rabbit anti- p- perk primary antibody (cat Search Results


cat-1 antibody  (Rockland Immunochemicals)
90
Rockland Immunochemicals cat-1 antibody
Cat 1 Antibody, supplied by Rockland Immunochemicals, 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/cat-1 antibody/product/Rockland Immunochemicals
Average 90 stars, based on 1 article reviews
cat-1 antibody - by Bioz Stars, 2026-03
90/100 stars
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primary antibody rabbit anti-c-fos igg [cat.no. sc-52]  (FD NeuroTechnologies)
90
FD NeuroTechnologies primary antibody rabbit anti-c-fos igg [cat.no. sc-52]
Primary Antibody Rabbit Anti C Fos Igg [Cat.No. Sc 52], supplied by FD NeuroTechnologies, 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/primary antibody rabbit anti-c-fos igg [cat.no. sc-52]/product/FD NeuroTechnologies
Average 90 stars, based on 1 article reviews
primary antibody rabbit anti-c-fos igg [cat.no. sc-52] - by Bioz Stars, 2026-03
90/100 stars
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rabbit anti-human p38mapk/p-p38mapk  (Bioworld Antibodies)
90
Bioworld Antibodies rabbit anti-human p38mapk/p-p38mapk
(A) The migration in wound-healing assay of A549 cells after treatment with DMSO or E2 (10 nM), PPT (10 nM), DPN (10 nM), E2+Ful (1 μM) and Ful (1 μM) for 24 h (magnification 40×); (B) The effect on wound closure (percentage) in A549 cells ( *p < 0.05 vs. control group, #p < 0.05 vs. E2 group ); (C) Representative images of Transwell assays to assess A549 cell invasion and migration; (D) The effect of transwell migration assays in A549 cells after treating with DMSO or E2 (10 nM), PPT (10 nM), DPN (10 nM), E2+Ful (1μM) and Ful(1μM) for 24 h; The effect of transwell migration assays in H1793 cells after treatment with the same drugs for 72 h; (E) Representative images of Transwell assays for assessment of H1793 cell invasion and migration; (F) The effect of transwell migration assays in H1793 cells after treatment with DMSO or E2 (10 nM), PPT (10 nM), DPN (10 nM), E2+Ful (1 μM) and Ful (1 μM) for 24 h. The effect of transwell migration assays in H1793 cells after treatment with the same drugs for 72 h; (G-H) Western blot analysis of <t>ERβ,</t> <t>MMP-2,</t> MMP-9, p-p38MAPK, p38MAPK, pAKT and <t>tAKT</t> protein levels at 48 h in A549 cells, respectively. GAPDH was used as a control. All data are shown as the mean ± SD. Results represent three independent experiments. Student's t-test was carried out ( *p < 0.05 vs. control group, #p < 0.05 vs. E2 group ).
Rabbit Anti Human P38mapk/P P38mapk, supplied by Bioworld Antibodies, 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/rabbit anti-human p38mapk/p-p38mapk/product/Bioworld Antibodies
Average 90 stars, based on 1 article reviews
rabbit anti-human p38mapk/p-p38mapk - by Bioz Stars, 2026-03
90/100 stars
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rabbit anti-tyrosine hydroxylase primary antibody (1/2000 dilution, cat # 2025-thrab, rrid:ab2492276  (PhosphoSolutions)
90
PhosphoSolutions rabbit anti-tyrosine hydroxylase primary antibody (1/2000 dilution, cat # 2025-thrab, rrid:ab2492276
(A) The migration in wound-healing assay of A549 cells after treatment with DMSO or E2 (10 nM), PPT (10 nM), DPN (10 nM), E2+Ful (1 μM) and Ful (1 μM) for 24 h (magnification 40×); (B) The effect on wound closure (percentage) in A549 cells ( *p < 0.05 vs. control group, #p < 0.05 vs. E2 group ); (C) Representative images of Transwell assays to assess A549 cell invasion and migration; (D) The effect of transwell migration assays in A549 cells after treating with DMSO or E2 (10 nM), PPT (10 nM), DPN (10 nM), E2+Ful (1μM) and Ful(1μM) for 24 h; The effect of transwell migration assays in H1793 cells after treatment with the same drugs for 72 h; (E) Representative images of Transwell assays for assessment of H1793 cell invasion and migration; (F) The effect of transwell migration assays in H1793 cells after treatment with DMSO or E2 (10 nM), PPT (10 nM), DPN (10 nM), E2+Ful (1 μM) and Ful (1 μM) for 24 h. The effect of transwell migration assays in H1793 cells after treatment with the same drugs for 72 h; (G-H) Western blot analysis of <t>ERβ,</t> <t>MMP-2,</t> MMP-9, p-p38MAPK, p38MAPK, pAKT and <t>tAKT</t> protein levels at 48 h in A549 cells, respectively. GAPDH was used as a control. All data are shown as the mean ± SD. Results represent three independent experiments. Student's t-test was carried out ( *p < 0.05 vs. control group, #p < 0.05 vs. E2 group ).
Rabbit Anti Tyrosine Hydroxylase Primary Antibody (1/2000 Dilution, Cat # 2025 Thrab, Rrid:Ab2492276, supplied by PhosphoSolutions, 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/rabbit anti-tyrosine hydroxylase primary antibody (1/2000 dilution, cat # 2025-thrab, rrid:ab2492276/product/PhosphoSolutions
Average 90 stars, based on 1 article reviews
rabbit anti-tyrosine hydroxylase primary antibody (1/2000 dilution, cat # 2025-thrab, rrid:ab2492276 - by Bioz Stars, 2026-03
90/100 stars
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primary rabbit polyclonal anti-zo-1 antibody cat# e-ab-18170  (Elabscience Biotechnology)
90
Elabscience Biotechnology primary rabbit polyclonal anti-zo-1 antibody cat# e-ab-18170
(A) The migration in wound-healing assay of A549 cells after treatment with DMSO or E2 (10 nM), PPT (10 nM), DPN (10 nM), E2+Ful (1 μM) and Ful (1 μM) for 24 h (magnification 40×); (B) The effect on wound closure (percentage) in A549 cells ( *p < 0.05 vs. control group, #p < 0.05 vs. E2 group ); (C) Representative images of Transwell assays to assess A549 cell invasion and migration; (D) The effect of transwell migration assays in A549 cells after treating with DMSO or E2 (10 nM), PPT (10 nM), DPN (10 nM), E2+Ful (1μM) and Ful(1μM) for 24 h; The effect of transwell migration assays in H1793 cells after treatment with the same drugs for 72 h; (E) Representative images of Transwell assays for assessment of H1793 cell invasion and migration; (F) The effect of transwell migration assays in H1793 cells after treatment with DMSO or E2 (10 nM), PPT (10 nM), DPN (10 nM), E2+Ful (1 μM) and Ful (1 μM) for 24 h. The effect of transwell migration assays in H1793 cells after treatment with the same drugs for 72 h; (G-H) Western blot analysis of <t>ERβ,</t> <t>MMP-2,</t> MMP-9, p-p38MAPK, p38MAPK, pAKT and <t>tAKT</t> protein levels at 48 h in A549 cells, respectively. GAPDH was used as a control. All data are shown as the mean ± SD. Results represent three independent experiments. Student's t-test was carried out ( *p < 0.05 vs. control group, #p < 0.05 vs. E2 group ).
Primary Rabbit Polyclonal Anti Zo 1 Antibody Cat# E Ab 18170, supplied by Elabscience Biotechnology, 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/primary rabbit polyclonal anti-zo-1 antibody cat# e-ab-18170/product/Elabscience Biotechnology
Average 90 stars, based on 1 article reviews
primary rabbit polyclonal anti-zo-1 antibody cat# e-ab-18170 - by Bioz Stars, 2026-03
90/100 stars
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polyclonal rabbit anti-human anti-p akt (ser473) antibody (cat no. bs4006)  (Bioworld Antibodies)
90
Bioworld Antibodies polyclonal rabbit anti-human anti-p akt (ser473) antibody (cat no. bs4006)
(A) The migration in wound-healing assay of A549 cells after treatment with DMSO or E2 (10 nM), PPT (10 nM), DPN (10 nM), E2+Ful (1 μM) and Ful (1 μM) for 24 h (magnification 40×); (B) The effect on wound closure (percentage) in A549 cells ( *p < 0.05 vs. control group, #p < 0.05 vs. E2 group ); (C) Representative images of Transwell assays to assess A549 cell invasion and migration; (D) The effect of transwell migration assays in A549 cells after treating with DMSO or E2 (10 nM), PPT (10 nM), DPN (10 nM), E2+Ful (1μM) and Ful(1μM) for 24 h; The effect of transwell migration assays in H1793 cells after treatment with the same drugs for 72 h; (E) Representative images of Transwell assays for assessment of H1793 cell invasion and migration; (F) The effect of transwell migration assays in H1793 cells after treatment with DMSO or E2 (10 nM), PPT (10 nM), DPN (10 nM), E2+Ful (1 μM) and Ful (1 μM) for 24 h. The effect of transwell migration assays in H1793 cells after treatment with the same drugs for 72 h; (G-H) Western blot analysis of <t>ERβ,</t> <t>MMP-2,</t> MMP-9, p-p38MAPK, p38MAPK, pAKT and <t>tAKT</t> protein levels at 48 h in A549 cells, respectively. GAPDH was used as a control. All data are shown as the mean ± SD. Results represent three independent experiments. Student's t-test was carried out ( *p < 0.05 vs. control group, #p < 0.05 vs. E2 group ).
Polyclonal Rabbit Anti Human Anti P Akt (Ser473) Antibody (Cat No. Bs4006), supplied by Bioworld Antibodies, 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/polyclonal rabbit anti-human anti-p akt (ser473) antibody (cat no. bs4006)/product/Bioworld Antibodies
Average 90 stars, based on 1 article reviews
polyclonal rabbit anti-human anti-p akt (ser473) antibody (cat no. bs4006) - by Bioz Stars, 2026-03
90/100 stars
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Image Search Results


(A) The migration in wound-healing assay of A549 cells after treatment with DMSO or E2 (10 nM), PPT (10 nM), DPN (10 nM), E2+Ful (1 μM) and Ful (1 μM) for 24 h (magnification 40×); (B) The effect on wound closure (percentage) in A549 cells ( *p < 0.05 vs. control group, #p < 0.05 vs. E2 group ); (C) Representative images of Transwell assays to assess A549 cell invasion and migration; (D) The effect of transwell migration assays in A549 cells after treating with DMSO or E2 (10 nM), PPT (10 nM), DPN (10 nM), E2+Ful (1μM) and Ful(1μM) for 24 h; The effect of transwell migration assays in H1793 cells after treatment with the same drugs for 72 h; (E) Representative images of Transwell assays for assessment of H1793 cell invasion and migration; (F) The effect of transwell migration assays in H1793 cells after treatment with DMSO or E2 (10 nM), PPT (10 nM), DPN (10 nM), E2+Ful (1 μM) and Ful (1 μM) for 24 h. The effect of transwell migration assays in H1793 cells after treatment with the same drugs for 72 h; (G-H) Western blot analysis of ERβ, MMP-2, MMP-9, p-p38MAPK, p38MAPK, pAKT and tAKT protein levels at 48 h in A549 cells, respectively. GAPDH was used as a control. All data are shown as the mean ± SD. Results represent three independent experiments. Student's t-test was carried out ( *p < 0.05 vs. control group, #p < 0.05 vs. E2 group ).

Journal: Oncotarget

Article Title: Estrogen promotes tumor metastasis via estrogen receptor beta-mediated regulation of matrix-metalloproteinase-2 in non-small cell lung cancer

doi: 10.18632/oncotarget.16992

Figure Lengend Snippet: (A) The migration in wound-healing assay of A549 cells after treatment with DMSO or E2 (10 nM), PPT (10 nM), DPN (10 nM), E2+Ful (1 μM) and Ful (1 μM) for 24 h (magnification 40×); (B) The effect on wound closure (percentage) in A549 cells ( *p < 0.05 vs. control group, #p < 0.05 vs. E2 group ); (C) Representative images of Transwell assays to assess A549 cell invasion and migration; (D) The effect of transwell migration assays in A549 cells after treating with DMSO or E2 (10 nM), PPT (10 nM), DPN (10 nM), E2+Ful (1μM) and Ful(1μM) for 24 h; The effect of transwell migration assays in H1793 cells after treatment with the same drugs for 72 h; (E) Representative images of Transwell assays for assessment of H1793 cell invasion and migration; (F) The effect of transwell migration assays in H1793 cells after treatment with DMSO or E2 (10 nM), PPT (10 nM), DPN (10 nM), E2+Ful (1 μM) and Ful (1 μM) for 24 h. The effect of transwell migration assays in H1793 cells after treatment with the same drugs for 72 h; (G-H) Western blot analysis of ERβ, MMP-2, MMP-9, p-p38MAPK, p38MAPK, pAKT and tAKT protein levels at 48 h in A549 cells, respectively. GAPDH was used as a control. All data are shown as the mean ± SD. Results represent three independent experiments. Student's t-test was carried out ( *p < 0.05 vs. control group, #p < 0.05 vs. E2 group ).

Article Snippet: The antibodies used during Western blots included rabbit anti-human ERα from Proteintech, rabbit anti-human ERβ (1:500) from Proteintech, mouse anti-human MMP-1(1:400) from Santa Cruz, mouse anti-human MMP-2(1:400) from Santa Cruz, rabbit anti-human MMP-9 (1:500) from Proteintech, rabbit anti-human p38MAPK(1:500)/p-p38MAPK(1:500) and rabbit anti-human tAkt (1:500)/pAkt(1:500) from Bioworld Technology.

Techniques: Migration, Wound Healing Assay, Western Blot

(A) Western blot analysis of protein expression of ERβ, MMP-2, p-p38MAPK, p38MAPK, pAKT and tAKT in NSCLC cell line A549 when treating with DMSO or E2 (10 nM), E2+LY294002 (10 nM), LY294002 (10 nM), E2+SB203580 (10 nM) and SB203590 (10 nM) for 48 h. (B) the detection of optical density. GAPDH was used as a control. All data are shown as the mean ± SD. Results represent three independent experiments. Student's t-test was carried out ( *p < 0.05 vs. control group, #p < 0.05 vs. E2 group ).

Journal: Oncotarget

Article Title: Estrogen promotes tumor metastasis via estrogen receptor beta-mediated regulation of matrix-metalloproteinase-2 in non-small cell lung cancer

doi: 10.18632/oncotarget.16992

Figure Lengend Snippet: (A) Western blot analysis of protein expression of ERβ, MMP-2, p-p38MAPK, p38MAPK, pAKT and tAKT in NSCLC cell line A549 when treating with DMSO or E2 (10 nM), E2+LY294002 (10 nM), LY294002 (10 nM), E2+SB203580 (10 nM) and SB203590 (10 nM) for 48 h. (B) the detection of optical density. GAPDH was used as a control. All data are shown as the mean ± SD. Results represent three independent experiments. Student's t-test was carried out ( *p < 0.05 vs. control group, #p < 0.05 vs. E2 group ).

Article Snippet: The antibodies used during Western blots included rabbit anti-human ERα from Proteintech, rabbit anti-human ERβ (1:500) from Proteintech, mouse anti-human MMP-1(1:400) from Santa Cruz, mouse anti-human MMP-2(1:400) from Santa Cruz, rabbit anti-human MMP-9 (1:500) from Proteintech, rabbit anti-human p38MAPK(1:500)/p-p38MAPK(1:500) and rabbit anti-human tAkt (1:500)/pAkt(1:500) from Bioworld Technology.

Techniques: Western Blot, Expressing

(A) After bilateral ovariectomy A549 cells (5 × 10 6 /100 μL) suspended in PBS were injected into 4-week-old female BALB/c nude mice via the tail vein, mice were randomly divided into five groups (N = 5/group): E2(0.09 mg/kg), PPT(1.05 mg/kg), DPN(1.89 mg/kg), E2+ Ful(1.46 mg/kg) and blank control. The lungs were removed after 4 weeks subcutaneously under drug treatment. Gross appearance of metastatic lung tumor nodes in different groups is indicated by bright yellow arrows. (B) Representative pathological image of metastatic A549 tumor at magnification 100ificatione pathological image of groups (N = 5/group): The number of metastatic nodules in the lungs (lung nodules number in every mouse of each group), metastatic index in different groups mentioned in ‘‘Materials and methods’’ section for the experimental. (C-E) The mean lung wet weight of each group, The number of metastatic nodules in the lungs (lung nodules number in every mouse of each group), metastatic index in different groups mentioned in ‘‘Materials and methods’’ section for the experimental. (F) Protein expression of ERβ, MMP-2, MMP-9, p-p38MAPK, p38MAPK, pAKT and tAKT in murine lung metastatic nodes was analyzed using Western blot, and (G) the detection of optical density. All data are expressed as the mean ± SD. Student's t-test was carried out ( *p < 0.05 vs. control group, #p < 0.05 vs. E2 group ).

Journal: Oncotarget

Article Title: Estrogen promotes tumor metastasis via estrogen receptor beta-mediated regulation of matrix-metalloproteinase-2 in non-small cell lung cancer

doi: 10.18632/oncotarget.16992

Figure Lengend Snippet: (A) After bilateral ovariectomy A549 cells (5 × 10 6 /100 μL) suspended in PBS were injected into 4-week-old female BALB/c nude mice via the tail vein, mice were randomly divided into five groups (N = 5/group): E2(0.09 mg/kg), PPT(1.05 mg/kg), DPN(1.89 mg/kg), E2+ Ful(1.46 mg/kg) and blank control. The lungs were removed after 4 weeks subcutaneously under drug treatment. Gross appearance of metastatic lung tumor nodes in different groups is indicated by bright yellow arrows. (B) Representative pathological image of metastatic A549 tumor at magnification 100ificatione pathological image of groups (N = 5/group): The number of metastatic nodules in the lungs (lung nodules number in every mouse of each group), metastatic index in different groups mentioned in ‘‘Materials and methods’’ section for the experimental. (C-E) The mean lung wet weight of each group, The number of metastatic nodules in the lungs (lung nodules number in every mouse of each group), metastatic index in different groups mentioned in ‘‘Materials and methods’’ section for the experimental. (F) Protein expression of ERβ, MMP-2, MMP-9, p-p38MAPK, p38MAPK, pAKT and tAKT in murine lung metastatic nodes was analyzed using Western blot, and (G) the detection of optical density. All data are expressed as the mean ± SD. Student's t-test was carried out ( *p < 0.05 vs. control group, #p < 0.05 vs. E2 group ).

Article Snippet: The antibodies used during Western blots included rabbit anti-human ERα from Proteintech, rabbit anti-human ERβ (1:500) from Proteintech, mouse anti-human MMP-1(1:400) from Santa Cruz, mouse anti-human MMP-2(1:400) from Santa Cruz, rabbit anti-human MMP-9 (1:500) from Proteintech, rabbit anti-human p38MAPK(1:500)/p-p38MAPK(1:500) and rabbit anti-human tAkt (1:500)/pAkt(1:500) from Bioworld Technology.

Techniques: Injection, Expressing, Western Blot