cosmx 1000 plex mrna panel Search Results


90
Cosmo Bio USA igf1
DEX inhibits the proliferation of BMSCs. (A) Cell viability of BMSCs measured by CCK8. BMSCs were treated with different concentrations of DEX. (B) Western blot assay was conducted for determining the expression of cell growth factor <t>IGF1.</t> (C) ELISA was conducted for the quantitative analysis of IGF1 expression changes over time. The concentration of DEX was set as 10 −7 mol/L. * p < .05, ** p < .01, *** p < .001
Igf1, supplied by Cosmo Bio USA, 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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90
Cosmo Oil Co Ltd swasol 1000
DEX inhibits the proliferation of BMSCs. (A) Cell viability of BMSCs measured by CCK8. BMSCs were treated with different concentrations of DEX. (B) Western blot assay was conducted for determining the expression of cell growth factor <t>IGF1.</t> (C) ELISA was conducted for the quantitative analysis of IGF1 expression changes over time. The concentration of DEX was set as 10 −7 mol/L. * p < .05, ** p < .01, *** p < .001
Swasol 1000, supplied by Cosmo Oil Co Ltd, 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/cosmx+1000+plex+mrna+panel/swasol+1000/us12240997-312-13-19
Average 90 stars, based on 1 article reviews
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90
Cosmo Bio USA anti cd81
Isolation of milk-derived exosomes (MDEs) and their uptake by different tumor and normal colon cells. Protein expression of <t>CD81</t> as a marker of exosomes and HSP70 as a negative control in MDEs ( a ). MDEs were analyzed by transmission electron microscopy using negative staining ( b ). Particle size distribution (by intensity) of isolated MDEs determined by DLS ( c ). Labeled milk exosomes isolated from human milk were incubated for 4 h with normal intestinal (CCD 841) or colon cancer (LS123) cells. Images were obtained by fluorescence microscope analysis ( d, e ). MiRNA-148a expression in CCD 841 and LS123 cells incubated with (EXO) or without (CONT) MDEs was analyzed by qRT-PCR ( f, g ). qRT-PCR results were calculated using the 2^(− ∆∆CT) method, and values were normalized against RNU6, *p < 0.05 t test
Anti Cd81, supplied by Cosmo Bio USA, 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/cosmx+1000+plex+mrna+panel/anti+cd81/pmc06767636-92-53-55
Average 90 stars, based on 1 article reviews
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Cosmo Bio USA antibody tip-ptdm01
Isolation of milk-derived exosomes (MDEs) and their uptake by different tumor and normal colon cells. Protein expression of <t>CD81</t> as a marker of exosomes and HSP70 as a negative control in MDEs ( a ). MDEs were analyzed by transmission electron microscopy using negative staining ( b ). Particle size distribution (by intensity) of isolated MDEs determined by DLS ( c ). Labeled milk exosomes isolated from human milk were incubated for 4 h with normal intestinal (CCD 841) or colon cancer (LS123) cells. Images were obtained by fluorescence microscope analysis ( d, e ). MiRNA-148a expression in CCD 841 and LS123 cells incubated with (EXO) or without (CONT) MDEs was analyzed by qRT-PCR ( f, g ). qRT-PCR results were calculated using the 2^(− ∆∆CT) method, and values were normalized against RNU6, *p < 0.05 t test
Antibody Tip Ptdm01, supplied by Cosmo Bio USA, 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/cosmx+1000+plex+mrna+panel/ptdp+43+antibody/pm33757575-32-91-97
Average 90 stars, based on 1 article reviews
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90
Cosmo Bio USA hrpconjugated anti-c-myc antibody
Isolation of milk-derived exosomes (MDEs) and their uptake by different tumor and normal colon cells. Protein expression of <t>CD81</t> as a marker of exosomes and HSP70 as a negative control in MDEs ( a ). MDEs were analyzed by transmission electron microscopy using negative staining ( b ). Particle size distribution (by intensity) of isolated MDEs determined by DLS ( c ). Labeled milk exosomes isolated from human milk were incubated for 4 h with normal intestinal (CCD 841) or colon cancer (LS123) cells. Images were obtained by fluorescence microscope analysis ( d, e ). MiRNA-148a expression in CCD 841 and LS123 cells incubated with (EXO) or without (CONT) MDEs was analyzed by qRT-PCR ( f, g ). qRT-PCR results were calculated using the 2^(− ∆∆CT) method, and values were normalized against RNU6, *p < 0.05 t test
Hrpconjugated Anti C Myc Antibody, supplied by Cosmo Bio USA, 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/cosmx+1000+plex+mrna+panel/hrpconjugated+anti+c+myc+antibody/pm38917513-82-49-52
Average 90 stars, based on 1 article reviews
hrpconjugated anti-c-myc antibody - by Bioz Stars, 2026-10
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95
Chem Impex International vwr extra pure
Isolation of milk-derived exosomes (MDEs) and their uptake by different tumor and normal colon cells. Protein expression of <t>CD81</t> as a marker of exosomes and HSP70 as a negative control in MDEs ( a ). MDEs were analyzed by transmission electron microscopy using negative staining ( b ). Particle size distribution (by intensity) of isolated MDEs determined by DLS ( c ). Labeled milk exosomes isolated from human milk were incubated for 4 h with normal intestinal (CCD 841) or colon cancer (LS123) cells. Images were obtained by fluorescence microscope analysis ( d, e ). MiRNA-148a expression in CCD 841 and LS123 cells incubated with (EXO) or without (CONT) MDEs was analyzed by qRT-PCR ( f, g ). qRT-PCR results were calculated using the 2^(− ∆∆CT) method, and values were normalized against RNU6, *p < 0.05 t test
Vwr Extra Pure, 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/cosmx+1000+plex+mrna+panel/Isopropyl+alcohol/pm20670021__ol101450u_si_001-34-28-32
Average 95 stars, based on 1 article reviews
vwr extra pure - by Bioz Stars, 2026-10
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90
Cosmo Bio USA anti-cpd
Isolation of milk-derived exosomes (MDEs) and their uptake by different tumor and normal colon cells. Protein expression of <t>CD81</t> as a marker of exosomes and HSP70 as a negative control in MDEs ( a ). MDEs were analyzed by transmission electron microscopy using negative staining ( b ). Particle size distribution (by intensity) of isolated MDEs determined by DLS ( c ). Labeled milk exosomes isolated from human milk were incubated for 4 h with normal intestinal (CCD 841) or colon cancer (LS123) cells. Images were obtained by fluorescence microscope analysis ( d, e ). MiRNA-148a expression in CCD 841 and LS123 cells incubated with (EXO) or without (CONT) MDEs was analyzed by qRT-PCR ( f, g ). qRT-PCR results were calculated using the 2^(− ∆∆CT) method, and values were normalized against RNU6, *p < 0.05 t test
Anti Cpd, supplied by Cosmo Bio USA, 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/cosmx+1000+plex+mrna+panel/anti+cpd+antibody+tdm+2/pm38745079-87-3-4
Average 90 stars, based on 1 article reviews
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96
Santa Cruz Biotechnology anti phospho erk1 2
Isolation of milk-derived exosomes (MDEs) and their uptake by different tumor and normal colon cells. Protein expression of <t>CD81</t> as a marker of exosomes and HSP70 as a negative control in MDEs ( a ). MDEs were analyzed by transmission electron microscopy using negative staining ( b ). Particle size distribution (by intensity) of isolated MDEs determined by DLS ( c ). Labeled milk exosomes isolated from human milk were incubated for 4 h with normal intestinal (CCD 841) or colon cancer (LS123) cells. Images were obtained by fluorescence microscope analysis ( d, e ). MiRNA-148a expression in CCD 841 and LS123 cells incubated with (EXO) or without (CONT) MDEs was analyzed by qRT-PCR ( f, g ). qRT-PCR results were calculated using the 2^(− ∆∆CT) method, and values were normalized against RNU6, *p < 0.05 t test
Anti Phospho Erk1 2, 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
https://www.bioz.com/product/cosmx+1000+plex+mrna+panel/ERK+1%2F2+Antibody/pm18772233-116-38-67
Average 96 stars, based on 1 article reviews
anti phospho erk1 2 - by Bioz Stars, 2026-10
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90
Cosmo Bio USA 1:1000 dilution of the primary antibody raised against chicken npy-y4 receptor antigen
Isolation of milk-derived exosomes (MDEs) and their uptake by different tumor and normal colon cells. Protein expression of <t>CD81</t> as a marker of exosomes and HSP70 as a negative control in MDEs ( a ). MDEs were analyzed by transmission electron microscopy using negative staining ( b ). Particle size distribution (by intensity) of isolated MDEs determined by DLS ( c ). Labeled milk exosomes isolated from human milk were incubated for 4 h with normal intestinal (CCD 841) or colon cancer (LS123) cells. Images were obtained by fluorescence microscope analysis ( d, e ). MiRNA-148a expression in CCD 841 and LS123 cells incubated with (EXO) or without (CONT) MDEs was analyzed by qRT-PCR ( f, g ). qRT-PCR results were calculated using the 2^(− ∆∆CT) method, and values were normalized against RNU6, *p < 0.05 t test
1:1000 Dilution Of The Primary Antibody Raised Against Chicken Npy Y4 Receptor Antigen, supplied by Cosmo Bio USA, 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/cosmx+1000+plex+mrna+panel/chicken+npy+y4+receptor+antibody/pm39121580-58-66-96
Average 90 stars, based on 1 article reviews
1:1000 dilution of the primary antibody raised against chicken npy-y4 receptor antigen - by Bioz Stars, 2026-10
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90
Cosmo Bio USA rabbit anti- octopus rhodopsin
Isolation of milk-derived exosomes (MDEs) and their uptake by different tumor and normal colon cells. Protein expression of <t>CD81</t> as a marker of exosomes and HSP70 as a negative control in MDEs ( a ). MDEs were analyzed by transmission electron microscopy using negative staining ( b ). Particle size distribution (by intensity) of isolated MDEs determined by DLS ( c ). Labeled milk exosomes isolated from human milk were incubated for 4 h with normal intestinal (CCD 841) or colon cancer (LS123) cells. Images were obtained by fluorescence microscope analysis ( d, e ). MiRNA-148a expression in CCD 841 and LS123 cells incubated with (EXO) or without (CONT) MDEs was analyzed by qRT-PCR ( f, g ). qRT-PCR results were calculated using the 2^(− ∆∆CT) method, and values were normalized against RNU6, *p < 0.05 t test
Rabbit Anti Octopus Rhodopsin, supplied by Cosmo Bio USA, 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/cosmx+1000+plex+mrna+panel/rabbit+anti+rhodopsin+antibody/pmc11556747-84-22-29
Average 90 stars, based on 1 article reviews
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Cosmo Bio USA rabbit 4r–tau cac–tip–4rt–p01 antibody
Isolation of milk-derived exosomes (MDEs) and their uptake by different tumor and normal colon cells. Protein expression of <t>CD81</t> as a marker of exosomes and HSP70 as a negative control in MDEs ( a ). MDEs were analyzed by transmission electron microscopy using negative staining ( b ). Particle size distribution (by intensity) of isolated MDEs determined by DLS ( c ). Labeled milk exosomes isolated from human milk were incubated for 4 h with normal intestinal (CCD 841) or colon cancer (LS123) cells. Images were obtained by fluorescence microscope analysis ( d, e ). MiRNA-148a expression in CCD 841 and LS123 cells incubated with (EXO) or without (CONT) MDEs was analyzed by qRT-PCR ( f, g ). qRT-PCR results were calculated using the 2^(− ∆∆CT) method, and values were normalized against RNU6, *p < 0.05 t test
Rabbit 4r–Tau Cac–Tip–4rt–P01 Antibody, supplied by Cosmo Bio USA, 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/cosmx+1000+plex+mrna+panel/anti+4rtau/pmc12138277-45-26-29
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rabbit 4r–tau cac–tip–4rt–p01 antibody - by Bioz Stars, 2026-10
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90
Cosmo Bio USA anti-homer2a/b
Isolation of milk-derived exosomes (MDEs) and their uptake by different tumor and normal colon cells. Protein expression of <t>CD81</t> as a marker of exosomes and HSP70 as a negative control in MDEs ( a ). MDEs were analyzed by transmission electron microscopy using negative staining ( b ). Particle size distribution (by intensity) of isolated MDEs determined by DLS ( c ). Labeled milk exosomes isolated from human milk were incubated for 4 h with normal intestinal (CCD 841) or colon cancer (LS123) cells. Images were obtained by fluorescence microscope analysis ( d, e ). MiRNA-148a expression in CCD 841 and LS123 cells incubated with (EXO) or without (CONT) MDEs was analyzed by qRT-PCR ( f, g ). qRT-PCR results were calculated using the 2^(− ∆∆CT) method, and values were normalized against RNU6, *p < 0.05 t test
Anti Homer2a/B, supplied by Cosmo Bio USA, 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/cosmx+1000+plex+mrna+panel/anti+homer2a+b/pmc03704219-302-0-1
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Image Search Results


DEX inhibits the proliferation of BMSCs. (A) Cell viability of BMSCs measured by CCK8. BMSCs were treated with different concentrations of DEX. (B) Western blot assay was conducted for determining the expression of cell growth factor IGF1. (C) ELISA was conducted for the quantitative analysis of IGF1 expression changes over time. The concentration of DEX was set as 10 −7 mol/L. * p < .05, ** p < .01, *** p < .001

Journal: Pharmacology Research & Perspectives

Article Title: Dexamethasone promotes the endoplasmic reticulum stress response of bone marrow mesenchymal stem cells by activating the PERK‐Nrf2 signaling pathway

doi: 10.1002/prp2.791

Figure Lengend Snippet: DEX inhibits the proliferation of BMSCs. (A) Cell viability of BMSCs measured by CCK8. BMSCs were treated with different concentrations of DEX. (B) Western blot assay was conducted for determining the expression of cell growth factor IGF1. (C) ELISA was conducted for the quantitative analysis of IGF1 expression changes over time. The concentration of DEX was set as 10 −7 mol/L. * p < .05, ** p < .01, *** p < .001

Article Snippet: For the detection of protein expression, the following antibodies were used: PERK (CST, 3192, 1:1000), ATF6 (Cosmo Bio, AM‐73‐500‐B, 1:1000), TFAR19 (Abcam, ab83958, 1:1000), IGF1 (Cosmo Bio, KM2076, 1:1000), IRE1a (Abcam, ab146176, 1:1000), NRF2 (Abcam, ab62352, 1:1000), β‐catenin (CST 8480, 1:1000).

Techniques: Western Blot, Expressing, Enzyme-linked Immunosorbent Assay, Concentration Assay

DEX activates ERS of BMSCs by the PERK‐Nrf2 pathway. (A) Western blot assay was conducted for determining the expression of p‐PERK in whole‐cell lysate and p‐Nrf2 in both whole‐cell lysate and nucleus. (B) Western blot assay was conducted for determining the expression of TEAR19 and IGF1 in BMSCs after treatment with Thapsigargin, DEX, and/or ML385. (C) Cell proliferation assay was conducted for detecting the cell viability of BMSCs after treatment with Thapsigargin, DEX, and/or ML385. (D) Quantitative results of flow cytometry showing the apoptosis extent of BMSC after treatment with Thapsigargin, DEX, and/or ML385. The concentration of DEX was set as 10 −7 mol/L.* p < .05, ** p < .01, *** p < .001

Journal: Pharmacology Research & Perspectives

Article Title: Dexamethasone promotes the endoplasmic reticulum stress response of bone marrow mesenchymal stem cells by activating the PERK‐Nrf2 signaling pathway

doi: 10.1002/prp2.791

Figure Lengend Snippet: DEX activates ERS of BMSCs by the PERK‐Nrf2 pathway. (A) Western blot assay was conducted for determining the expression of p‐PERK in whole‐cell lysate and p‐Nrf2 in both whole‐cell lysate and nucleus. (B) Western blot assay was conducted for determining the expression of TEAR19 and IGF1 in BMSCs after treatment with Thapsigargin, DEX, and/or ML385. (C) Cell proliferation assay was conducted for detecting the cell viability of BMSCs after treatment with Thapsigargin, DEX, and/or ML385. (D) Quantitative results of flow cytometry showing the apoptosis extent of BMSC after treatment with Thapsigargin, DEX, and/or ML385. The concentration of DEX was set as 10 −7 mol/L.* p < .05, ** p < .01, *** p < .001

Article Snippet: For the detection of protein expression, the following antibodies were used: PERK (CST, 3192, 1:1000), ATF6 (Cosmo Bio, AM‐73‐500‐B, 1:1000), TFAR19 (Abcam, ab83958, 1:1000), IGF1 (Cosmo Bio, KM2076, 1:1000), IRE1a (Abcam, ab146176, 1:1000), NRF2 (Abcam, ab62352, 1:1000), β‐catenin (CST 8480, 1:1000).

Techniques: Western Blot, Expressing, Proliferation Assay, Flow Cytometry, Concentration Assay

Isolation of milk-derived exosomes (MDEs) and their uptake by different tumor and normal colon cells. Protein expression of CD81 as a marker of exosomes and HSP70 as a negative control in MDEs ( a ). MDEs were analyzed by transmission electron microscopy using negative staining ( b ). Particle size distribution (by intensity) of isolated MDEs determined by DLS ( c ). Labeled milk exosomes isolated from human milk were incubated for 4 h with normal intestinal (CCD 841) or colon cancer (LS123) cells. Images were obtained by fluorescence microscope analysis ( d, e ). MiRNA-148a expression in CCD 841 and LS123 cells incubated with (EXO) or without (CONT) MDEs was analyzed by qRT-PCR ( f, g ). qRT-PCR results were calculated using the 2^(− ∆∆CT) method, and values were normalized against RNU6, *p < 0.05 t test

Journal: Journal of Translational Medicine

Article Title: Milk-derived exosomes (MDEs) have a different biological effect on normal fetal colon epithelial cells compared to colon tumor cells in a miRNA-dependent manner

doi: 10.1186/s12967-019-2072-3

Figure Lengend Snippet: Isolation of milk-derived exosomes (MDEs) and their uptake by different tumor and normal colon cells. Protein expression of CD81 as a marker of exosomes and HSP70 as a negative control in MDEs ( a ). MDEs were analyzed by transmission electron microscopy using negative staining ( b ). Particle size distribution (by intensity) of isolated MDEs determined by DLS ( c ). Labeled milk exosomes isolated from human milk were incubated for 4 h with normal intestinal (CCD 841) or colon cancer (LS123) cells. Images were obtained by fluorescence microscope analysis ( d, e ). MiRNA-148a expression in CCD 841 and LS123 cells incubated with (EXO) or without (CONT) MDEs was analyzed by qRT-PCR ( f, g ). qRT-PCR results were calculated using the 2^(− ∆∆CT) method, and values were normalized against RNU6, *p < 0.05 t test

Article Snippet: Primary antibodies were as follows: anti-β-catenin (1:2000; Sigma Aldrich, St Louis, MO, USA), anti-β-actin (1:1500; R&D Systems, Minneapolis, MN, USA), anti-collagen Iα1 (Affinity Bioreagents, Golden, CO, USA), anti-DNMT1 (1:1000; Cell Signaling Technology, Danvers, MA, USA), anti-PTEN (1:1000; Epitomics, Burlingame, CA, USA), anti HSP70 (1:1000; SBI System Biosciences, Palo Alto, CA, USA), and anti CD81 (1:1000; Cosmo Bio, Tokyo, Japan).

Techniques: Isolation, Derivative Assay, Expressing, Marker, Negative Control, Transmission Assay, Electron Microscopy, Negative Staining, Labeling, Incubation, Fluorescence, Microscopy, Quantitative RT-PCR