, ## P < 0.01 vs ATO group.
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    APS modulates apoptotic protein expressions in BMSCs exposed to ATO. Cells were exposed to 0.5 μmol/L ATO, and 0.5 μmol/L ATO + APS (20, 40, 100, and 200 μg/mL) for 48 h. (A) Western blotting analysis was applied to detect protein expression of p16, p53, cleaved Caspase-3, <t>Caspase-3,</t> <t>Bcl-2</t> and Bax, β -actin was used as a loading control, n = 3. (B) Western blotting analysis was used to detect protein expression of p-Akt and Akt, β -actin was served as a loading control, n = 3. A two-tailed Student’s t -test was used to compare differences between two experimental groups. Error bars represent mean ± SEM. * P < 0.05, ** P < 0.01, *** P < 0.001 vs control group, # P < 0.05, ## P < 0.01 vs ATO group.
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    APS modulates apoptotic protein expressions in BMSCs exposed to ATO. Cells were exposed to 0.5 μmol/L ATO, and 0.5 μmol/L ATO + APS (20, 40, 100, and 200 μg/mL) for 48 h. (A) Western blotting analysis was applied to detect protein expression of p16, p53, cleaved Caspase-3, Caspase-3, Bcl-2 and Bax, β -actin was used as a loading control, n = 3. (B) Western blotting analysis was used to detect protein expression of p-Akt and Akt, β -actin was served as a loading control, n = 3. A two-tailed Student’s t -test was used to compare differences between two experimental groups. Error bars represent mean ± SEM. * P < 0.05, ** P < 0.01, *** P < 0.001 vs control group, # P < 0.05, ## P < 0.01 vs ATO group.

    Journal: Chinese Herbal Medicines

    Article Title: Astragalus polysaccharides inhibit arsenic trioxide-induced BMSCs damage through inhibition of Jnk and p38 signaling pathways

    doi: 10.1016/j.chmed.2025.03.007

    Figure Lengend Snippet: APS modulates apoptotic protein expressions in BMSCs exposed to ATO. Cells were exposed to 0.5 μmol/L ATO, and 0.5 μmol/L ATO + APS (20, 40, 100, and 200 μg/mL) for 48 h. (A) Western blotting analysis was applied to detect protein expression of p16, p53, cleaved Caspase-3, Caspase-3, Bcl-2 and Bax, β -actin was used as a loading control, n = 3. (B) Western blotting analysis was used to detect protein expression of p-Akt and Akt, β -actin was served as a loading control, n = 3. A two-tailed Student’s t -test was used to compare differences between two experimental groups. Error bars represent mean ± SEM. * P < 0.05, ** P < 0.01, *** P < 0.001 vs control group, # P < 0.05, ## P < 0.01 vs ATO group.

    Article Snippet: The membranes were then incubated with primary antibodies against B-cell lymphoma 2 (Bcl-2) (1:1 000, Proteintech, Chicago, USA, Cat. No. 68103-1-lg), Bcl-2-associated X protein (Bax) (1:1 000, Proteintech, Chicago, USA, Cat. No. 50599-2-lg), Caspase-3 (1:1 000, Proteintech, Chicago, USA, Cat. No. 19677-1-AP), cleaved Caspase-3 (1:2 000, Proteintech, Chicago, USA, Cat. No. 68773-1-lg), protein kinase B (Akt) (1:1 000, Cell signaling, Boston, USA, Cat. No. 9272) and phosphorylated-Akt (1:1 000, Cell signaling, Boston, USA, Cat. No. 4060), p53 (1:500, Gene Tex, California, USA, Cat. No. GTX70214), p16 (1:1 000, Proteintech, Chicago, USA, Cat. No.10883-1-AP), p38 mitogen-activated protein kinase (MAPK) (1:1 000, Proteintech, Chicago, USA, Cat. No.14064-1-AP), phosphorylated-p38 MAPK (1:1 000, Proteintech, Chicago, USA, Cat. No. 28796-1-AP), extracellular signal-regulated kinase (Erk) (1:2 000, Abcam, Cambridge, UK, Cat. No. ab184699), phosphorylated-Erk (1:2 000, Abcam, Cambridge, UK, Cat. No. ab201015), c-Jun N -terminal kinase (Jnk) (1:1 000, Proteintech, Chicago, USA, Cat. No.66210-1-lG), phosphorylated-Jnk (1:2 000, Abcam, Cambridge, UK, Cat. No. ab278538), GTPase-activating protein (Gap) (1:1 000, Abcam, Cambridge, UK, Cat. No. ab8245), and β -actin (1:1 000, Abcam, Cambridge, UK, Cat. No. ab8226) at 4 °C overnight.

    Techniques: Western Blot, Expressing, Control, Two Tailed Test