est database generated with 454 Search Results


454 bu  (ATCC)
95
ATCC 454 bu
454 Bu, supplied by ATCC, 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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btn-flt3  (Carna Inc)
93
Carna Inc btn-flt3
Btn Flt3, supplied by Carna Inc, 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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cpla2 antibody  (Santa Cruz Biotechnology)
96
Santa Cruz Biotechnology cpla2 antibody
FIG. 3. Integrin-dependent phosphorylation of <t>cPLA2</t> and re- lease of arachidonic acid metabolites are Ras-dependent. A, lysates prepared from parental (3T3) or N17Ras-expressing (DN2) NIH3T3 cells were prepared as described in the legend to Fig. 2. 10 mg of lysate were electrophoresed and cPLA2 activation was analyzed by immunoblotting with a cPLA2 antibody to detect the mobility shift. The slower migrating band indicates the activated (phosphorylated) form of cPLA2 (cPLA2P). B, [3H]arachidonic acid-labeled cells were washed and plated onto fibronectin- (FN) or polylysine- (pL) coated plates, and the release of [3H]arachidonic acid was assayed as described under “Exper- imental Procedures.” The data shown represent the average of tripli- cate samples 6 S.D., from a typical experiment conducted three times.
Cpla2 Antibody, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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gene exp il1b mm00434228 m1  (Thermo Fisher)
99
Thermo Fisher gene exp il1b mm00434228 m1
FIG. 3. Integrin-dependent phosphorylation of <t>cPLA2</t> and re- lease of arachidonic acid metabolites are Ras-dependent. A, lysates prepared from parental (3T3) or N17Ras-expressing (DN2) NIH3T3 cells were prepared as described in the legend to Fig. 2. 10 mg of lysate were electrophoresed and cPLA2 activation was analyzed by immunoblotting with a cPLA2 antibody to detect the mobility shift. The slower migrating band indicates the activated (phosphorylated) form of cPLA2 (cPLA2P). B, [3H]arachidonic acid-labeled cells were washed and plated onto fibronectin- (FN) or polylysine- (pL) coated plates, and the release of [3H]arachidonic acid was assayed as described under “Exper- imental Procedures.” The data shown represent the average of tripli- cate samples 6 S.D., from a typical experiment conducted three times.
Gene Exp Il1b Mm00434228 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mir 454 3p expression  (Genecopoeia)
96
Genecopoeia mir 454 3p expression
FIG. 3. Integrin-dependent phosphorylation of <t>cPLA2</t> and re- lease of arachidonic acid metabolites are Ras-dependent. A, lysates prepared from parental (3T3) or N17Ras-expressing (DN2) NIH3T3 cells were prepared as described in the legend to Fig. 2. 10 mg of lysate were electrophoresed and cPLA2 activation was analyzed by immunoblotting with a cPLA2 antibody to detect the mobility shift. The slower migrating band indicates the activated (phosphorylated) form of cPLA2 (cPLA2P). B, [3H]arachidonic acid-labeled cells were washed and plated onto fibronectin- (FN) or polylysine- (pL) coated plates, and the release of [3H]arachidonic acid was assayed as described under “Exper- imental Procedures.” The data shown represent the average of tripli- cate samples 6 S.D., from a typical experiment conducted three times.
Mir 454 3p Expression, supplied by Genecopoeia, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fems microbiol ecol 79 (2012) 454–464  (Federation of European Neuroscience Societies)
90
Federation of European Neuroscience Societies fems microbiol ecol 79 (2012) 454–464
FIG. 3. Integrin-dependent phosphorylation of <t>cPLA2</t> and re- lease of arachidonic acid metabolites are Ras-dependent. A, lysates prepared from parental (3T3) or N17Ras-expressing (DN2) NIH3T3 cells were prepared as described in the legend to Fig. 2. 10 mg of lysate were electrophoresed and cPLA2 activation was analyzed by immunoblotting with a cPLA2 antibody to detect the mobility shift. The slower migrating band indicates the activated (phosphorylated) form of cPLA2 (cPLA2P). B, [3H]arachidonic acid-labeled cells were washed and plated onto fibronectin- (FN) or polylysine- (pL) coated plates, and the release of [3H]arachidonic acid was assayed as described under “Exper- imental Procedures.” The data shown represent the average of tripli- cate samples 6 S.D., from a typical experiment conducted three times.
Fems Microbiol Ecol 79 (2012) 454–464, supplied by Federation of European Neuroscience Societies, 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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454 sequencing reads  (Vertis Biotechnologie)
90
Vertis Biotechnologie 454 sequencing reads
FIG. 3. Integrin-dependent phosphorylation of <t>cPLA2</t> and re- lease of arachidonic acid metabolites are Ras-dependent. A, lysates prepared from parental (3T3) or N17Ras-expressing (DN2) NIH3T3 cells were prepared as described in the legend to Fig. 2. 10 mg of lysate were electrophoresed and cPLA2 activation was analyzed by immunoblotting with a cPLA2 antibody to detect the mobility shift. The slower migrating band indicates the activated (phosphorylated) form of cPLA2 (cPLA2P). B, [3H]arachidonic acid-labeled cells were washed and plated onto fibronectin- (FN) or polylysine- (pL) coated plates, and the release of [3H]arachidonic acid was assayed as described under “Exper- imental Procedures.” The data shown represent the average of tripli- cate samples 6 S.D., from a typical experiment conducted three times.
454 Sequencing Reads, supplied by Vertis Biotechnologie, 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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liquichektm qualitative urine toxicology control  (Bio-Rad)
85
Bio-Rad liquichektm qualitative urine toxicology control
FIG. 3. Integrin-dependent phosphorylation of <t>cPLA2</t> and re- lease of arachidonic acid metabolites are Ras-dependent. A, lysates prepared from parental (3T3) or N17Ras-expressing (DN2) NIH3T3 cells were prepared as described in the legend to Fig. 2. 10 mg of lysate were electrophoresed and cPLA2 activation was analyzed by immunoblotting with a cPLA2 antibody to detect the mobility shift. The slower migrating band indicates the activated (phosphorylated) form of cPLA2 (cPLA2P). B, [3H]arachidonic acid-labeled cells were washed and plated onto fibronectin- (FN) or polylysine- (pL) coated plates, and the release of [3H]arachidonic acid was assayed as described under “Exper- imental Procedures.” The data shown represent the average of tripli- cate samples 6 S.D., from a typical experiment conducted three times.
Liquichektm Qualitative Urine Toxicology Control, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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454 flx cdna libraries  (CLC Bio)
90
CLC Bio 454 flx cdna libraries
FIG. 3. Integrin-dependent phosphorylation of <t>cPLA2</t> and re- lease of arachidonic acid metabolites are Ras-dependent. A, lysates prepared from parental (3T3) or N17Ras-expressing (DN2) NIH3T3 cells were prepared as described in the legend to Fig. 2. 10 mg of lysate were electrophoresed and cPLA2 activation was analyzed by immunoblotting with a cPLA2 antibody to detect the mobility shift. The slower migrating band indicates the activated (phosphorylated) form of cPLA2 (cPLA2P). B, [3H]arachidonic acid-labeled cells were washed and plated onto fibronectin- (FN) or polylysine- (pL) coated plates, and the release of [3H]arachidonic acid was assayed as described under “Exper- imental Procedures.” The data shown represent the average of tripli- cate samples 6 S.D., from a typical experiment conducted three times.
454 Flx Cdna Libraries, supplied by CLC Bio, 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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454 flx  (LGC Genomics GmbH)
90
LGC Genomics GmbH 454 flx
FIG. 3. Integrin-dependent phosphorylation of <t>cPLA2</t> and re- lease of arachidonic acid metabolites are Ras-dependent. A, lysates prepared from parental (3T3) or N17Ras-expressing (DN2) NIH3T3 cells were prepared as described in the legend to Fig. 2. 10 mg of lysate were electrophoresed and cPLA2 activation was analyzed by immunoblotting with a cPLA2 antibody to detect the mobility shift. The slower migrating band indicates the activated (phosphorylated) form of cPLA2 (cPLA2P). B, [3H]arachidonic acid-labeled cells were washed and plated onto fibronectin- (FN) or polylysine- (pL) coated plates, and the release of [3H]arachidonic acid was assayed as described under “Exper- imental Procedures.” The data shown represent the average of tripli- cate samples 6 S.D., from a typical experiment conducted three times.
454 Flx, supplied by LGC Genomics GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/454 flx/product/LGC Genomics GmbH
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recombinant human noggin protein  (Miltenyi Biotec)
95
Miltenyi Biotec recombinant human noggin protein
FIG. 3. Integrin-dependent phosphorylation of <t>cPLA2</t> and re- lease of arachidonic acid metabolites are Ras-dependent. A, lysates prepared from parental (3T3) or N17Ras-expressing (DN2) NIH3T3 cells were prepared as described in the legend to Fig. 2. 10 mg of lysate were electrophoresed and cPLA2 activation was analyzed by immunoblotting with a cPLA2 antibody to detect the mobility shift. The slower migrating band indicates the activated (phosphorylated) form of cPLA2 (cPLA2P). B, [3H]arachidonic acid-labeled cells were washed and plated onto fibronectin- (FN) or polylysine- (pL) coated plates, and the release of [3H]arachidonic acid was assayed as described under “Exper- imental Procedures.” The data shown represent the average of tripli- cate samples 6 S.D., from a typical experiment conducted three times.
Recombinant Human Noggin Protein, supplied by Miltenyi Biotec, 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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mavs  (Santa Cruz Biotechnology)
96
Santa Cruz Biotechnology mavs
FIG. 3. Integrin-dependent phosphorylation of <t>cPLA2</t> and re- lease of arachidonic acid metabolites are Ras-dependent. A, lysates prepared from parental (3T3) or N17Ras-expressing (DN2) NIH3T3 cells were prepared as described in the legend to Fig. 2. 10 mg of lysate were electrophoresed and cPLA2 activation was analyzed by immunoblotting with a cPLA2 antibody to detect the mobility shift. The slower migrating band indicates the activated (phosphorylated) form of cPLA2 (cPLA2P). B, [3H]arachidonic acid-labeled cells were washed and plated onto fibronectin- (FN) or polylysine- (pL) coated plates, and the release of [3H]arachidonic acid was assayed as described under “Exper- imental Procedures.” The data shown represent the average of tripli- cate samples 6 S.D., from a typical experiment conducted three times.
Mavs, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


FIG. 3. Integrin-dependent phosphorylation of cPLA2 and re- lease of arachidonic acid metabolites are Ras-dependent. A, lysates prepared from parental (3T3) or N17Ras-expressing (DN2) NIH3T3 cells were prepared as described in the legend to Fig. 2. 10 mg of lysate were electrophoresed and cPLA2 activation was analyzed by immunoblotting with a cPLA2 antibody to detect the mobility shift. The slower migrating band indicates the activated (phosphorylated) form of cPLA2 (cPLA2P). B, [3H]arachidonic acid-labeled cells were washed and plated onto fibronectin- (FN) or polylysine- (pL) coated plates, and the release of [3H]arachidonic acid was assayed as described under “Exper- imental Procedures.” The data shown represent the average of tripli- cate samples 6 S.D., from a typical experiment conducted three times.

Journal: The Journal of biological chemistry

Article Title: Ras activation is necessary for integrin-mediated activation of extracellular signal-regulated kinase 2 and cytosolic phospholipase A2 but not for cytoskeletal organization.

doi: 10.1074/jbc.271.25.14814

Figure Lengend Snippet: FIG. 3. Integrin-dependent phosphorylation of cPLA2 and re- lease of arachidonic acid metabolites are Ras-dependent. A, lysates prepared from parental (3T3) or N17Ras-expressing (DN2) NIH3T3 cells were prepared as described in the legend to Fig. 2. 10 mg of lysate were electrophoresed and cPLA2 activation was analyzed by immunoblotting with a cPLA2 antibody to detect the mobility shift. The slower migrating band indicates the activated (phosphorylated) form of cPLA2 (cPLA2P). B, [3H]arachidonic acid-labeled cells were washed and plated onto fibronectin- (FN) or polylysine- (pL) coated plates, and the release of [3H]arachidonic acid was assayed as described under “Exper- imental Procedures.” The data shown represent the average of tripli- cate samples 6 S.D., from a typical experiment conducted three times.

Article Snippet: The cPLA2 antibody was purchased from Santa Cruz Biotech.

Techniques: Phospho-proteomics, Expressing, Activation Assay, Western Blot, Mobility Shift, Labeling