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You searched for: EV210382 (EV-TRACK ID)

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Experiment number
  • If needed, multiple experiments were identified in a single publication based on differing sample types, separation protocols and/or vesicle types of interest.
Species
  • Species of origin of the EVs.
Separation protocol
  • Gives a short, non-chronological overview of the different steps of the separation protocol.
    • (d)(U)C = (differential) (ultra)centrifugation
    • DG = density gradient
    • UF = ultrafiltration
    • SEC = size-exclusion chromatography
    • IAF = immuno-affinity capture
Details EV-TRACK ID Experiment nr. Species Sample type Separation protocol First author Year EV-METRIC
EV210382 1/4 Homo sapiens maternal placenta perfusate (d)(U)C Awoyemi T 2023 78%

Study summary

Full title
All authors
Awoyemi T, Zhang W, Rahbar M, Cribbs A, Logenthiran P, Jiang S, Collett G, Cerdeira AS, Vatish M
Journal
Front Cardiovasc Med
Abstract
Preeclampsia (PE) is a pregnancy-specific hypertensive disorder affecting 2%-8% of pregnancies world (show more...)Preeclampsia (PE) is a pregnancy-specific hypertensive disorder affecting 2%-8% of pregnancies worldwide. Biomarker(s) for the disorder exists, but while these have excellent negative predictive value, their positive predictive value is poor. Extracellular vesicles released by the placenta into the maternal circulation, syncytiotrophoblast membrane extracellular vesicles (STB-EVs), have been identified as being involved in PE with the potential to act as liquid biopsies. (hide)
EV-METRIC
78% (50th percentile of all experiments on the same sample type)
 Reported
 Not reported
 Not applicable
EV-enriched proteins
Protein analysis: analysis of three or more EV-enriched proteins
non EV-enriched protein
Protein analysis: assessment of a non-EV-enriched protein
qualitative and quantitative analysis
Particle analysis: implementation of both qualitative and quantitative methods. For the quantitative method, the reporting of measured EV concentration is expected.
electron microscopy images
Particle analysis: inclusion of a widefield and close-up electron microscopy image
density gradient
Separation method: density gradient, at least as validation of results attributed to EVs
EV density
Separation method: reporting of obtained EV density
ultracentrifugation specifics
Separation method: reporting of g-forces, duration and rotor type of ultracentrifugation steps
antibody specifics
Protein analysis: antibody clone/reference number and dilution
lysate preparation
Protein analysis: lysis buffer composition
Study data
Sample type
maternal placenta perfusate
Sample origin
Control condition
Focus vesicles
medium/large extracellular vesicle
Separation protocol
Separation protocol
  • Gives a short, non-chronological overview of the
    different steps of the separation protocol.
    • dUC = (Differential) (ultra)centrifugation
    • DG = density gradient
    • UF = ultrafiltration
    • SEC = size-exclusion chromatography
    • IAF = immuno-affinity capture
(Differential) (ultra)centrifugation
Protein markers
EV: Alix/ PLAP/ CD9
non-EV: Cytochrome C
Proteomics
yes
Show all info
Study aim
Biomarker/Identification of content (omics approaches)
Sample
Species
Homo sapiens
Sample Type
maternal placenta perfusate
Separation Method
(Differential) (ultra)centrifugation
dUC: centrifugation steps
Between 10,000 g and 50,000 g
Pelleting performed
Yes
Pelleting: time(min)
30
Pelleting: rotor type
Sorvall TST28.39
Pelleting: speed (g)
10,000
Wash: volume per pellet (ml)
45
Wash: time (min)
30
Wash: Rotor Type
Sorvall TST28.39
Wash: speed (g)
10,000
Characterization: Protein analysis
Protein Concentration Method
BCA
Protein Yield (µg)
8680-10240
Western Blot
Antibody details provided?
No
Detected EV-associated proteins
Alix/ PLAP
Not detected EV-associated proteins
CD9
Not detected contaminants
Cytochrome C
Proteomics database
PRIDE
Characterization: RNA analysis
RNA analysis
Type
(RT)-(q)PCR/ RNA-sequencing/ Capillary electrophoresis (e.g. Bioanalyzer)
Database
NCBI geo
Proteinase treatment
No
RNAse treatment
No
Characterization: Lipid analysis
No
Characterization: Particle analysis
NTA
Report type
Modus
Reported size (nm)
205.8
EV concentration
Yes
Particle yield
6.98E11-1.12E12
EM
EM-type
Transmission-EM
Image type
Close-up, Wide-field
EV210382 2/4 Homo sapiens maternal placenta perfusate (d)(U)C Awoyemi T 2023 78%

Study summary

Full title
All authors
Awoyemi T, Zhang W, Rahbar M, Cribbs A, Logenthiran P, Jiang S, Collett G, Cerdeira AS, Vatish M
Journal
Front Cardiovasc Med
Abstract
Preeclampsia (PE) is a pregnancy-specific hypertensive disorder affecting 2%-8% of pregnancies world (show more...)Preeclampsia (PE) is a pregnancy-specific hypertensive disorder affecting 2%-8% of pregnancies worldwide. Biomarker(s) for the disorder exists, but while these have excellent negative predictive value, their positive predictive value is poor. Extracellular vesicles released by the placenta into the maternal circulation, syncytiotrophoblast membrane extracellular vesicles (STB-EVs), have been identified as being involved in PE with the potential to act as liquid biopsies. (hide)
EV-METRIC
78% (50th percentile of all experiments on the same sample type)
 Reported
 Not reported
 Not applicable
EV-enriched proteins
Protein analysis: analysis of three or more EV-enriched proteins
non EV-enriched protein
Protein analysis: assessment of a non-EV-enriched protein
qualitative and quantitative analysis
Particle analysis: implementation of both qualitative and quantitative methods. For the quantitative method, the reporting of measured EV concentration is expected.
electron microscopy images
Particle analysis: inclusion of a widefield and close-up electron microscopy image
density gradient
Separation method: density gradient, at least as validation of results attributed to EVs
EV density
Separation method: reporting of obtained EV density
ultracentrifugation specifics
Separation method: reporting of g-forces, duration and rotor type of ultracentrifugation steps
antibody specifics
Protein analysis: antibody clone/reference number and dilution
lysate preparation
Protein analysis: lysis buffer composition
Study data
Sample type
maternal placenta perfusate
Sample origin
Control condition
Focus vesicles
small extracellular vesicle
Separation protocol
Separation protocol
  • Gives a short, non-chronological overview of the
    different steps of the separation protocol.
    • dUC = (Differential) (ultra)centrifugation
    • DG = density gradient
    • UF = ultrafiltration
    • SEC = size-exclusion chromatography
    • IAF = immuno-affinity capture
(Differential) (ultra)centrifugation
Protein markers
EV: Alix/ CD63/ PLAP/ CD9
non-EV: Cytochrome C
Proteomics
yes
Show all info
Study aim
Biomarker/Identification of content (omics approaches)
Sample
Species
Homo sapiens
Sample Type
maternal placenta perfusate
Separation Method
(Differential) (ultra)centrifugation
dUC: centrifugation steps
Between 10,000 g and 50,000 g
Equal to or above 150,000 g
Pelleting performed
Yes
Pelleting: time(min)
120
Pelleting: rotor type
Sorvall TST28.39
Pelleting: speed (g)
150,000
Wash: volume per pellet (ml)
45
Wash: time (min)
120
Wash: Rotor Type
Sorvall TST28.39
Wash: speed (g)
150,000
Characterization: Protein analysis
Protein Concentration Method
BCA
Protein Yield (µg)
2250-3040
Western Blot
Antibody details provided?
No
Detected EV-associated proteins
Alix/ CD63/ PLAP
Not detected EV-associated proteins
CD9
Not detected contaminants
Cytochrome C
Flow cytometry
Type of Flow cytometry
A BD LSRII flow cytometer (BD Biosciences) with a blue, violet, and red laser
Calibration bead size
0.11/ 0.18/ 0.24/ 0.30/ 0.50/ 0.59/ 0.88/ 1.30
Antibody details provided?
No
Proteomics database
PRIDE
Characterization: RNA analysis
RNA analysis
Type
(RT)-(q)PCR/ RNA-sequencing/ Capillary electrophoresis (e.g. Bioanalyzer)
Database
NCBI geo
Proteinase treatment
No
RNAse treatment
No
Characterization: Lipid analysis
No
Characterization: Particle analysis
NTA
Report type
Modus
Reported size (nm)
479
EV concentration
Yes
Particle yield
1.59E11-1.78E11
EM
EM-type
Transmission-EM
Image type
Close-up, Wide-field
EV210382 3/4 Homo sapiens maternal placenta perfusate (d)(U)C Awoyemi T 2023 78%

Study summary

Full title
All authors
Awoyemi T, Zhang W, Rahbar M, Cribbs A, Logenthiran P, Jiang S, Collett G, Cerdeira AS, Vatish M
Journal
Front Cardiovasc Med
Abstract
Preeclampsia (PE) is a pregnancy-specific hypertensive disorder affecting 2%-8% of pregnancies world (show more...)Preeclampsia (PE) is a pregnancy-specific hypertensive disorder affecting 2%-8% of pregnancies worldwide. Biomarker(s) for the disorder exists, but while these have excellent negative predictive value, their positive predictive value is poor. Extracellular vesicles released by the placenta into the maternal circulation, syncytiotrophoblast membrane extracellular vesicles (STB-EVs), have been identified as being involved in PE with the potential to act as liquid biopsies. (hide)
EV-METRIC
78% (50th percentile of all experiments on the same sample type)
 Reported
 Not reported
 Not applicable
EV-enriched proteins
Protein analysis: analysis of three or more EV-enriched proteins
non EV-enriched protein
Protein analysis: assessment of a non-EV-enriched protein
qualitative and quantitative analysis
Particle analysis: implementation of both qualitative and quantitative methods. For the quantitative method, the reporting of measured EV concentration is expected.
electron microscopy images
Particle analysis: inclusion of a widefield and close-up electron microscopy image
density gradient
Separation method: density gradient, at least as validation of results attributed to EVs
EV density
Separation method: reporting of obtained EV density
ultracentrifugation specifics
Separation method: reporting of g-forces, duration and rotor type of ultracentrifugation steps
antibody specifics
Protein analysis: antibody clone/reference number and dilution
lysate preparation
Protein analysis: lysis buffer composition
Study data
Sample type
maternal placenta perfusate
Sample origin
Preeclampsia
Focus vesicles
medium/large extracellular vesicle
Separation protocol
Separation protocol
  • Gives a short, non-chronological overview of the
    different steps of the separation protocol.
    • dUC = (Differential) (ultra)centrifugation
    • DG = density gradient
    • UF = ultrafiltration
    • SEC = size-exclusion chromatography
    • IAF = immuno-affinity capture
(Differential) (ultra)centrifugation
Protein markers
EV: CD63/ PLAP/ CD9
non-EV: Cytochrome C
Proteomics
yes
Show all info
Study aim
Biomarker/Identification of content (omics approaches)
Sample
Species
Homo sapiens
Sample Type
maternal placenta perfusate
Separation Method
(Differential) (ultra)centrifugation
dUC: centrifugation steps
Between 10,000 g and 50,000 g
Pelleting performed
Yes
Pelleting: time(min)
30
Pelleting: rotor type
Sorvall TST28.39
Pelleting: speed (g)
10,000
Wash: volume per pellet (ml)
45
Wash: time (min)
30
Wash: Rotor Type
Sorvall TST28.39
Wash: speed (g)
10,000
Characterization: Protein analysis
Protein Concentration Method
BCA
Protein Yield (µg)
10460-21650
Western Blot
Antibody details provided?
No
Detected EV-associated proteins
CD63/ PLAP
Not detected EV-associated proteins
CD9
Not detected contaminants
Cytochrome C
Proteomics database
PRIDE
Characterization: RNA analysis
RNA analysis
Type
(RT)-(q)PCR/ RNA-sequencing/ Capillary electrophoresis (e.g. Bioanalyzer)
Database
NCBI geo
Proteinase treatment
No
RNAse treatment
No
Characterization: Lipid analysis
No
Characterization: Particle analysis
NTA
Report type
Modus
Reported size (nm)
205.8
EV concentration
Yes
Particle yield
3.75E11-1E12
EM
EM-type
Transmission-EM
Image type
Close-up, Wide-field
EV210382 4/4 Homo sapiens maternal placenta perfusate (d)(U)C Awoyemi T 2023 78%

Study summary

Full title
All authors
Awoyemi T, Zhang W, Rahbar M, Cribbs A, Logenthiran P, Jiang S, Collett G, Cerdeira AS, Vatish M
Journal
Front Cardiovasc Med
Abstract
Preeclampsia (PE) is a pregnancy-specific hypertensive disorder affecting 2%-8% of pregnancies world (show more...)Preeclampsia (PE) is a pregnancy-specific hypertensive disorder affecting 2%-8% of pregnancies worldwide. Biomarker(s) for the disorder exists, but while these have excellent negative predictive value, their positive predictive value is poor. Extracellular vesicles released by the placenta into the maternal circulation, syncytiotrophoblast membrane extracellular vesicles (STB-EVs), have been identified as being involved in PE with the potential to act as liquid biopsies. (hide)
EV-METRIC
78% (50th percentile of all experiments on the same sample type)
 Reported
 Not reported
 Not applicable
EV-enriched proteins
Protein analysis: analysis of three or more EV-enriched proteins
non EV-enriched protein
Protein analysis: assessment of a non-EV-enriched protein
qualitative and quantitative analysis
Particle analysis: implementation of both qualitative and quantitative methods. For the quantitative method, the reporting of measured EV concentration is expected.
electron microscopy images
Particle analysis: inclusion of a widefield and close-up electron microscopy image
density gradient
Separation method: density gradient, at least as validation of results attributed to EVs
EV density
Separation method: reporting of obtained EV density
ultracentrifugation specifics
Separation method: reporting of g-forces, duration and rotor type of ultracentrifugation steps
antibody specifics
Protein analysis: antibody clone/reference number and dilution
lysate preparation
Protein analysis: lysis buffer composition
Study data
Sample type
maternal placenta perfusate
Sample origin
Preeclampsia
Focus vesicles
small extracellular vesicle
Separation protocol
Separation protocol
  • Gives a short, non-chronological overview of the
    different steps of the separation protocol.
    • dUC = (Differential) (ultra)centrifugation
    • DG = density gradient
    • UF = ultrafiltration
    • SEC = size-exclusion chromatography
    • IAF = immuno-affinity capture
(Differential) (ultra)centrifugation
Protein markers
EV: Alix/ CD63/ PLAP/ CD9
non-EV: Cytochrome C
Proteomics
yes
Show all info
Study aim
Biomarker/Identification of content (omics approaches)
Sample
Species
Homo sapiens
Sample Type
maternal placenta perfusate
Separation Method
(Differential) (ultra)centrifugation
dUC: centrifugation steps
Between 10,000 g and 50,000 g
Equal to or above 150,000 g
Pelleting performed
Yes
Pelleting: time(min)
120
Pelleting: rotor type
Sorvall TST28.39
Pelleting: speed (g)
150,000
Wash: volume per pellet (ml)
45
Wash: time (min)
120
Wash: Rotor Type
Sorvall TST28.39
Wash: speed (g)
150,000
Characterization: Protein analysis
Protein Concentration Method
BCA
Protein Yield (µg)
5780-10648
Western Blot
Antibody details provided?
No
Detected EV-associated proteins
Alix/ CD63/ PLAP
Not detected EV-associated proteins
CD9
Not detected contaminants
Cytochrome C
Flow cytometry
Type of Flow cytometry
A BD LSRII flow cytometer (BD Biosciences) with a blue, violet, and red laser
Calibration bead size
0.11/ 0.18/ 0.24/ 0.30/ 0.50/ 0.59/ 0.88/ 1.30
Antibody details provided?
No
Proteomics database
PRIDE
Characterization: RNA analysis
RNA analysis
Type
(RT)-(q)PCR/ RNA-sequencing/ Capillary electrophoresis (e.g. Bioanalyzer)
Database
NCBI geo
Proteinase treatment
No
RNAse treatment
No
Characterization: Lipid analysis
No
Characterization: Particle analysis
NTA
Report type
Modus
Reported size (nm)
479
EV concentration
Yes
Particle yield
2.2E11-7.2E11
EM
EM-type
Transmission-EM
Image type
Close-up, Wide-field
1 - 4 of 4
  • CM = Commercial method
  • dUC = differential ultracentrifugation
  • DG = density gradient
  • UF = ultrafiltration
  • SEC = size-exclusion chromatography
EV-TRACK ID
EV210382
species
Homo sapiens
sample type
maternal
placenta perfusate
condition
Control condition
Control condition
Preeclampsia
Preeclampsia
separation protocol
dUC
dUC
dUC
dUC
vesicle related term
medium/large EV
small EV
medium/large EV
small EV
Exp. nr.
1
2
3
4
EV-METRIC %
78
78
78
78