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human endoglin  (R&D Systems)


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    Structured Review

    R&D Systems human endoglin
    Human Endoglin, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/soluble+endoglin/Human+Soluble+Endoglin+ELISA+Kit+(Colorimetric)/pm38001975-57-20-22
    Average 93 stars, based on 6 article reviews
    human endoglin - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Clinical Proteomics:

    Article Title: Soluble endoglin reduces thrombus formation and platelet aggregation via interaction with αIIbβ3 integrin.
    Article Snippet: .. The levels of human sEng in plasma were measured using a specific kit for human soluble endoglin (R&D Systems). ..

    Article Title: Phenotypes of Pregnant Women Who Subsequently Develop Hypertension in Pregnancy
    Article Snippet: .. Plasma samples were stored at 80°C and were later quantified using ELISAs for placental growth factor (PlGF), soluble fms-like tyrosine kinase-1 (sFlt-1), soluble endoglin, myeloperoxidase and endothelin (R&D Systems, Burlington, Ontario, Canada), according to manufacturers’ instructions. ..

    Article Title: Phenotypes of Pregnant Women Who Subsequently Develop Hypertension in Pregnancy
    Article Snippet: .. Plasma samples were stored at −80°C and were later quantified using ELISAs for placental growth factor (PlGF), soluble fms‐like tyrosine kinase‐1 (sFlt‐1), soluble endoglin, myeloperoxidase and endothelin (R&D Systems, Burlington, Ontario, Canada), according to manufacturers' instructions. ..

    Enzyme-linked Immunosorbent Assay:

    Article Title: Preeclampsia at delivery is associated with lower serum vitamin D and higher antiangiogenic factors: a case control study
    Article Snippet: .. Soluble endoglin, and soluble flt-1 (also known as soluble vascular endothelial receptor 1 or s-VEGF-R1) were measured using manual enzyme linked immunosorbent assays (ELISA) from R&D Systems (Minneapolis, MN). ..

    Article Title: Vascular Biomarkers and Digital Ulcerations in Systemic Sclerosis: Results from a Randomized Controlled Trial of Oral Treprostinil (DISTOL-1)
    Article Snippet: Biomarker assays The following 16 markers of vascular injury and angiogenesis were measured in duplicate and quantified based on standard curve run at the same time as analysis using the MesoScale Discovery (MSD) platform (Meso Scale Diagnostics, Rockville, MD, USA): (1) Markers involved in angiogenesis – basic fibroblast growth factor (bFGF), placental growth factor (PIGF), soluble fms-like tyrosine kinase-1 (sFlt-1 or sVEGFR-1), an endothelium-specific receptor tyrosine kinase (Tie2 or Tek), vascular endothelial growth factors (VEGF, VEGF-C, VEGF-D) and hepatocyte growth factor (HGF); (2) Markers involved in inflammation - serum amyloid A (SAA) and C-reactive protein (CRP), and (3) Vascular markers - secreted intercellular adhesion molecule (ICAM-3), Endothelium leukocyte adhesion molecule (E-selectin), Platelet endothelial cell adhesion molecule (P-selectin), thrombomodulin, secreted intercellular adhesion molecule (ICAM-1), secreted vascular cell adhesion molecule (VCAM-1). .. Soluble endoglin and endostatin were also assayed in duplicate and quantified based on a standard curve by ELISA (R&D Systems, Inc., Minneapolis, MN, USA). ..



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    Circulating vascular injury and angiogenesis biomarkers after coronavirus disease 2019 (COVID‐19) infection. Plasma samples from healthy controls (0; n = 29), patients whose maximal respiratory support was supplemental oxygen (4, 5, 6; n = 49), and patients who required assisted ventilation (7, 8, 9; n = 22) were assessed for the following analytes using MesoScale Discovery multiplex immunoassays. (a) Serum amyloid A (SAA); (b) C‐reactive protein (CRP); (c) intercellular adhesion molecule 1 (ICAM‐1); (d) vascular cell adhesion molecule 1 (VCAM‐1); (e) E‐selectin; (f) thrombomodulin; (g) vascular endothelial growth factor A (VEGF‐A); (h) VEGFR1/Flt‐1; (i) placental growth factor (PlGF); (j) fibroblast growth factor (basic) (FGF(b)); (k) Tie‐2; (l) soluble <t>endoglin</t> (sENG) enzyme‐linked immunosorbent assay (ELISA); (m) bone morphogenetic protein 9 (BMP9) ELISA; (n) prodomain BMP10 (pBMP10) ELISA; (o) Pearson's correlation of circulating BMP9 and pBMP10 levels. p = 0.7415; (p) number of days patients were administered dexamethasone treatment before sample receipt; (q) Pearson's correlation of circulating BMP9 levels and dexamethasone treatment length. p = 0.3052; (r) circulating BMP9 levels of patient groups separated upon the time taken to be enrolled into the study. Sample receipt ≤7 days versus >7 days. All data presented as median–interquartile range. Kruskal–Wallis test. Dunn's multiple comparison test. ns, not significant; WHO, World Health Organization. p Values = *0.05; **0.01; ***0.001; ****0.0001.
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    Circulating vascular injury and angiogenesis biomarkers after coronavirus disease 2019 (COVID‐19) infection. Plasma samples from healthy controls (0; n = 29), patients whose maximal respiratory support was supplemental oxygen (4, 5, 6; n = 49), and patients who required assisted ventilation (7, 8, 9; n = 22) were assessed for the following analytes using MesoScale Discovery multiplex immunoassays. (a) Serum amyloid A (SAA); (b) C‐reactive protein (CRP); (c) intercellular adhesion molecule 1 (ICAM‐1); (d) vascular cell adhesion molecule 1 (VCAM‐1); (e) E‐selectin; (f) thrombomodulin; (g) vascular endothelial growth factor A (VEGF‐A); (h) VEGFR1/Flt‐1; (i) placental growth factor (PlGF); (j) fibroblast growth factor (basic) (FGF(b)); (k) Tie‐2; (l) soluble <t>endoglin</t> (sENG) enzyme‐linked immunosorbent assay (ELISA); (m) bone morphogenetic protein 9 (BMP9) ELISA; (n) prodomain BMP10 (pBMP10) ELISA; (o) Pearson's correlation of circulating BMP9 and pBMP10 levels. p = 0.7415; (p) number of days patients were administered dexamethasone treatment before sample receipt; (q) Pearson's correlation of circulating BMP9 levels and dexamethasone treatment length. p = 0.3052; (r) circulating BMP9 levels of patient groups separated upon the time taken to be enrolled into the study. Sample receipt ≤7 days versus >7 days. All data presented as median–interquartile range. Kruskal–Wallis test. Dunn's multiple comparison test. ns, not significant; WHO, World Health Organization. p Values = *0.05; **0.01; ***0.001; ****0.0001.
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    Antibodies for Western blot.

    Journal: Journal of Clinical Medicine

    Article Title: Molecular and Functional Cargo of Plasma-Derived Exosomes in Patients with Hereditary Hemorrhagic Telangiectasia

    doi: 10.3390/jcm13185430

    Figure Lengend Snippet: Antibodies for Western blot.

    Article Snippet: Soluble Endoglin , Santa Cruz (Santa Cruz, CA, USA), SC-20072 , 1:200 in 5% BSA , Mouse , 61 kDa , Reducing , PVDF.

    Techniques: Western Blot, Membrane

    Soluble Endoglin levels in HD and HHT exosomes. ( A ) Representative Western blot of HD and HHT exosomes for the angiogenesis-related protein sENG and the exosomal marker TSG101. Numbers below lanes indicate band intensities of sENG normalized to TSG101 using lane normalization factors. ( B ) Normalized sENG values of HD and HHT exosomes (n = 17). Age- and gender-matched pairs of HDs and HHT patients whose plasma was used for exosome isolation are connected by a line. ( C ) Normalized sENG values of HHT exosomes (n = 17) were correlated to total exosomal protein levels, as determined by Bicinchoninic acid (BCA) assay. Spearman’s rank correlation coefficient (r) and correlation significance (p) were calculated. ( D ) Normalized sENG values of HD exosomes (n = 17) were correlated to the total exosomal protein levels, as determined by BCA assay. Pearson coefficient of correlation (R2) and correlation significance (p) are shown.

    Journal: Journal of Clinical Medicine

    Article Title: Molecular and Functional Cargo of Plasma-Derived Exosomes in Patients with Hereditary Hemorrhagic Telangiectasia

    doi: 10.3390/jcm13185430

    Figure Lengend Snippet: Soluble Endoglin levels in HD and HHT exosomes. ( A ) Representative Western blot of HD and HHT exosomes for the angiogenesis-related protein sENG and the exosomal marker TSG101. Numbers below lanes indicate band intensities of sENG normalized to TSG101 using lane normalization factors. ( B ) Normalized sENG values of HD and HHT exosomes (n = 17). Age- and gender-matched pairs of HDs and HHT patients whose plasma was used for exosome isolation are connected by a line. ( C ) Normalized sENG values of HHT exosomes (n = 17) were correlated to total exosomal protein levels, as determined by Bicinchoninic acid (BCA) assay. Spearman’s rank correlation coefficient (r) and correlation significance (p) were calculated. ( D ) Normalized sENG values of HD exosomes (n = 17) were correlated to the total exosomal protein levels, as determined by BCA assay. Pearson coefficient of correlation (R2) and correlation significance (p) are shown.

    Article Snippet: Soluble Endoglin , Santa Cruz (Santa Cruz, CA, USA), SC-20072 , 1:200 in 5% BSA , Mouse , 61 kDa , Reducing , PVDF.

    Techniques: Western Blot, Marker, Clinical Proteomics, Isolation, BIA-KA

    Circulating vascular injury and angiogenesis biomarkers after coronavirus disease 2019 (COVID‐19) infection. Plasma samples from healthy controls (0; n = 29), patients whose maximal respiratory support was supplemental oxygen (4, 5, 6; n = 49), and patients who required assisted ventilation (7, 8, 9; n = 22) were assessed for the following analytes using MesoScale Discovery multiplex immunoassays. (a) Serum amyloid A (SAA); (b) C‐reactive protein (CRP); (c) intercellular adhesion molecule 1 (ICAM‐1); (d) vascular cell adhesion molecule 1 (VCAM‐1); (e) E‐selectin; (f) thrombomodulin; (g) vascular endothelial growth factor A (VEGF‐A); (h) VEGFR1/Flt‐1; (i) placental growth factor (PlGF); (j) fibroblast growth factor (basic) (FGF(b)); (k) Tie‐2; (l) soluble endoglin (sENG) enzyme‐linked immunosorbent assay (ELISA); (m) bone morphogenetic protein 9 (BMP9) ELISA; (n) prodomain BMP10 (pBMP10) ELISA; (o) Pearson's correlation of circulating BMP9 and pBMP10 levels. p = 0.7415; (p) number of days patients were administered dexamethasone treatment before sample receipt; (q) Pearson's correlation of circulating BMP9 levels and dexamethasone treatment length. p = 0.3052; (r) circulating BMP9 levels of patient groups separated upon the time taken to be enrolled into the study. Sample receipt ≤7 days versus >7 days. All data presented as median–interquartile range. Kruskal–Wallis test. Dunn's multiple comparison test. ns, not significant; WHO, World Health Organization. p Values = *0.05; **0.01; ***0.001; ****0.0001.

    Journal: Pulmonary Circulation

    Article Title: Reduced circulating BMP9 and pBMP10 in hospitalized COVID‐19 patients

    doi: 10.1002/pul2.12192

    Figure Lengend Snippet: Circulating vascular injury and angiogenesis biomarkers after coronavirus disease 2019 (COVID‐19) infection. Plasma samples from healthy controls (0; n = 29), patients whose maximal respiratory support was supplemental oxygen (4, 5, 6; n = 49), and patients who required assisted ventilation (7, 8, 9; n = 22) were assessed for the following analytes using MesoScale Discovery multiplex immunoassays. (a) Serum amyloid A (SAA); (b) C‐reactive protein (CRP); (c) intercellular adhesion molecule 1 (ICAM‐1); (d) vascular cell adhesion molecule 1 (VCAM‐1); (e) E‐selectin; (f) thrombomodulin; (g) vascular endothelial growth factor A (VEGF‐A); (h) VEGFR1/Flt‐1; (i) placental growth factor (PlGF); (j) fibroblast growth factor (basic) (FGF(b)); (k) Tie‐2; (l) soluble endoglin (sENG) enzyme‐linked immunosorbent assay (ELISA); (m) bone morphogenetic protein 9 (BMP9) ELISA; (n) prodomain BMP10 (pBMP10) ELISA; (o) Pearson's correlation of circulating BMP9 and pBMP10 levels. p = 0.7415; (p) number of days patients were administered dexamethasone treatment before sample receipt; (q) Pearson's correlation of circulating BMP9 levels and dexamethasone treatment length. p = 0.3052; (r) circulating BMP9 levels of patient groups separated upon the time taken to be enrolled into the study. Sample receipt ≤7 days versus >7 days. All data presented as median–interquartile range. Kruskal–Wallis test. Dunn's multiple comparison test. ns, not significant; WHO, World Health Organization. p Values = *0.05; **0.01; ***0.001; ****0.0001.

    Article Snippet: Enzyme‐linked immunosorbent assays (ELISAs) for BMP9 and pBMP10 were conducted as previously described., The soluble endoglin Quantikine assay (R&D Systems) was performed according to the manufacturer's instructions.

    Techniques: Infection, Multiplex Assay, Enzyme-linked Immunosorbent Assay, Comparison