cell death 6 Search Results


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Multifunctional protein involved in endocytosis, multivesicular body biogenesis, membrane repair, cytokinesis, apoptosis and maintenance of tight junction integrity. Class E VPS protein involved in concentration and sorting of cargo proteins of the multivesicular body (MVB)
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Cusabio alix
EV characteristics of mortality cohort. ( A ) EV morphology and size were visualized using electron microscopy (scale bar = 200 nm). ( B ) Plasma EVs from alive (n = 8) and individuals who had died (n = 8) within 5 years of sample collection were lysed and the EV <t>markers</t> <t>CD81</t> and <t>ALIX</t> using quantified using ELISA assays. Individual data points are shown, and the bar represents the mean. There were no significant differences in CD81 and ALIX EV levels between alive and deceased individuals using Student’s t-test. ( C ) EV markers in plasma EVs were assessed using an Exo-Check™ Exosome Antibody Array. ( D,E ) Plasma EVs were isolated from participants who were alive or died within five years of sample donation (Table ), and EV size distribution and concentration were analyzed by Nanoparticle Tracking Analysis. ( D ) Size distribution was averaged for each group (n = 75 for alive and n = 74 for died groups). EV concentration is shown in the plots in ( E ).
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Proteintech alg 2
EV characteristics of mortality cohort. ( A ) EV morphology and size were visualized using electron microscopy (scale bar = 200 nm). ( B ) Plasma EVs from alive (n = 8) and individuals who had died (n = 8) within 5 years of sample collection were lysed and the EV <t>markers</t> <t>CD81</t> and <t>ALIX</t> using quantified using ELISA assays. Individual data points are shown, and the bar represents the mean. There were no significant differences in CD81 and ALIX EV levels between alive and deceased individuals using Student’s t-test. ( C ) EV markers in plasma EVs were assessed using an Exo-Check™ Exosome Antibody Array. ( D,E ) Plasma EVs were isolated from participants who were alive or died within five years of sample donation (Table ), and EV size distribution and concentration were analyzed by Nanoparticle Tracking Analysis. ( D ) Size distribution was averaged for each group (n = 75 for alive and n = 74 for died groups). EV concentration is shown in the plots in ( E ).
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https://www.bioz.com/product/cell+death+6/PDCD6+Antibody/pmc10200693-20-0-6
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Bio X Cell monoclonal ab
EV characteristics of mortality cohort. ( A ) EV morphology and size were visualized using electron microscopy (scale bar = 200 nm). ( B ) Plasma EVs from alive (n = 8) and individuals who had died (n = 8) within 5 years of sample collection were lysed and the EV <t>markers</t> <t>CD81</t> and <t>ALIX</t> using quantified using ELISA assays. Individual data points are shown, and the bar represents the mean. There were no significant differences in CD81 and ALIX EV levels between alive and deceased individuals using Student’s t-test. ( C ) EV markers in plasma EVs were assessed using an Exo-Check™ Exosome Antibody Array. ( D,E ) Plasma EVs were isolated from participants who were alive or died within five years of sample donation (Table ), and EV size distribution and concentration were analyzed by Nanoparticle Tracking Analysis. ( D ) Size distribution was averaged for each group (n = 75 for alive and n = 74 for died groups). EV concentration is shown in the plots in ( E ).
Monoclonal Ab, supplied by Bio X Cell, 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/cell+death+6/Anti-ALIX%2FPDCD6IP+Antibody+Picoband/pm30677097-244-13-15
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Bio X Cell anti programmed cell death protein 1 pd 1
EV characteristics of mortality cohort. ( A ) EV morphology and size were visualized using electron microscopy (scale bar = 200 nm). ( B ) Plasma EVs from alive (n = 8) and individuals who had died (n = 8) within 5 years of sample collection were lysed and the EV <t>markers</t> <t>CD81</t> and <t>ALIX</t> using quantified using ELISA assays. Individual data points are shown, and the bar represents the mean. There were no significant differences in CD81 and ALIX EV levels between alive and deceased individuals using Student’s t-test. ( C ) EV markers in plasma EVs were assessed using an Exo-Check™ Exosome Antibody Array. ( D,E ) Plasma EVs were isolated from participants who were alive or died within five years of sample donation (Table ), and EV size distribution and concentration were analyzed by Nanoparticle Tracking Analysis. ( D ) Size distribution was averaged for each group (n = 75 for alive and n = 74 for died groups). EV concentration is shown in the plots in ( E ).
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Bio-Techne corporation alix antibody (3a9) - bsa free
EV characteristics of mortality cohort. ( A ) EV morphology and size were visualized using electron microscopy (scale bar = 200 nm). ( B ) Plasma EVs from alive (n = 8) and individuals who had died (n = 8) within 5 years of sample collection were lysed and the EV <t>markers</t> <t>CD81</t> and <t>ALIX</t> using quantified using ELISA assays. Individual data points are shown, and the bar represents the mean. There were no significant differences in CD81 and ALIX EV levels between alive and deceased individuals using Student’s t-test. ( C ) EV markers in plasma EVs were assessed using an Exo-Check™ Exosome Antibody Array. ( D,E ) Plasma EVs were isolated from participants who were alive or died within five years of sample donation (Table ), and EV size distribution and concentration were analyzed by Nanoparticle Tracking Analysis. ( D ) Size distribution was averaged for each group (n = 75 for alive and n = 74 for died groups). EV concentration is shown in the plots in ( E ).
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https://www.bioz.com/product/cell+death+6/Alix+Antibody+(3A9)+-+BSA+Free/bio-techne+corporation___nb100-65678
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Gallus BioPharmaceuticals programmed cell death 6-interacting protein
EV characteristics of mortality cohort. ( A ) EV morphology and size were visualized using electron microscopy (scale bar = 200 nm). ( B ) Plasma EVs from alive (n = 8) and individuals who had died (n = 8) within 5 years of sample collection were lysed and the EV <t>markers</t> <t>CD81</t> and <t>ALIX</t> using quantified using ELISA assays. Individual data points are shown, and the bar represents the mean. There were no significant differences in CD81 and ALIX EV levels between alive and deceased individuals using Student’s t-test. ( C ) EV markers in plasma EVs were assessed using an Exo-Check™ Exosome Antibody Array. ( D,E ) Plasma EVs were isolated from participants who were alive or died within five years of sample donation (Table ), and EV size distribution and concentration were analyzed by Nanoparticle Tracking Analysis. ( D ) Size distribution was averaged for each group (n = 75 for alive and n = 74 for died groups). EV concentration is shown in the plots in ( E ).
Programmed Cell Death 6 Interacting Protein, supplied by Gallus BioPharmaceuticals, 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/cell+death+6/programmed+cell+death+6+interacting+protein/pm25452148-205-12-21
Average 90 stars, based on 1 article reviews
programmed cell death 6-interacting protein - by Bioz Stars, 2026-10
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N/A
PDCD6 produced in E.Coli is a single, non-glycosylated olypeptide chain containing 211 amino acids (1-191a.a.) and having a molecular mass of 24.0 kDa. PDCD6 is fused to a 20 amino acid His-tag at N-terminus &
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N/A
Programmed Cell Death 6 Antibody is a Rabbit Polyclonal antibody against Programmed Cell Death 6
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N/A
Programmed Cell Death 6 Interacting Protein Antibody is a Rabbit Polyclonal antibody against Programmed Cell Death 6 Interacting Protein
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N/A
Programmed Cell Death 6, Human Recombinant; 10 ug
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Image Search Results


EV characteristics of mortality cohort. ( A ) EV morphology and size were visualized using electron microscopy (scale bar = 200 nm). ( B ) Plasma EVs from alive (n = 8) and individuals who had died (n = 8) within 5 years of sample collection were lysed and the EV markers CD81 and ALIX using quantified using ELISA assays. Individual data points are shown, and the bar represents the mean. There were no significant differences in CD81 and ALIX EV levels between alive and deceased individuals using Student’s t-test. ( C ) EV markers in plasma EVs were assessed using an Exo-Check™ Exosome Antibody Array. ( D,E ) Plasma EVs were isolated from participants who were alive or died within five years of sample donation (Table ), and EV size distribution and concentration were analyzed by Nanoparticle Tracking Analysis. ( D ) Size distribution was averaged for each group (n = 75 for alive and n = 74 for died groups). EV concentration is shown in the plots in ( E ).

Journal: Scientific Reports

Article Title: Association of extracellular vesicle inflammatory proteins and mortality

doi: 10.1038/s41598-022-17944-z

Figure Lengend Snippet: EV characteristics of mortality cohort. ( A ) EV morphology and size were visualized using electron microscopy (scale bar = 200 nm). ( B ) Plasma EVs from alive (n = 8) and individuals who had died (n = 8) within 5 years of sample collection were lysed and the EV markers CD81 and ALIX using quantified using ELISA assays. Individual data points are shown, and the bar represents the mean. There were no significant differences in CD81 and ALIX EV levels between alive and deceased individuals using Student’s t-test. ( C ) EV markers in plasma EVs were assessed using an Exo-Check™ Exosome Antibody Array. ( D,E ) Plasma EVs were isolated from participants who were alive or died within five years of sample donation (Table ), and EV size distribution and concentration were analyzed by Nanoparticle Tracking Analysis. ( D ) Size distribution was averaged for each group (n = 75 for alive and n = 74 for died groups). EV concentration is shown in the plots in ( E ).

Article Snippet: Equal concentrations of EV lysates were used to quantitatively measure the EV markers CD81 (CSB-EL004960HU) and ALIX (CSB-EL017673HU) using kits from CUSABIO according to manufacturer’s instructions.

Techniques: Electron Microscopy, Clinical Proteomics, Enzyme-linked Immunosorbent Assay, Ab Array, Isolation, Concentration Assay