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recombinant human serum albumin  (ACROBiosystems)


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    Structured Review

    ACROBiosystems recombinant human serum albumin
    (A) Platelets (green) adhered exclusively to the albumin-adsorbed region (magenta), but not to the casein-adsorbed region (dark). Albumin was pre-labeled with Alexa488. Platelets were stained with phalloidin to label F-actin. (B) Resting platelets, ADP-activated platelets and HeLa cells on fibronectin (FN), fibrinogen (Fg), bovine serum albumin (BSA), human serum albumin (HSA), <t>recombinant</t> human serum albumin (rHSA) and casein-adsorbed glass surfaces, respectively. ( C-E ) Cell spreading areas of platelets or HeLa cells on the six surfaces. Platelets in (C) were kept at a resting state prior to cell plating, whereas platelets in (D) were pre-activated by 10 µM ADP. (**** P <0.0001; ns P >0.05; Each data point represents one cell; For each condition, N = 100 cells from three independent experiments; Error bars indicate SD).
    Recombinant Human Serum Albumin, supplied by ACROBiosystems, used in various techniques. Bioz Stars score: 95/100, based on 18 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+serum+albumin+protein+hsa/Human+Serum+Albumin+Protein%2C+His+Tag/bio_rxiv__64898__2026__03__30__715112-168-48-53
    Average 95 stars, based on 18 article reviews
    recombinant human serum albumin - by Bioz Stars, 2026-09
    95/100 stars

    Images

    1) Product Images from "Denatured Albumin Gains a Function of Regulating Platelet Activity"

    Article Title: Denatured Albumin Gains a Function of Regulating Platelet Activity

    Journal: bioRxiv

    doi: 10.64898/2026.03.30.715112

    (A) Platelets (green) adhered exclusively to the albumin-adsorbed region (magenta), but not to the casein-adsorbed region (dark). Albumin was pre-labeled with Alexa488. Platelets were stained with phalloidin to label F-actin. (B) Resting platelets, ADP-activated platelets and HeLa cells on fibronectin (FN), fibrinogen (Fg), bovine serum albumin (BSA), human serum albumin (HSA), recombinant human serum albumin (rHSA) and casein-adsorbed glass surfaces, respectively. ( C-E ) Cell spreading areas of platelets or HeLa cells on the six surfaces. Platelets in (C) were kept at a resting state prior to cell plating, whereas platelets in (D) were pre-activated by 10 µM ADP. (**** P <0.0001; ns P >0.05; Each data point represents one cell; For each condition, N = 100 cells from three independent experiments; Error bars indicate SD).
    Figure Legend Snippet: (A) Platelets (green) adhered exclusively to the albumin-adsorbed region (magenta), but not to the casein-adsorbed region (dark). Albumin was pre-labeled with Alexa488. Platelets were stained with phalloidin to label F-actin. (B) Resting platelets, ADP-activated platelets and HeLa cells on fibronectin (FN), fibrinogen (Fg), bovine serum albumin (BSA), human serum albumin (HSA), recombinant human serum albumin (rHSA) and casein-adsorbed glass surfaces, respectively. ( C-E ) Cell spreading areas of platelets or HeLa cells on the six surfaces. Platelets in (C) were kept at a resting state prior to cell plating, whereas platelets in (D) were pre-activated by 10 µM ADP. (**** P <0.0001; ns P >0.05; Each data point represents one cell; For each condition, N = 100 cells from three independent experiments; Error bars indicate SD).

    Techniques Used: Labeling, Staining, Recombinant

    Related Articles

    Modification:

    Article Title: Impedimetric Detection of Cancer Markers Based on Nanofiber Copolymers
    Article Snippet: Folic acid (FA) 98% was purchased from Loba Chemie PVT.LTD-Mumbai, India.Folic acid (FA) 98% was purchased from Loba Chemie PVT.LTD-Mumbai, India.. The Human FOLR2 Protein (FRs) > 90% (Mw = 26.5 KDa) and Human Serum Albumin Protein (HSA) > 95% (Mw = 67.4 KDa) were purchased from ACRO Biosystems, Newark, DE, USA.. The polyethylene oxide (PEO) (Mw = 600,000 Da), bovine serum albumin (BSA) < 96% (agarose gel electrophoresis), human plasma, Tris-HCl buffer, potassium chloride, and potassium ferricyanide/potassium ferrocyanide were purchased from Sigma-Aldrich Co. (St. Louis, MO, USA).The polyethylene oxide (PEO) (Mw = 600,000 Da), bovine serum albumin (BSA) < 96% (agarose gel electrophoresis), human plasma, Tris-HCl buffer, potassium chloride, and potassium ferricyanide/potassium ferrocyanide were purchased from Sigma-Aldrich Co. (St. Louis, MO, USA).

    Incubation:

    Article Title: Impedimetric Detection of Cancer Markers Based on Nanofiber Copolymers
    Article Snippet: Folic acid (FA) 98% was purchased from Loba Chemie PVT.LTD-Mumbai, India.Folic acid (FA) 98% was purchased from Loba Chemie PVT.LTD-Mumbai, India.. The Human FOLR2 Protein (FRs) > 90% (Mw = 26.5 KDa) and Human Serum Albumin Protein (HSA) > 95% (Mw = 67.4 KDa) were purchased from ACRO Biosystems, Newark, DE, USA.. The polyethylene oxide (PEO) (Mw = 600,000 Da), bovine serum albumin (BSA) < 96% (agarose gel electrophoresis), human plasma, Tris-HCl buffer, potassium chloride, and potassium ferricyanide/potassium ferrocyanide were purchased from Sigma-Aldrich Co. (St. Louis, MO, USA).The polyethylene oxide (PEO) (Mw = 600,000 Da), bovine serum albumin (BSA) < 96% (agarose gel electrophoresis), human plasma, Tris-HCl buffer, potassium chloride, and potassium ferricyanide/potassium ferrocyanide were purchased from Sigma-Aldrich Co. (St. Louis, MO, USA).



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    (A) Platelets (green) adhered exclusively to the albumin-adsorbed region (magenta), but not to the casein-adsorbed region (dark). Albumin was pre-labeled with Alexa488. Platelets were stained with phalloidin to label F-actin. (B) Resting platelets, ADP-activated platelets and HeLa cells on fibronectin (FN), fibrinogen (Fg), bovine serum albumin (BSA), human serum albumin (HSA), <t>recombinant</t> human serum albumin (rHSA) and casein-adsorbed glass surfaces, respectively. ( C-E ) Cell spreading areas of platelets or HeLa cells on the six surfaces. Platelets in (C) were kept at a resting state prior to cell plating, whereas platelets in (D) were pre-activated by 10 µM ADP. (**** P <0.0001; ns P >0.05; Each data point represents one cell; For each condition, N = 100 cells from three independent experiments; Error bars indicate SD).
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    Image Search Results


    (A) Platelets (green) adhered exclusively to the albumin-adsorbed region (magenta), but not to the casein-adsorbed region (dark). Albumin was pre-labeled with Alexa488. Platelets were stained with phalloidin to label F-actin. (B) Resting platelets, ADP-activated platelets and HeLa cells on fibronectin (FN), fibrinogen (Fg), bovine serum albumin (BSA), human serum albumin (HSA), recombinant human serum albumin (rHSA) and casein-adsorbed glass surfaces, respectively. ( C-E ) Cell spreading areas of platelets or HeLa cells on the six surfaces. Platelets in (C) were kept at a resting state prior to cell plating, whereas platelets in (D) were pre-activated by 10 µM ADP. (**** P <0.0001; ns P >0.05; Each data point represents one cell; For each condition, N = 100 cells from three independent experiments; Error bars indicate SD).

    Journal: bioRxiv

    Article Title: Denatured Albumin Gains a Function of Regulating Platelet Activity

    doi: 10.64898/2026.03.30.715112

    Figure Lengend Snippet: (A) Platelets (green) adhered exclusively to the albumin-adsorbed region (magenta), but not to the casein-adsorbed region (dark). Albumin was pre-labeled with Alexa488. Platelets were stained with phalloidin to label F-actin. (B) Resting platelets, ADP-activated platelets and HeLa cells on fibronectin (FN), fibrinogen (Fg), bovine serum albumin (BSA), human serum albumin (HSA), recombinant human serum albumin (rHSA) and casein-adsorbed glass surfaces, respectively. ( C-E ) Cell spreading areas of platelets or HeLa cells on the six surfaces. Platelets in (C) were kept at a resting state prior to cell plating, whereas platelets in (D) were pre-activated by 10 µM ADP. (**** P <0.0001; ns P >0.05; Each data point represents one cell; For each condition, N = 100 cells from three independent experiments; Error bars indicate SD).

    Article Snippet: Activated platelets or resting platelets at concentration of 4.0 × 10 4 /μL were seeded onto glass coverslips pre-coated with 10 μg/ml fibronectin (F1141, Sigma-Aldrich), 100 μg/mL fibrinogen (F3879, Sigma-Aldrich), 100 μg/mL ultrapure bovine serum albumin (AM2616, Invitrogen), 100 μg/mL ultrapure human serum albumin (A8763, Sigma-Aldrich), 100 μg/mL recombinant human serum albumin (HSA-H5220, Acro Biosystems) or 100 μg/ml casein, and incubated at 37 °C in a cell incubator containing 5% CO2 for 30 minutes.

    Techniques: Labeling, Staining, Recombinant