19803t Search Results


c haemolyticum dsm 19808t  (ATCC)
91
ATCC c haemolyticum dsm 19808t
C Haemolyticum Dsm 19808t, supplied by ATCC, 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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naquotinib  (MedChemExpress)
90
MedChemExpress naquotinib
Naquotinib, supplied by MedChemExpress, 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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non p β catenin  (Cell Signaling Technology Inc)
96
Cell Signaling Technology Inc non p β catenin
Figure 6. ISO suppressed migration and invasion <t>through</t> <t>NEDD9/β-Catenin</t> signaling. (A) A549 cells were treated with 40 µM ISO for 24 h. The whole-cell lysates were collected for immunoblotting analysis. (B) A549 cells with and without stable expression of NEDD9 treated with 40 µM ISO for 24 h were subjected to immunoblotting analysis. The band intensity was evaluated using ImageJ (version 1.53m), followed by normalization. (C,D) A549 cells with and without stable expression of NEDD9 in combination with ISO treatment (40 µM) were subjected to a transwell invasion and migration assay. After 48 h, cells were fixed and stained. Images were captured using an Olympus microscope. Invaded (C) and migrated cells (D) were counted and recorded. * and #, p < 0.05, compared to the cells without stable expression of NEDD9 and the cells with stable expression of NEDD9 but without ISO treatment, respectively.
Non P β Catenin, supplied by Cell Signaling Technology Inc, 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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anti-insulin novus nbp1-19803 antibody  (Novus Biologicals)
90
Novus Biologicals anti-insulin novus nbp1-19803 antibody
Figure 6. ISO suppressed migration and invasion <t>through</t> <t>NEDD9/β-Catenin</t> signaling. (A) A549 cells were treated with 40 µM ISO for 24 h. The whole-cell lysates were collected for immunoblotting analysis. (B) A549 cells with and without stable expression of NEDD9 treated with 40 µM ISO for 24 h were subjected to immunoblotting analysis. The band intensity was evaluated using ImageJ (version 1.53m), followed by normalization. (C,D) A549 cells with and without stable expression of NEDD9 in combination with ISO treatment (40 µM) were subjected to a transwell invasion and migration assay. After 48 h, cells were fixed and stained. Images were captured using an Olympus microscope. Invaded (C) and migrated cells (D) were counted and recorded. * and #, p < 0.05, compared to the cells without stable expression of NEDD9 and the cells with stable expression of NEDD9 but without ISO treatment, respectively.
Anti Insulin Novus Nbp1 19803 Antibody, supplied by Novus Biologicals, 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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Average 90 stars, based on 1 article reviews
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ig-23670  (Olon Ricerca Bioscience)
90
Olon Ricerca Bioscience ig-23670
Figure 6. ISO suppressed migration and invasion <t>through</t> <t>NEDD9/β-Catenin</t> signaling. (A) A549 cells were treated with 40 µM ISO for 24 h. The whole-cell lysates were collected for immunoblotting analysis. (B) A549 cells with and without stable expression of NEDD9 treated with 40 µM ISO for 24 h were subjected to immunoblotting analysis. The band intensity was evaluated using ImageJ (version 1.53m), followed by normalization. (C,D) A549 cells with and without stable expression of NEDD9 in combination with ISO treatment (40 µM) were subjected to a transwell invasion and migration assay. After 48 h, cells were fixed and stained. Images were captured using an Olympus microscope. Invaded (C) and migrated cells (D) were counted and recorded. * and #, p < 0.05, compared to the cells without stable expression of NEDD9 and the cells with stable expression of NEDD9 but without ISO treatment, respectively.
Ig 23670, supplied by Olon Ricerca Bioscience, 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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Average 90 stars, based on 1 article reviews
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m75054 92 0 pasteurella testudinis  (ATCC)
90
ATCC m75054 92 0 pasteurella testudinis
Figure 6. ISO suppressed migration and invasion <t>through</t> <t>NEDD9/β-Catenin</t> signaling. (A) A549 cells were treated with 40 µM ISO for 24 h. The whole-cell lysates were collected for immunoblotting analysis. (B) A549 cells with and without stable expression of NEDD9 treated with 40 µM ISO for 24 h were subjected to immunoblotting analysis. The band intensity was evaluated using ImageJ (version 1.53m), followed by normalization. (C,D) A549 cells with and without stable expression of NEDD9 in combination with ISO treatment (40 µM) were subjected to a transwell invasion and migration assay. After 48 h, cells were fixed and stained. Images were captured using an Olympus microscope. Invaded (C) and migrated cells (D) were counted and recorded. * and #, p < 0.05, compared to the cells without stable expression of NEDD9 and the cells with stable expression of NEDD9 but without ISO treatment, respectively.
M75054 92 0 Pasteurella Testudinis, supplied by ATCC, 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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9 00e  (ATCC)
94
ATCC 9 00e
Figure 6. ISO suppressed migration and invasion <t>through</t> <t>NEDD9/β-Catenin</t> signaling. (A) A549 cells were treated with 40 µM ISO for 24 h. The whole-cell lysates were collected for immunoblotting analysis. (B) A549 cells with and without stable expression of NEDD9 treated with 40 µM ISO for 24 h were subjected to immunoblotting analysis. The band intensity was evaluated using ImageJ (version 1.53m), followed by normalization. (C,D) A549 cells with and without stable expression of NEDD9 in combination with ISO treatment (40 µM) were subjected to a transwell invasion and migration assay. After 48 h, cells were fixed and stained. Images were captured using an Olympus microscope. Invaded (C) and migrated cells (D) were counted and recorded. * and #, p < 0.05, compared to the cells without stable expression of NEDD9 and the cells with stable expression of NEDD9 but without ISO treatment, respectively.
9 00e, 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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Average 94 stars, based on 1 article reviews
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rrid addgene 198035 and rrid addgene 208874  (Addgene inc)
88
Addgene inc rrid addgene 198035 and rrid addgene 208874
Figure 6. ISO suppressed migration and invasion <t>through</t> <t>NEDD9/β-Catenin</t> signaling. (A) A549 cells were treated with 40 µM ISO for 24 h. The whole-cell lysates were collected for immunoblotting analysis. (B) A549 cells with and without stable expression of NEDD9 treated with 40 µM ISO for 24 h were subjected to immunoblotting analysis. The band intensity was evaluated using ImageJ (version 1.53m), followed by normalization. (C,D) A549 cells with and without stable expression of NEDD9 in combination with ISO treatment (40 µM) were subjected to a transwell invasion and migration assay. After 48 h, cells were fixed and stained. Images were captured using an Olympus microscope. Invaded (C) and migrated cells (D) were counted and recorded. * and #, p < 0.05, compared to the cells without stable expression of NEDD9 and the cells with stable expression of NEDD9 but without ISO treatment, respectively.
Rrid Addgene 198035 And Rrid Addgene 208874, supplied by Addgene inc, 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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Average 88 stars, based on 1 article reviews
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molecular endocrinology, research and development  (Esoterix Genetic Laboratories)
90
Esoterix Genetic Laboratories molecular endocrinology, research and development
Figure 6. ISO suppressed migration and invasion <t>through</t> <t>NEDD9/β-Catenin</t> signaling. (A) A549 cells were treated with 40 µM ISO for 24 h. The whole-cell lysates were collected for immunoblotting analysis. (B) A549 cells with and without stable expression of NEDD9 treated with 40 µM ISO for 24 h were subjected to immunoblotting analysis. The band intensity was evaluated using ImageJ (version 1.53m), followed by normalization. (C,D) A549 cells with and without stable expression of NEDD9 in combination with ISO treatment (40 µM) were subjected to a transwell invasion and migration assay. After 48 h, cells were fixed and stained. Images were captured using an Olympus microscope. Invaded (C) and migrated cells (D) were counted and recorded. * and #, p < 0.05, compared to the cells without stable expression of NEDD9 and the cells with stable expression of NEDD9 but without ISO treatment, respectively.
Molecular Endocrinology, Research And Development, supplied by Esoterix Genetic Laboratories, 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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Average 90 stars, based on 1 article reviews
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s. salsuginis dsm 19800t  (DSMZ)
90
DSMZ s. salsuginis dsm 19800t
Figure 6. ISO suppressed migration and invasion <t>through</t> <t>NEDD9/β-Catenin</t> signaling. (A) A549 cells were treated with 40 µM ISO for 24 h. The whole-cell lysates were collected for immunoblotting analysis. (B) A549 cells with and without stable expression of NEDD9 treated with 40 µM ISO for 24 h were subjected to immunoblotting analysis. The band intensity was evaluated using ImageJ (version 1.53m), followed by normalization. (C,D) A549 cells with and without stable expression of NEDD9 in combination with ISO treatment (40 µM) were subjected to a transwell invasion and migration assay. After 48 h, cells were fixed and stained. Images were captured using an Olympus microscope. Invaded (C) and migrated cells (D) were counted and recorded. * and #, p < 0.05, compared to the cells without stable expression of NEDD9 and the cells with stable expression of NEDD9 but without ISO treatment, respectively.
S. Salsuginis Dsm 19800t, supplied by DSMZ, 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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epi-il lumination microscopy dino-lite am7915mzt  (Dunwell Tech Inc)
90
Dunwell Tech Inc epi-il lumination microscopy dino-lite am7915mzt
Figure 6. ISO suppressed migration and invasion <t>through</t> <t>NEDD9/β-Catenin</t> signaling. (A) A549 cells were treated with 40 µM ISO for 24 h. The whole-cell lysates were collected for immunoblotting analysis. (B) A549 cells with and without stable expression of NEDD9 treated with 40 µM ISO for 24 h were subjected to immunoblotting analysis. The band intensity was evaluated using ImageJ (version 1.53m), followed by normalization. (C,D) A549 cells with and without stable expression of NEDD9 in combination with ISO treatment (40 µM) were subjected to a transwell invasion and migration assay. After 48 h, cells were fixed and stained. Images were captured using an Olympus microscope. Invaded (C) and migrated cells (D) were counted and recorded. * and #, p < 0.05, compared to the cells without stable expression of NEDD9 and the cells with stable expression of NEDD9 but without ISO treatment, respectively.
Epi Il Lumination Microscopy Dino Lite Am7915mzt, supplied by Dunwell Tech Inc, 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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atcc 19803  (ATCC)
94
ATCC atcc 19803
Figure 6. ISO suppressed migration and invasion <t>through</t> <t>NEDD9/β-Catenin</t> signaling. (A) A549 cells were treated with 40 µM ISO for 24 h. The whole-cell lysates were collected for immunoblotting analysis. (B) A549 cells with and without stable expression of NEDD9 treated with 40 µM ISO for 24 h were subjected to immunoblotting analysis. The band intensity was evaluated using ImageJ (version 1.53m), followed by normalization. (C,D) A549 cells with and without stable expression of NEDD9 in combination with ISO treatment (40 µM) were subjected to a transwell invasion and migration assay. After 48 h, cells were fixed and stained. Images were captured using an Olympus microscope. Invaded (C) and migrated cells (D) were counted and recorded. * and #, p < 0.05, compared to the cells without stable expression of NEDD9 and the cells with stable expression of NEDD9 but without ISO treatment, respectively.
Atcc 19803, 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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Average 94 stars, based on 1 article reviews
atcc 19803 - by Bioz Stars, 2026-02
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Image Search Results


Figure 6. ISO suppressed migration and invasion through NEDD9/β-Catenin signaling. (A) A549 cells were treated with 40 µM ISO for 24 h. The whole-cell lysates were collected for immunoblotting analysis. (B) A549 cells with and without stable expression of NEDD9 treated with 40 µM ISO for 24 h were subjected to immunoblotting analysis. The band intensity was evaluated using ImageJ (version 1.53m), followed by normalization. (C,D) A549 cells with and without stable expression of NEDD9 in combination with ISO treatment (40 µM) were subjected to a transwell invasion and migration assay. After 48 h, cells were fixed and stained. Images were captured using an Olympus microscope. Invaded (C) and migrated cells (D) were counted and recorded. * and #, p < 0.05, compared to the cells without stable expression of NEDD9 and the cells with stable expression of NEDD9 but without ISO treatment, respectively.

Journal: International journal of molecular sciences

Article Title: Isorhapontigenin Inhibits Cell Growth, Angiogenesis, Migration, and Invasion of Non-Small-Cell Lung Cancer Cells Through NEDD9 Signaling.

doi: 10.3390/ijms26094207

Figure Lengend Snippet: Figure 6. ISO suppressed migration and invasion through NEDD9/β-Catenin signaling. (A) A549 cells were treated with 40 µM ISO for 24 h. The whole-cell lysates were collected for immunoblotting analysis. (B) A549 cells with and without stable expression of NEDD9 treated with 40 µM ISO for 24 h were subjected to immunoblotting analysis. The band intensity was evaluated using ImageJ (version 1.53m), followed by normalization. (C,D) A549 cells with and without stable expression of NEDD9 in combination with ISO treatment (40 µM) were subjected to a transwell invasion and migration assay. After 48 h, cells were fixed and stained. Images were captured using an Olympus microscope. Invaded (C) and migrated cells (D) were counted and recorded. * and #, p < 0.05, compared to the cells without stable expression of NEDD9 and the cells with stable expression of NEDD9 but without ISO treatment, respectively.

Article Snippet: Primary antibodies against NEDD9 (Cat# 4044), non-p-β-Catenin (Cat# 19807), β-Catenin (Cat# 9582), and secondary antibodies against mice (Cat# 7056) and rabbits (Cat# 7054) were purchased from Cell Signaling Inc. (Beverly, MA, USA).

Techniques: Migration, Western Blot, Expressing, Staining, Microscopy