p-axl antibodies (y702) Search Results


95
Cell Signaling Technology Inc anti paxl y702
Anti Paxl Y702, 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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Santa Cruz Biotechnology anti aldh1a1
Anti Aldh1a1, supplied by Santa Cruz Biotechnology, 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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Cell Signaling Technology Inc akt
Akt, supplied by Cell Signaling Technology Inc, 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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97
Cell Signaling Technology Inc e cadherin
Figure 2 Axl overexpression induces EMTand promotes the invasion and proliferation of GC cells. BGC-823 and SGC-7901 cells were transfected with Axl overexpressing plasmid. (A) The expression of Axl mRNA in GC cells was determined RT-PCR assay. (B) The expression of Axl, <t>E-cadherin,</t> and vimentin in GC cells were measured by Western blot assay. Representative blots are shown and GAPDH serve as a loading control. (C) The mRNA expression of E-cadherin (CDH1) and vimentin (VIM) expression levels were examined by RT-PCR assay. (D) Transwell invasion assay was used to detect cell invasion capacities. Representative images and quantification of invaded cells are shown. Scar bar, 200 μm. (E) EdU cell proliferation assay and (F) CCK-8 assay were performed to examine GC cell proliferation. Representative images and quantification of EdU-positive cells are shown. Scar bar, 100 μm. Data are shown as mean ± SEM, n = 3. **P < 0.01 and ***P < 0.001 compared with the vector groups.
E Cadherin, supplied by Cell Signaling Technology Inc, 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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Average 97 stars, based on 1 article reviews
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Cell Signaling Technology Inc anti α tubulin
Figure 2 Axl overexpression induces EMTand promotes the invasion and proliferation of GC cells. BGC-823 and SGC-7901 cells were transfected with Axl overexpressing plasmid. (A) The expression of Axl mRNA in GC cells was determined RT-PCR assay. (B) The expression of Axl, <t>E-cadherin,</t> and vimentin in GC cells were measured by Western blot assay. Representative blots are shown and GAPDH serve as a loading control. (C) The mRNA expression of E-cadherin (CDH1) and vimentin (VIM) expression levels were examined by RT-PCR assay. (D) Transwell invasion assay was used to detect cell invasion capacities. Representative images and quantification of invaded cells are shown. Scar bar, 200 μm. (E) EdU cell proliferation assay and (F) CCK-8 assay were performed to examine GC cell proliferation. Representative images and quantification of EdU-positive cells are shown. Scar bar, 100 μm. Data are shown as mean ± SEM, n = 3. **P < 0.01 and ***P < 0.001 compared with the vector groups.
Anti α Tubulin, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/p-axl+antibodies+(y702)/alpha-Tubulin+Antibody/pmc07016176-194-30-31
Average 97 stars, based on 1 article reviews
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96
Cell Signaling Technology Inc 8661s
Figure 2 Axl overexpression induces EMTand promotes the invasion and proliferation of GC cells. BGC-823 and SGC-7901 cells were transfected with Axl overexpressing plasmid. (A) The expression of Axl mRNA in GC cells was determined RT-PCR assay. (B) The expression of Axl, <t>E-cadherin,</t> and vimentin in GC cells were measured by Western blot assay. Representative blots are shown and GAPDH serve as a loading control. (C) The mRNA expression of E-cadherin (CDH1) and vimentin (VIM) expression levels were examined by RT-PCR assay. (D) Transwell invasion assay was used to detect cell invasion capacities. Representative images and quantification of invaded cells are shown. Scar bar, 200 μm. (E) EdU cell proliferation assay and (F) CCK-8 assay were performed to examine GC cell proliferation. Representative images and quantification of EdU-positive cells are shown. Scar bar, 100 μm. Data are shown as mean ± SEM, n = 3. **P < 0.01 and ***P < 0.001 compared with the vector groups.
8661s, 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
https://www.bioz.com/product/p-axl+antibodies+(y702)/Axl+Rabbit+mAb/bio_rxiv__2025__02__21__639478-55-5-19
Average 96 stars, based on 1 article reviews
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93
Santa Cruz Biotechnology anti p130cas mouse
Figure 2 Axl overexpression induces EMTand promotes the invasion and proliferation of GC cells. BGC-823 and SGC-7901 cells were transfected with Axl overexpressing plasmid. (A) The expression of Axl mRNA in GC cells was determined RT-PCR assay. (B) The expression of Axl, <t>E-cadherin,</t> and vimentin in GC cells were measured by Western blot assay. Representative blots are shown and GAPDH serve as a loading control. (C) The mRNA expression of E-cadherin (CDH1) and vimentin (VIM) expression levels were examined by RT-PCR assay. (D) Transwell invasion assay was used to detect cell invasion capacities. Representative images and quantification of invaded cells are shown. Scar bar, 200 μm. (E) EdU cell proliferation assay and (F) CCK-8 assay were performed to examine GC cell proliferation. Representative images and quantification of EdU-positive cells are shown. Scar bar, 100 μm. Data are shown as mean ± SEM, n = 3. **P < 0.01 and ***P < 0.001 compared with the vector groups.
Anti P130cas Mouse, supplied by Santa Cruz Biotechnology, 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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Average 93 stars, based on 1 article reviews
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96
Santa Cruz Biotechnology anti vimentin
Figure 2 Axl overexpression induces EMTand promotes the invasion and proliferation of GC cells. BGC-823 and SGC-7901 cells were transfected with Axl overexpressing plasmid. (A) The expression of Axl mRNA in GC cells was determined RT-PCR assay. (B) The expression of Axl, <t>E-cadherin,</t> and vimentin in GC cells were measured by Western blot assay. Representative blots are shown and GAPDH serve as a loading control. (C) The mRNA expression of E-cadherin (CDH1) and vimentin (VIM) expression levels were examined by RT-PCR assay. (D) Transwell invasion assay was used to detect cell invasion capacities. Representative images and quantification of invaded cells are shown. Scar bar, 200 μm. (E) EdU cell proliferation assay and (F) CCK-8 assay were performed to examine GC cell proliferation. Representative images and quantification of EdU-positive cells are shown. Scar bar, 100 μm. Data are shown as mean ± SEM, n = 3. **P < 0.01 and ***P < 0.001 compared with the vector groups.
Anti Vimentin, 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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Average 96 stars, based on 1 article reviews
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93
Santa Cruz Biotechnology anti gas6
Figure 2 Axl overexpression induces EMTand promotes the invasion and proliferation of GC cells. BGC-823 and SGC-7901 cells were transfected with Axl overexpressing plasmid. (A) The expression of Axl mRNA in GC cells was determined RT-PCR assay. (B) The expression of Axl, <t>E-cadherin,</t> and vimentin in GC cells were measured by Western blot assay. Representative blots are shown and GAPDH serve as a loading control. (C) The mRNA expression of E-cadherin (CDH1) and vimentin (VIM) expression levels were examined by RT-PCR assay. (D) Transwell invasion assay was used to detect cell invasion capacities. Representative images and quantification of invaded cells are shown. Scar bar, 200 μm. (E) EdU cell proliferation assay and (F) CCK-8 assay were performed to examine GC cell proliferation. Representative images and quantification of EdU-positive cells are shown. Scar bar, 100 μm. Data are shown as mean ± SEM, n = 3. **P < 0.01 and ***P < 0.001 compared with the vector groups.
Anti Gas6, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/p-axl+antibodies+(y702)/Gas6+Antibody/pmc05736582-191-26-33
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93
Cell Signaling Technology Inc anti p tyrosine
Figure 2 Axl overexpression induces EMTand promotes the invasion and proliferation of GC cells. BGC-823 and SGC-7901 cells were transfected with Axl overexpressing plasmid. (A) The expression of Axl mRNA in GC cells was determined RT-PCR assay. (B) The expression of Axl, <t>E-cadherin,</t> and vimentin in GC cells were measured by Western blot assay. Representative blots are shown and GAPDH serve as a loading control. (C) The mRNA expression of E-cadherin (CDH1) and vimentin (VIM) expression levels were examined by RT-PCR assay. (D) Transwell invasion assay was used to detect cell invasion capacities. Representative images and quantification of invaded cells are shown. Scar bar, 200 μm. (E) EdU cell proliferation assay and (F) CCK-8 assay were performed to examine GC cell proliferation. Representative images and quantification of EdU-positive cells are shown. Scar bar, 100 μm. Data are shown as mean ± SEM, n = 3. **P < 0.01 and ***P < 0.001 compared with the vector groups.
Anti P Tyrosine, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/p-axl+antibodies+(y702)/Phospho-Tyrosine+Mouse+mAb/pm26356564-183-11-17
Average 93 stars, based on 1 article reviews
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96
Cell Signaling Technology Inc mek1 2
Figure 2 Axl overexpression induces EMTand promotes the invasion and proliferation of GC cells. BGC-823 and SGC-7901 cells were transfected with Axl overexpressing plasmid. (A) The expression of Axl mRNA in GC cells was determined RT-PCR assay. (B) The expression of Axl, <t>E-cadherin,</t> and vimentin in GC cells were measured by Western blot assay. Representative blots are shown and GAPDH serve as a loading control. (C) The mRNA expression of E-cadherin (CDH1) and vimentin (VIM) expression levels were examined by RT-PCR assay. (D) Transwell invasion assay was used to detect cell invasion capacities. Representative images and quantification of invaded cells are shown. Scar bar, 200 μm. (E) EdU cell proliferation assay and (F) CCK-8 assay were performed to examine GC cell proliferation. Representative images and quantification of EdU-positive cells are shown. Scar bar, 100 μm. Data are shown as mean ± SEM, n = 3. **P < 0.01 and ***P < 0.001 compared with the vector groups.
Mek1 2, 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
https://www.bioz.com/product/p-axl+antibodies+(y702)/MEK1%2F2+Antibody/pmc07717506-52-17-26
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96
Santa Cruz Biotechnology py99 sc 7020
Figure 2 Axl overexpression induces EMTand promotes the invasion and proliferation of GC cells. BGC-823 and SGC-7901 cells were transfected with Axl overexpressing plasmid. (A) The expression of Axl mRNA in GC cells was determined RT-PCR assay. (B) The expression of Axl, <t>E-cadherin,</t> and vimentin in GC cells were measured by Western blot assay. Representative blots are shown and GAPDH serve as a loading control. (C) The mRNA expression of E-cadherin (CDH1) and vimentin (VIM) expression levels were examined by RT-PCR assay. (D) Transwell invasion assay was used to detect cell invasion capacities. Representative images and quantification of invaded cells are shown. Scar bar, 200 μm. (E) EdU cell proliferation assay and (F) CCK-8 assay were performed to examine GC cell proliferation. Representative images and quantification of EdU-positive cells are shown. Scar bar, 100 μm. Data are shown as mean ± SEM, n = 3. **P < 0.01 and ***P < 0.001 compared with the vector groups.
Py99 Sc 7020, 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


Figure 2 Axl overexpression induces EMTand promotes the invasion and proliferation of GC cells. BGC-823 and SGC-7901 cells were transfected with Axl overexpressing plasmid. (A) The expression of Axl mRNA in GC cells was determined RT-PCR assay. (B) The expression of Axl, E-cadherin, and vimentin in GC cells were measured by Western blot assay. Representative blots are shown and GAPDH serve as a loading control. (C) The mRNA expression of E-cadherin (CDH1) and vimentin (VIM) expression levels were examined by RT-PCR assay. (D) Transwell invasion assay was used to detect cell invasion capacities. Representative images and quantification of invaded cells are shown. Scar bar, 200 μm. (E) EdU cell proliferation assay and (F) CCK-8 assay were performed to examine GC cell proliferation. Representative images and quantification of EdU-positive cells are shown. Scar bar, 100 μm. Data are shown as mean ± SEM, n = 3. **P < 0.01 and ***P < 0.001 compared with the vector groups.

Journal: OncoTargets and Therapy

Article Title:

Implications of the Receptor Tyrosine Kinase Axl in Gastric Cancer Progression

doi: 10.2147/ott.s257606

Figure Lengend Snippet: Figure 2 Axl overexpression induces EMTand promotes the invasion and proliferation of GC cells. BGC-823 and SGC-7901 cells were transfected with Axl overexpressing plasmid. (A) The expression of Axl mRNA in GC cells was determined RT-PCR assay. (B) The expression of Axl, E-cadherin, and vimentin in GC cells were measured by Western blot assay. Representative blots are shown and GAPDH serve as a loading control. (C) The mRNA expression of E-cadherin (CDH1) and vimentin (VIM) expression levels were examined by RT-PCR assay. (D) Transwell invasion assay was used to detect cell invasion capacities. Representative images and quantification of invaded cells are shown. Scar bar, 200 μm. (E) EdU cell proliferation assay and (F) CCK-8 assay were performed to examine GC cell proliferation. Representative images and quantification of EdU-positive cells are shown. Scar bar, 100 μm. Data are shown as mean ± SEM, n = 3. **P < 0.01 and ***P < 0.001 compared with the vector groups.

Article Snippet: Antibodies against Gas6, Axl, p-Axl (Y702), E-cadherin, vimentin, ZEB1 and GAPDH were obtained from Cell Signaling Technology (Danvers, MA, USA).

Techniques: Over Expression, Transfection, Plasmid Preparation, Expressing, Reverse Transcription Polymerase Chain Reaction, Western Blot, Control, Transwell Invasion Assay, Proliferation Assay, CCK-8 Assay

Figure 3 Silencing Axl inhibits EMT and suppresses the invasion and proliferation of GC cells. BGC-823 and SGC-7901 cells were transfected with Axl specific siRNA. (A) The expression of Axl in cells were determined by RT-PCR assay. (B) The expression of Axl, E-cadherin, and vimentin in GC cells were detected by Western blot assay. Representative blots are shown and GAPDH serve as a loading control. (C) RT-PCR assay for the expression of CDH1 and VIM expression levels in GC cells. (D) The invasion of GC cells was detected by Transwell invasion assay. Representative images and quantification of invaded cells are shown. Scar bar, 200 μm. (E and F) The proliferation of GC cells was examined by (E) EdU cell proliferation assay and (F) CCK-8 assay. Scar bar, 100 μm. Representative images and quantification of EdU-positive cells are shown. Data are shown as mean ± SEM, n = 3. *P < 0.05, **P < 0.01, and ***P < 0.001 compared with the NC siRNA groups.

Journal: OncoTargets and Therapy

Article Title:

Implications of the Receptor Tyrosine Kinase Axl in Gastric Cancer Progression

doi: 10.2147/ott.s257606

Figure Lengend Snippet: Figure 3 Silencing Axl inhibits EMT and suppresses the invasion and proliferation of GC cells. BGC-823 and SGC-7901 cells were transfected with Axl specific siRNA. (A) The expression of Axl in cells were determined by RT-PCR assay. (B) The expression of Axl, E-cadherin, and vimentin in GC cells were detected by Western blot assay. Representative blots are shown and GAPDH serve as a loading control. (C) RT-PCR assay for the expression of CDH1 and VIM expression levels in GC cells. (D) The invasion of GC cells was detected by Transwell invasion assay. Representative images and quantification of invaded cells are shown. Scar bar, 200 μm. (E and F) The proliferation of GC cells was examined by (E) EdU cell proliferation assay and (F) CCK-8 assay. Scar bar, 100 μm. Representative images and quantification of EdU-positive cells are shown. Data are shown as mean ± SEM, n = 3. *P < 0.05, **P < 0.01, and ***P < 0.001 compared with the NC siRNA groups.

Article Snippet: Antibodies against Gas6, Axl, p-Axl (Y702), E-cadherin, vimentin, ZEB1 and GAPDH were obtained from Cell Signaling Technology (Danvers, MA, USA).

Techniques: Transfection, Expressing, Reverse Transcription Polymerase Chain Reaction, Western Blot, Control, Transwell Invasion Assay, Proliferation Assay, CCK-8 Assay

Figure 5 The knockdown of ZEB1 impairs EMT and blocks the invasion and proliferation in GC cells. BGC-823 and SGC7901 cells were transfected with ZEB1 specific siRNA. (A) RT-PCR assay was used to examine ZEB1 level in GC cells. (B) The expression of ZEB1, E-cadherin and vimentin in GC cells were detected by Western blot assay. Representative blots are shown and GAPDH serve as a loading control. (C) CDH1 and VIM expression levels in GC cells were determined by RT-PCR assay. (D) Transwell invasion assay was performed to detect GC cell invasion. Representative images and quantification of invaded cells are shown. Scar bar, 200 μm. (E) Cell proliferation was examined by EdU cell proliferation assay. Representative images and quantification of EdU-positive cells are shown. Scar bar, 100 μm. Data are shown as mean ± SEM, n = 3. **P < 0.01, and ***P < 0.001 compared with the NC siRNA groups.

Journal: OncoTargets and Therapy

Article Title:

Implications of the Receptor Tyrosine Kinase Axl in Gastric Cancer Progression

doi: 10.2147/ott.s257606

Figure Lengend Snippet: Figure 5 The knockdown of ZEB1 impairs EMT and blocks the invasion and proliferation in GC cells. BGC-823 and SGC7901 cells were transfected with ZEB1 specific siRNA. (A) RT-PCR assay was used to examine ZEB1 level in GC cells. (B) The expression of ZEB1, E-cadherin and vimentin in GC cells were detected by Western blot assay. Representative blots are shown and GAPDH serve as a loading control. (C) CDH1 and VIM expression levels in GC cells were determined by RT-PCR assay. (D) Transwell invasion assay was performed to detect GC cell invasion. Representative images and quantification of invaded cells are shown. Scar bar, 200 μm. (E) Cell proliferation was examined by EdU cell proliferation assay. Representative images and quantification of EdU-positive cells are shown. Scar bar, 100 μm. Data are shown as mean ± SEM, n = 3. **P < 0.01, and ***P < 0.001 compared with the NC siRNA groups.

Article Snippet: Antibodies against Gas6, Axl, p-Axl (Y702), E-cadherin, vimentin, ZEB1 and GAPDH were obtained from Cell Signaling Technology (Danvers, MA, USA).

Techniques: Knockdown, Transfection, Reverse Transcription Polymerase Chain Reaction, Expressing, Western Blot, Control, Transwell Invasion Assay, Proliferation Assay