454 Search Results


94
ATCC dr marco fiocchetti
Dr Marco Fiocchetti, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ATCC c tetani atcc 454
C Tetani Atcc 454, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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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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Thermo Fisher advanced mirna hsa mir 454 5p 478919 mir
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.
Advanced Mirna Hsa Mir 454 5p 478919 Mir, supplied by Thermo Fisher, 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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Miltenyi Biotec cd4 t cell isolation kit
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.
Cd4 T Cell Isolation Kit, supplied by Miltenyi Biotec, 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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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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ProSci Incorporated sucrose
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.
Sucrose, supplied by ProSci Incorporated, 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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Miltenyi Biotec noggin
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.
Noggin, 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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Miltenyi Biotec rea control rea293 recombinant human igg1
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.
Rea Control Rea293 Recombinant Human Igg1, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Miltenyi Biotec miltenyi biotec cd8a
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.
Miltenyi Biotec Cd8a, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Chem Impex International aza
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.
Aza, supplied by Chem Impex International, 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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88
DSMZ k racemifer dsm44963
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.
K Racemifer Dsm44963, supplied by DSMZ, used in various techniques. Bioz Stars score: 88/100, 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