bcl w Search Results


anti bcl w  (Cell Signaling Technology Inc)
95
Cell Signaling Technology Inc anti bcl w
Anti Bcl W, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human bcl w  (R&D Systems)
93
R&D Systems human bcl w
Human Bcl W, 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
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bcl w dna  (OriGene)
90
OriGene bcl w dna
Bcl W Dna, supplied by OriGene, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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bcl w  (Santa Cruz Biotechnology)
90
Santa Cruz Biotechnology bcl w
Bcl W, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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bcl2 polyclonal antibody  (Proteintech)
93
Proteintech bcl2 polyclonal antibody
Bcl2 Polyclonal Antibody, supplied by Proteintech, 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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bcl w catalog 824 bw 050  (R&D Systems)
90
R&D Systems bcl w catalog 824 bw 050
Bcl W Catalog 824 Bw 050, supplied by R&D Systems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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bcl w specific sirna  (Santa Cruz Biotechnology)
92
Santa Cruz Biotechnology bcl w specific sirna
FIGURE 6. The effect of miR-122 on TNFa/CHX induced apoptosis in pterygium epithelial cells. Pterygium epithelial cells were transfected with the miR-122 inhibitor (100 nM) with or without Bcl-w <t>siRNA/</t> control siRNA (50 nM) as indicated followed by stimulation with TNFa (20 ng/mL) plus/CHX (25 lg/mL) for 4 hours. (A) Tumor necrosis factor a/CHX-induced apoptosis of pterygium epithelial cells was determined by TUNEL/DAPI staining. (B) The percentage of apoptotic cells was calculated and plotted. Values are mean 6 SD from three separate experiments. *P < 0.05 compared with the control; #P < 0.05 compared with the cells stimulated by only miR-122 inhibitor. (C) Caspase 3/7 activity in pterygium epithelial cells was determined with Caspase-Glo 3/7 assay kit (Promega). Values are mean 6 SD from three separate experiments. *P < 0.05, comparison between the two indicated groups; #P < 0.05, comparison between the two indicated groups.
Bcl W Specific Sirna, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human recombinant bcl 2 proteins  (R&D Systems)
91
R&D Systems human recombinant bcl 2 proteins
FIGURE 6. The effect of miR-122 on TNFa/CHX induced apoptosis in pterygium epithelial cells. Pterygium epithelial cells were transfected with the miR-122 inhibitor (100 nM) with or without Bcl-w <t>siRNA/</t> control siRNA (50 nM) as indicated followed by stimulation with TNFa (20 ng/mL) plus/CHX (25 lg/mL) for 4 hours. (A) Tumor necrosis factor a/CHX-induced apoptosis of pterygium epithelial cells was determined by TUNEL/DAPI staining. (B) The percentage of apoptotic cells was calculated and plotted. Values are mean 6 SD from three separate experiments. *P < 0.05 compared with the control; #P < 0.05 compared with the cells stimulated by only miR-122 inhibitor. (C) Caspase 3/7 activity in pterygium epithelial cells was determined with Caspase-Glo 3/7 assay kit (Promega). Values are mean 6 SD from three separate experiments. *P < 0.05, comparison between the two indicated groups; #P < 0.05, comparison between the two indicated groups.
Human Recombinant Bcl 2 Proteins, supplied by R&D Systems, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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western blotting human recombinant trail  (R&D Systems)
91
R&D Systems western blotting human recombinant trail
FIGURE 6. The effect of miR-122 on TNFa/CHX induced apoptosis in pterygium epithelial cells. Pterygium epithelial cells were transfected with the miR-122 inhibitor (100 nM) with or without Bcl-w <t>siRNA/</t> control siRNA (50 nM) as indicated followed by stimulation with TNFa (20 ng/mL) plus/CHX (25 lg/mL) for 4 hours. (A) Tumor necrosis factor a/CHX-induced apoptosis of pterygium epithelial cells was determined by TUNEL/DAPI staining. (B) The percentage of apoptotic cells was calculated and plotted. Values are mean 6 SD from three separate experiments. *P < 0.05 compared with the control; #P < 0.05 compared with the cells stimulated by only miR-122 inhibitor. (C) Caspase 3/7 activity in pterygium epithelial cells was determined with Caspase-Glo 3/7 assay kit (Promega). Values are mean 6 SD from three separate experiments. *P < 0.05, comparison between the two indicated groups; #P < 0.05, comparison between the two indicated groups.
Western Blotting Human Recombinant Trail, supplied by R&D Systems, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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af8241 bcl xl wb n a rabbit  (R&D Systems)
91
R&D Systems af8241 bcl xl wb n a rabbit
FIGURE 6. The effect of miR-122 on TNFa/CHX induced apoptosis in pterygium epithelial cells. Pterygium epithelial cells were transfected with the miR-122 inhibitor (100 nM) with or without Bcl-w <t>siRNA/</t> control siRNA (50 nM) as indicated followed by stimulation with TNFa (20 ng/mL) plus/CHX (25 lg/mL) for 4 hours. (A) Tumor necrosis factor a/CHX-induced apoptosis of pterygium epithelial cells was determined by TUNEL/DAPI staining. (B) The percentage of apoptotic cells was calculated and plotted. Values are mean 6 SD from three separate experiments. *P < 0.05 compared with the control; #P < 0.05 compared with the cells stimulated by only miR-122 inhibitor. (C) Caspase 3/7 activity in pterygium epithelial cells was determined with Caspase-Glo 3/7 assay kit (Promega). Values are mean 6 SD from three separate experiments. *P < 0.05, comparison between the two indicated groups; #P < 0.05, comparison between the two indicated groups.
Af8241 Bcl Xl Wb N A Rabbit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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bclw dna  (OriGene)
90
OriGene bclw dna
FIGURE 6. The effect of miR-122 on TNFa/CHX induced apoptosis in pterygium epithelial cells. Pterygium epithelial cells were transfected with the miR-122 inhibitor (100 nM) with or without Bcl-w <t>siRNA/</t> control siRNA (50 nM) as indicated followed by stimulation with TNFa (20 ng/mL) plus/CHX (25 lg/mL) for 4 hours. (A) Tumor necrosis factor a/CHX-induced apoptosis of pterygium epithelial cells was determined by TUNEL/DAPI staining. (B) The percentage of apoptotic cells was calculated and plotted. Values are mean 6 SD from three separate experiments. *P < 0.05 compared with the control; #P < 0.05 compared with the cells stimulated by only miR-122 inhibitor. (C) Caspase 3/7 activity in pterygium epithelial cells was determined with Caspase-Glo 3/7 assay kit (Promega). Values are mean 6 SD from three separate experiments. *P < 0.05, comparison between the two indicated groups; #P < 0.05, comparison between the two indicated groups.
Bclw Dna, supplied by OriGene, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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rabbit polyclonal antibody  (R&D Systems)
90
R&D Systems rabbit polyclonal antibody
FIG. 2. Expression of Bclw in Sertoli cells during the first wave of spermatogenesis. (A) Western analysis of total testis extracts from mice at age 10 days (10), 17 days (17), 25 days (25), adult (A), and from a testis from a Bclw2/2 adult mouse (2/2). (Left) Blot reacted with a <t>polyclonal</t> antibody that recognizes the 21-kDa BCLW protein (arrow), which is absent in the homozygous mutant. (Right) The same blot stained with Ponceau S to show relative amount of protein loaded in each lane. In addition to BCLW, the antisera also reacts with nonspecific proteins of approximately 18, 42, and 65 kDa. The absence of the 42- and 65-kDa species in the sample from the Bclw 2/2 is most likely due to these proteins being expressed in germ cells that are absent in this sample. (B) In situ analysis of Bclw mRNA expression in testes from animals at postnatal days 10, 17, and 25. (Top row) Sections from testis from a wild-type (1/1) mouse reacted with the Bclw anti-sense probe. Cells
Rabbit Polyclonal Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


FIGURE 6. The effect of miR-122 on TNFa/CHX induced apoptosis in pterygium epithelial cells. Pterygium epithelial cells were transfected with the miR-122 inhibitor (100 nM) with or without Bcl-w siRNA/ control siRNA (50 nM) as indicated followed by stimulation with TNFa (20 ng/mL) plus/CHX (25 lg/mL) for 4 hours. (A) Tumor necrosis factor a/CHX-induced apoptosis of pterygium epithelial cells was determined by TUNEL/DAPI staining. (B) The percentage of apoptotic cells was calculated and plotted. Values are mean 6 SD from three separate experiments. *P < 0.05 compared with the control; #P < 0.05 compared with the cells stimulated by only miR-122 inhibitor. (C) Caspase 3/7 activity in pterygium epithelial cells was determined with Caspase-Glo 3/7 assay kit (Promega). Values are mean 6 SD from three separate experiments. *P < 0.05, comparison between the two indicated groups; #P < 0.05, comparison between the two indicated groups.

Journal: Investigative ophthalmology & visual science

Article Title: Regulation of Apoptosis by miR-122 in Pterygium via Targeting Bcl-w.

doi: 10.1167/iovs.16-19402

Figure Lengend Snippet: FIGURE 6. The effect of miR-122 on TNFa/CHX induced apoptosis in pterygium epithelial cells. Pterygium epithelial cells were transfected with the miR-122 inhibitor (100 nM) with or without Bcl-w siRNA/ control siRNA (50 nM) as indicated followed by stimulation with TNFa (20 ng/mL) plus/CHX (25 lg/mL) for 4 hours. (A) Tumor necrosis factor a/CHX-induced apoptosis of pterygium epithelial cells was determined by TUNEL/DAPI staining. (B) The percentage of apoptotic cells was calculated and plotted. Values are mean 6 SD from three separate experiments. *P < 0.05 compared with the control; #P < 0.05 compared with the cells stimulated by only miR-122 inhibitor. (C) Caspase 3/7 activity in pterygium epithelial cells was determined with Caspase-Glo 3/7 assay kit (Promega). Values are mean 6 SD from three separate experiments. *P < 0.05, comparison between the two indicated groups; #P < 0.05, comparison between the two indicated groups.

Article Snippet: Bclw antibody, Bcl-w specific siRNA, control siRNA, horseradish peroxidase-conjugated secondary antibody, and FITC-labeled secondary antibody were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA).

Techniques: Transfection, Control, TUNEL Assay, Staining, Activity Assay, Caspase-Glo Assay, Comparison

FIG. 2. Expression of Bclw in Sertoli cells during the first wave of spermatogenesis. (A) Western analysis of total testis extracts from mice at age 10 days (10), 17 days (17), 25 days (25), adult (A), and from a testis from a Bclw2/2 adult mouse (2/2). (Left) Blot reacted with a polyclonal antibody that recognizes the 21-kDa BCLW protein (arrow), which is absent in the homozygous mutant. (Right) The same blot stained with Ponceau S to show relative amount of protein loaded in each lane. In addition to BCLW, the antisera also reacts with nonspecific proteins of approximately 18, 42, and 65 kDa. The absence of the 42- and 65-kDa species in the sample from the Bclw 2/2 is most likely due to these proteins being expressed in germ cells that are absent in this sample. (B) In situ analysis of Bclw mRNA expression in testes from animals at postnatal days 10, 17, and 25. (Top row) Sections from testis from a wild-type (1/1) mouse reacted with the Bclw anti-sense probe. Cells

Journal: Developmental biology

Article Title: BCLW mediates survival of postmitotic Sertoli cells by regulating BAX activity.

doi: 10.1006/dbio.2001.0445

Figure Lengend Snippet: FIG. 2. Expression of Bclw in Sertoli cells during the first wave of spermatogenesis. (A) Western analysis of total testis extracts from mice at age 10 days (10), 17 days (17), 25 days (25), adult (A), and from a testis from a Bclw2/2 adult mouse (2/2). (Left) Blot reacted with a polyclonal antibody that recognizes the 21-kDa BCLW protein (arrow), which is absent in the homozygous mutant. (Right) The same blot stained with Ponceau S to show relative amount of protein loaded in each lane. In addition to BCLW, the antisera also reacts with nonspecific proteins of approximately 18, 42, and 65 kDa. The absence of the 42- and 65-kDa species in the sample from the Bclw 2/2 is most likely due to these proteins being expressed in germ cells that are absent in this sample. (B) In situ analysis of Bclw mRNA expression in testes from animals at postnatal days 10, 17, and 25. (Top row) Sections from testis from a wild-type (1/1) mouse reacted with the Bclw anti-sense probe. Cells

Article Snippet: For BCLW Western analysis, a rabbit polyclonal antibody from R&D Systems, Inc. (Minneapolis, MN; catalog # AF824) was used.

Techniques: Expressing, Western Blot, Mutagenesis, Staining, In Situ