p cynomolgi atcc 30149 Search Results


p cynomolgi atcc 30149  (ATCC)
92
ATCC p cynomolgi atcc 30149
P Cynomolgi Atcc 30149, supplied by ATCC, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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plasmodium cynomolgi  (ATCC)
91
ATCC plasmodium cynomolgi
Plasmodium Cynomolgi, 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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sappα  (Addgene inc)
88
Addgene inc sappα
Expression <t>of</t> <t>APP</t> and its proteolytic product in breast cancer cell lines. (A) Immunoblot analysis using an antibody against APP N-terminal (clone 22C11) showing differential expression of APP on breast cancer cell lines BT-549, MDA-MB231, MCF7, MDA-MB468, SK-BR-3 and ZR-75-1. α-tubulin was used as a control. Densitometric analysis of APP expression from triplicate experiments was shown at the lower panel. (mean ± SD; n = 3). (B) Conditioned medium from cell line culture was examined using antibodies specific for <t>sAPPα</t> and sAPPβ, in addition to clone 22C11. Secretion of sAPPα, but not sAPPβ into cell culture supernatant can be detected. All experiments were performed at least three times.
Sappα, 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
https://www.bioz.com/product/p+cynomolgi+atcc+30149/pCAX+APPs-751-alpha+(Plasmid+%2330149)/pmc06306343-89-8-13
Average 88 stars, based on 1 article reviews
sappα - by Bioz Stars, 2026-11
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ammonium chloride  (Chem Impex International)
95
Chem Impex International ammonium chloride
Expression <t>of</t> <t>APP</t> and its proteolytic product in breast cancer cell lines. (A) Immunoblot analysis using an antibody against APP N-terminal (clone 22C11) showing differential expression of APP on breast cancer cell lines BT-549, MDA-MB231, MCF7, MDA-MB468, SK-BR-3 and ZR-75-1. α-tubulin was used as a control. Densitometric analysis of APP expression from triplicate experiments was shown at the lower panel. (mean ± SD; n = 3). (B) Conditioned medium from cell line culture was examined using antibodies specific for <t>sAPPα</t> and sAPPβ, in addition to clone 22C11. Secretion of sAPPα, but not sAPPβ into cell culture supernatant can be detected. All experiments were performed at least three times.
Ammonium Chloride, 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
https://www.bioz.com/product/p+cynomolgi+atcc+30149/Ammonium+chloride/custom%4030149%40us07053110
Average 95 stars, based on 1 article reviews
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rep. uicd-30149  (Lawrence Livermore National Security LLC)
90
Lawrence Livermore National Security LLC rep. uicd-30149
Expression <t>of</t> <t>APP</t> and its proteolytic product in breast cancer cell lines. (A) Immunoblot analysis using an antibody against APP N-terminal (clone 22C11) showing differential expression of APP on breast cancer cell lines BT-549, MDA-MB231, MCF7, MDA-MB468, SK-BR-3 and ZR-75-1. α-tubulin was used as a control. Densitometric analysis of APP expression from triplicate experiments was shown at the lower panel. (mean ± SD; n = 3). (B) Conditioned medium from cell line culture was examined using antibodies specific for <t>sAPPα</t> and sAPPβ, in addition to clone 22C11. Secretion of sAPPα, but not sAPPβ into cell culture supernatant can be detected. All experiments were performed at least three times.
Rep. Uicd 30149, supplied by Lawrence Livermore National Security LLC, 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/product/p+cynomolgi+atcc+30149/rep++uicd+30149/10__1145_slash_4078__4079-1264-0-2
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stroop color word test  (Stoelting inc)
92
Stoelting inc stroop color word test
Expression <t>of</t> <t>APP</t> and its proteolytic product in breast cancer cell lines. (A) Immunoblot analysis using an antibody against APP N-terminal (clone 22C11) showing differential expression of APP on breast cancer cell lines BT-549, MDA-MB231, MCF7, MDA-MB468, SK-BR-3 and ZR-75-1. α-tubulin was used as a control. Densitometric analysis of APP expression from triplicate experiments was shown at the lower panel. (mean ± SD; n = 3). (B) Conditioned medium from cell line culture was examined using antibodies specific for <t>sAPPα</t> and sAPPβ, in addition to clone 22C11. Secretion of sAPPα, but not sAPPβ into cell culture supernatant can be detected. All experiments were performed at least three times.
Stroop Color Word Test, supplied by Stoelting inc, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/p+cynomolgi+atcc+30149/Stroop+Color+%26+Word+Test+Kit+for+Children/pm24352232-319-1-5
Average 92 stars, based on 1 article reviews
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Image Search Results


Expression of APP and its proteolytic product in breast cancer cell lines. (A) Immunoblot analysis using an antibody against APP N-terminal (clone 22C11) showing differential expression of APP on breast cancer cell lines BT-549, MDA-MB231, MCF7, MDA-MB468, SK-BR-3 and ZR-75-1. α-tubulin was used as a control. Densitometric analysis of APP expression from triplicate experiments was shown at the lower panel. (mean ± SD; n = 3). (B) Conditioned medium from cell line culture was examined using antibodies specific for sAPPα and sAPPβ, in addition to clone 22C11. Secretion of sAPPα, but not sAPPβ into cell culture supernatant can be detected. All experiments were performed at least three times.

Journal: EBioMedicine

Article Title: Proteolytic cleavage of amyloid precursor protein by ADAM10 mediates proliferation and migration in breast cancer

doi: 10.1016/j.ebiom.2018.11.012

Figure Lengend Snippet: Expression of APP and its proteolytic product in breast cancer cell lines. (A) Immunoblot analysis using an antibody against APP N-terminal (clone 22C11) showing differential expression of APP on breast cancer cell lines BT-549, MDA-MB231, MCF7, MDA-MB468, SK-BR-3 and ZR-75-1. α-tubulin was used as a control. Densitometric analysis of APP expression from triplicate experiments was shown at the lower panel. (mean ± SD; n = 3). (B) Conditioned medium from cell line culture was examined using antibodies specific for sAPPα and sAPPβ, in addition to clone 22C11. Secretion of sAPPα, but not sAPPβ into cell culture supernatant can be detected. All experiments were performed at least three times.

Article Snippet: The mammalian expression constructs for APP (pCAX-APP751) and sAPPα (pCAX-APPs-751-alpha) were obtained from Addgene.

Techniques: Expressing, Western Blot, Quantitative Proteomics, Control, Cell Culture

Overexpression of full length APP and sAPPα enhanced breast cancer proliferation and migration. (A) Expression of full length or sAPPα promoted proliferation in breast cancer cell line (MDA-MB231). MDA-MB231 was transfected with full length (FL), sAPP or control (CTR) construct and were seeded (1 × 10 3 ) in a 96 well plate. Western blotting analysis for APP expression after transfection was shown (insert). Cell proliferation was measured at day 4 by CCK8 assay. (mean ± SD; n = 3). Statistical analysis was performed using student t -test. ***p < 0.001. (B) APP overexpression enhanced migration of breast cancer. Cells transfected with different APP constructs (1 × 10 5 ) were seeded with 0.2 ml serum free medium in the upper chamber of Boyen chamber after overnight serum starvation. 0.5 ml medium supplemented with 10% FBS was added to the lower chamber. Migration was evaluated for 22 h. (mean ± SD; n = 3). Statistical analysis was performed using student t-test. ***p < 0.001. All experiments were performed at least three times.

Journal: EBioMedicine

Article Title: Proteolytic cleavage of amyloid precursor protein by ADAM10 mediates proliferation and migration in breast cancer

doi: 10.1016/j.ebiom.2018.11.012

Figure Lengend Snippet: Overexpression of full length APP and sAPPα enhanced breast cancer proliferation and migration. (A) Expression of full length or sAPPα promoted proliferation in breast cancer cell line (MDA-MB231). MDA-MB231 was transfected with full length (FL), sAPP or control (CTR) construct and were seeded (1 × 10 3 ) in a 96 well plate. Western blotting analysis for APP expression after transfection was shown (insert). Cell proliferation was measured at day 4 by CCK8 assay. (mean ± SD; n = 3). Statistical analysis was performed using student t -test. ***p < 0.001. (B) APP overexpression enhanced migration of breast cancer. Cells transfected with different APP constructs (1 × 10 5 ) were seeded with 0.2 ml serum free medium in the upper chamber of Boyen chamber after overnight serum starvation. 0.5 ml medium supplemented with 10% FBS was added to the lower chamber. Migration was evaluated for 22 h. (mean ± SD; n = 3). Statistical analysis was performed using student t-test. ***p < 0.001. All experiments were performed at least three times.

Article Snippet: The mammalian expression constructs for APP (pCAX-APP751) and sAPPα (pCAX-APPs-751-alpha) were obtained from Addgene.

Techniques: Over Expression, Migration, Expressing, Transfection, Control, Construct, Western Blot, CCK-8 Assay

ADAM10 and ADAM17 in APP processing of breast cancer cell lines. (A) Immunoblot analysis using antibodies against ADAM10 and ADAM17 showed the expression of both proteins in breast cancer cell lines (BT-549, MDA-MB231, MCF7, MDA-MB468, SK-BR-3 and ZR-75-1). β-actin was used as a control. Densitometric analysis of protein expression on the predominant form detected (pro-ADAM17 and mature ADAM10) from replicate experiments were shown at the lower panel. (mean ± SD; n = 3). (B) Knockdown of ADAM 10 but not ADAM17 showed reduced sAPP level in conditioned medium from cell line culture. Breast cancer cell line (MDA-MB231) was transfected with ADAM10 or ADAM17 siRNA showed a marked reduction in protein and mRNA expression. A decreased level of sAPP in the conditioned supernatant was found with ADAM10 but not ADAM17 knockdown. Densitometric analysis of APP and sAPP was shown at the right panel. (mean ± SD; n = 3). Statistical analysis was performed using student t -test. ***p < 0.001. All experiments were performed at least three times.

Journal: EBioMedicine

Article Title: Proteolytic cleavage of amyloid precursor protein by ADAM10 mediates proliferation and migration in breast cancer

doi: 10.1016/j.ebiom.2018.11.012

Figure Lengend Snippet: ADAM10 and ADAM17 in APP processing of breast cancer cell lines. (A) Immunoblot analysis using antibodies against ADAM10 and ADAM17 showed the expression of both proteins in breast cancer cell lines (BT-549, MDA-MB231, MCF7, MDA-MB468, SK-BR-3 and ZR-75-1). β-actin was used as a control. Densitometric analysis of protein expression on the predominant form detected (pro-ADAM17 and mature ADAM10) from replicate experiments were shown at the lower panel. (mean ± SD; n = 3). (B) Knockdown of ADAM 10 but not ADAM17 showed reduced sAPP level in conditioned medium from cell line culture. Breast cancer cell line (MDA-MB231) was transfected with ADAM10 or ADAM17 siRNA showed a marked reduction in protein and mRNA expression. A decreased level of sAPP in the conditioned supernatant was found with ADAM10 but not ADAM17 knockdown. Densitometric analysis of APP and sAPP was shown at the right panel. (mean ± SD; n = 3). Statistical analysis was performed using student t -test. ***p < 0.001. All experiments were performed at least three times.

Article Snippet: The mammalian expression constructs for APP (pCAX-APP751) and sAPPα (pCAX-APPs-751-alpha) were obtained from Addgene.

Techniques: Western Blot, Expressing, Control, Knockdown, Transfection