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rat platelet derived growth factor pdgf  (Elabscience Biotechnology)


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    Structured Review

    Elabscience Biotechnology rat platelet derived growth factor pdgf
    Rat Platelet Derived Growth Factor Pdgf, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/platelet+derived+growth+factor+bb/Rat+PDGF-BB+(Platelet+Derived+Growth+Factor+BB)+ELISA+Kit/pm41922477-62-16-14
    Average 94 stars, based on 11 article reviews
    rat platelet derived growth factor pdgf - by Bioz Stars, 2026-09
    94/100 stars

    Images

    Related Articles

    Derivative Assay:

    Article Title: Autologous Blood Clot Therapy for Wounds: Investigating the Chemotactic Effect on PBMCs and Fibroblasts in Diabetes.
    Article Snippet: Protein concentration within the clot secretome was determined spectrophotometrically using the Direct UV method (Nano- drop, Jenway; 7415, Cole- Parmer, USA). .. The concentrations of platelet- derived growth factor- BB (PDGF- BB) (E- EL- H1577, Elabscience, USA), P- selectin (SEA569Hu; Cloud- Clone Corp, USA) and CCL- 5 (Proteintech, USA) were determined using sandwich ELISA assays and the absorbance read at 450 nm using a microplate reader (Multiskan Note: Control participants had either < 2 metabolic risk factors or ≤ 1 indicator of obesity/visceral adiposity with no other metabolic risk factors. ..

    Sandwich ELISA:

    Article Title: Autologous Blood Clot Therapy for Wounds: Investigating the Chemotactic Effect on PBMCs and Fibroblasts in Diabetes.
    Article Snippet: Protein concentration within the clot secretome was determined spectrophotometrically using the Direct UV method (Nano- drop, Jenway; 7415, Cole- Parmer, USA). .. The concentrations of platelet- derived growth factor- BB (PDGF- BB) (E- EL- H1577, Elabscience, USA), P- selectin (SEA569Hu; Cloud- Clone Corp, USA) and CCL- 5 (Proteintech, USA) were determined using sandwich ELISA assays and the absorbance read at 450 nm using a microplate reader (Multiskan Note: Control participants had either < 2 metabolic risk factors or ≤ 1 indicator of obesity/visceral adiposity with no other metabolic risk factors. ..

    Control:

    Article Title: Autologous Blood Clot Therapy for Wounds: Investigating the Chemotactic Effect on PBMCs and Fibroblasts in Diabetes.
    Article Snippet: Protein concentration within the clot secretome was determined spectrophotometrically using the Direct UV method (Nano- drop, Jenway; 7415, Cole- Parmer, USA). .. The concentrations of platelet- derived growth factor- BB (PDGF- BB) (E- EL- H1577, Elabscience, USA), P- selectin (SEA569Hu; Cloud- Clone Corp, USA) and CCL- 5 (Proteintech, USA) were determined using sandwich ELISA assays and the absorbance read at 450 nm using a microplate reader (Multiskan Note: Control participants had either < 2 metabolic risk factors or ≤ 1 indicator of obesity/visceral adiposity with no other metabolic risk factors. ..

    Multiple Displacement Amplification:

    Article Title: Wound healing potential of palm oil tocotrienols rich fraction
    Article Snippet: .. The serum was used for plasmaderived growth factor-BB, Platelet-derived growth factor -BB (E-EL-R0537-Elabscience) and Malondialdehyde, MDA (E-EL-0060-Elabscience) content testing using Elisa kit– based on manufacturer’s procedure (Elabscience, Texas, USA). eISSN: 2550-2166 © 2021 The Authors. ..

    Enzyme-linked Immunosorbent Assay:

    Article Title: Wound healing potential of palm oil tocotrienols rich fraction
    Article Snippet: .. The serum was used for plasmaderived growth factor-BB, Platelet-derived growth factor -BB (E-EL-R0537-Elabscience) and Malondialdehyde, MDA (E-EL-0060-Elabscience) content testing using Elisa kit– based on manufacturer’s procedure (Elabscience, Texas, USA). eISSN: 2550-2166 © 2021 The Authors. ..



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    Autologous blood clot characteristics and secretome comparison between healthy control ( n = 12) and metabolic syndrome/diabetic (MetS/DM) ( n = 10) participants. (A) Representative image illustrating the blood clot in culture (that was spiked in with the respective treatments prior to clot induction) and its secretome. (B) The ratio of the initial clot size (surface area) and total protein (μg/mL) released into the clot secretome within the respective treatment groups. (C–D) Quantification <t>of</t> <t>PDGF‐BB</t> (pg/mL) (C), P‐selectin (pg/mL) (D) and CCL‐5 (pg/mL) levels within the clot secretome within the respective treatment groups. Statistical analysis: Two‐way ANOVA with Sidaks multiple comparisons test. * p < 0.05, ** p < 0.01.
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    Autologous blood clot characteristics and secretome comparison between healthy control ( n = 12) and metabolic syndrome/diabetic (MetS/DM) ( n = 10) participants. (A) Representative image illustrating the blood clot in culture (that was spiked in with the respective treatments prior to clot induction) and its secretome. (B) The ratio of the initial clot size (surface area) and total protein (μg/mL) released into the clot secretome within the respective treatment groups. (C–D) Quantification <t>of</t> <t>PDGF‐BB</t> (pg/mL) (C), P‐selectin (pg/mL) (D) and CCL‐5 (pg/mL) levels within the clot secretome within the respective treatment groups. Statistical analysis: Two‐way ANOVA with Sidaks multiple comparisons test. * p < 0.05, ** p < 0.01.
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    Autologous blood clot characteristics and secretome comparison between healthy control ( n = 12) and metabolic syndrome/diabetic (MetS/DM) ( n = 10) participants. (A) Representative image illustrating the blood clot in culture (that was spiked in with the respective treatments prior to clot induction) and its secretome. (B) The ratio of the initial clot size (surface area) and total protein (μg/mL) released into the clot secretome within the respective treatment groups. (C–D) Quantification <t>of</t> <t>PDGF‐BB</t> (pg/mL) (C), P‐selectin (pg/mL) (D) and CCL‐5 (pg/mL) levels within the clot secretome within the respective treatment groups. Statistical analysis: Two‐way ANOVA with Sidaks multiple comparisons test. * p < 0.05, ** p < 0.01.
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    Autologous blood clot characteristics and secretome comparison between healthy control ( n = 12) and metabolic syndrome/diabetic (MetS/DM) ( n = 10) participants. (A) Representative image illustrating the blood clot in culture (that was spiked in with the respective treatments prior to clot induction) and its secretome. (B) The ratio of the initial clot size (surface area) and total protein (μg/mL) released into the clot secretome within the respective treatment groups. (C–D) Quantification <t>of</t> <t>PDGF‐BB</t> (pg/mL) (C), P‐selectin (pg/mL) (D) and CCL‐5 (pg/mL) levels within the clot secretome within the respective treatment groups. Statistical analysis: Two‐way ANOVA with Sidaks multiple comparisons test. * p < 0.05, ** p < 0.01.
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    Autologous blood clot characteristics and secretome comparison between healthy control ( n = 12) and metabolic syndrome/diabetic (MetS/DM) ( n = 10) participants. (A) Representative image illustrating the blood clot in culture (that was spiked in with the respective treatments prior to clot induction) and its secretome. (B) The ratio of the initial clot size (surface area) and total protein (μg/mL) released into the clot secretome within the respective treatment groups. (C–D) Quantification <t>of</t> <t>PDGF‐BB</t> (pg/mL) (C), P‐selectin (pg/mL) (D) and CCL‐5 (pg/mL) levels within the clot secretome within the respective treatment groups. Statistical analysis: Two‐way ANOVA with Sidaks multiple comparisons test. * p < 0.05, ** p < 0.01.
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    Image Search Results


    Autologous blood clot characteristics and secretome comparison between healthy control ( n = 12) and metabolic syndrome/diabetic (MetS/DM) ( n = 10) participants. (A) Representative image illustrating the blood clot in culture (that was spiked in with the respective treatments prior to clot induction) and its secretome. (B) The ratio of the initial clot size (surface area) and total protein (μg/mL) released into the clot secretome within the respective treatment groups. (C–D) Quantification of PDGF‐BB (pg/mL) (C), P‐selectin (pg/mL) (D) and CCL‐5 (pg/mL) levels within the clot secretome within the respective treatment groups. Statistical analysis: Two‐way ANOVA with Sidaks multiple comparisons test. * p < 0.05, ** p < 0.01.

    Journal: Wound Repair and Regeneration

    Article Title: Autologous Blood Clot Therapy for Wounds: Investigating the Chemotactic Effect on PBMCs and Fibroblasts in Diabetes

    doi: 10.1111/wrr.70153

    Figure Lengend Snippet: Autologous blood clot characteristics and secretome comparison between healthy control ( n = 12) and metabolic syndrome/diabetic (MetS/DM) ( n = 10) participants. (A) Representative image illustrating the blood clot in culture (that was spiked in with the respective treatments prior to clot induction) and its secretome. (B) The ratio of the initial clot size (surface area) and total protein (μg/mL) released into the clot secretome within the respective treatment groups. (C–D) Quantification of PDGF‐BB (pg/mL) (C), P‐selectin (pg/mL) (D) and CCL‐5 (pg/mL) levels within the clot secretome within the respective treatment groups. Statistical analysis: Two‐way ANOVA with Sidaks multiple comparisons test. * p < 0.05, ** p < 0.01.

    Article Snippet: The concentrations of platelet‐derived growth factor‐BB (PDGF‐BB) (E‐EL‐H1577, Elabscience, USA), P‐selectin (SEA569Hu; Cloud‐Clone Corp, USA) and CCL‐5 (Proteintech, USA) were determined using sandwich ELISA assays and the absorbance read at 450 nm using a microplate reader (Multiskan GO 1.00.40; Thermo‐Scientific Group, USA) according to the manufacturer's instructions.

    Techniques: Comparison, Control