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well elisa plates  (Thermo Fisher)


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    Structured Review

    Thermo Fisher well elisa plates
    Well Elisa Plates, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/elisa+plates/TMB+QUICK%2C+for+ELISA%2C+Liquid+Substrate/pm42143412-63-4-18
    Average 95 stars, based on 1 article reviews
    well elisa plates - by Bioz Stars, 2026-10
    95/100 stars

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    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: Regulation of immune responses to therapeutic factor VIII by transplacental delivery of Fc-fused immunodominant factor VIII domains or peptides.
    Article Snippet: .. In the case of rFVIIIFc and rFVIIIFc mutants, ELISA plates (Thermo Scientific) were coated with GMA-8015 (antiA2 domain, Green Mountain, Burlington, VT) and GMA-8026 (anti-C2 domain, Green Mountain) at 1 μg/ml in PBS overnight at 4°C. .. After the addition of plasma, bound FVIII was revealed using a biotinylated sheep polyclonal anti-FVIII antibody (SAF8C, Stago, Asnières-sur-Seine, France), followed by streptavidin coupled to horseradish peroxidase (HRP).

    Article Title: Hepatitis B antibodies
    Article Snippet: .. Briefly, ELISA plates (Thermo Scientific, Cat #15031) were coated with 5 μg/ml horse polyclonal-HBsAg capture antibody (MyBiosource, Cat #MBS315002) for 2 hours at 37° C., then blocked overnight at 4° C. with 5% milk. ..

    Article Title: An Antibody Biomarker Associated with Onchocerca volvulus Microfilariae Identified by Proteomic Analysis of Parasite Tissues Isolated from Paraffin Embedded O. volvulus Nodules by Laser Capture Microdissection.
    Article Snippet: .. We coated 96 well round bottom ELISA plates (Immunlon 2 HB, ThermoFischer Scientific, Waltham, MA) with 100 mL of OVOC12404 antigen diluted to 2 mg/ml in 0.06 M carbonate buffer pH 9.6 and incubated the plates overnight at 37 C in a humidified chamber. ..

    Article Title: IRF7 controls spontaneous autoimmune germinal center and plasma cell checkpoints.
    Article Snippet: How IRF7 promotes autoimmune B cell responses and systemic autoimmunity is unclear.. Analysis of spontaneous SLE-prone mice deficient in IRF7 uncovered the IRF7 role in regulating autoimmune germinal center (GC), plasma cell (PC), and autoantibody responses and disease.. IRF7, however, was dispensable for foreign antigen–driven GC, PC, and antibody responses.

    Article Title: LetA defines a structurally distinct transporter family involved in lipid trafficking
    Article Snippet: .. For ELISA, purified LetA or negative control protein streptavidin diluted in LetA storage buffer (20 mM Tris, pH8, 150 mM NaCl, 10% glycerol, 0.5 mM DDM) were coated (50 ng/well) on ELISA plates (Thermo Fisher Scientific, 464718) following the manufacturer’s instructions. ..

    Article Title: A universal design of restructured dimer antigens: development of a superior vaccine against the Newcastle disease virus in transgenic rice
    Article Snippet: Unconjugated peptides were removed by purification using a desalting column (Thermo), and the conjugated peptides were stored at - 80 °C. .. For the ELISA assay, ELISA plates (Thermo) were coated overnight with BSA-peptide at a concentration of 100 ng/well, while BSA alone served as the negative control. ..

    other:

    Article Title: Kinetically activating nanovaccine mimicking multidimensional immunomodulation of natural infection for broad protection against heterologous viruses in animal models
    Article Snippet: All procedures, including immunisation, blood collections and euthanasia, were performed under anaesthesia using xylazine (UNIBIOtech, cat. no. 326R02, Gyeonggido, Korea) and alfaxalone (Jurox, cat. no. 520635, Rutherford, Australia).

    Article Title: Kinetically activating nanovaccine mimicking multidimensional immunomodulation of natural infection for broad protection against heterologous viruses in animal models.
    Article Snippet: The sera from each group were added to the antigen-coated plates, followed by incubation with HRP-antimouse IgG (Abcam, cat. no. ab97023, USA).

    Incubation:

    Article Title: An Antibody Biomarker Associated with Onchocerca volvulus Microfilariae Identified by Proteomic Analysis of Parasite Tissues Isolated from Paraffin Embedded O. volvulus Nodules by Laser Capture Microdissection.
    Article Snippet: .. We coated 96 well round bottom ELISA plates (Immunlon 2 HB, ThermoFischer Scientific, Waltham, MA) with 100 mL of OVOC12404 antigen diluted to 2 mg/ml in 0.06 M carbonate buffer pH 9.6 and incubated the plates overnight at 37 C in a humidified chamber. ..

    Purification:

    Article Title: LetA defines a structurally distinct transporter family involved in lipid trafficking
    Article Snippet: .. For ELISA, purified LetA or negative control protein streptavidin diluted in LetA storage buffer (20 mM Tris, pH8, 150 mM NaCl, 10% glycerol, 0.5 mM DDM) were coated (50 ng/well) on ELISA plates (Thermo Fisher Scientific, 464718) following the manufacturer’s instructions. ..

    Negative Control:

    Article Title: LetA defines a structurally distinct transporter family involved in lipid trafficking
    Article Snippet: .. For ELISA, purified LetA or negative control protein streptavidin diluted in LetA storage buffer (20 mM Tris, pH8, 150 mM NaCl, 10% glycerol, 0.5 mM DDM) were coated (50 ng/well) on ELISA plates (Thermo Fisher Scientific, 464718) following the manufacturer’s instructions. ..

    Article Title: A universal design of restructured dimer antigens: development of a superior vaccine against the Newcastle disease virus in transgenic rice
    Article Snippet: Unconjugated peptides were removed by purification using a desalting column (Thermo), and the conjugated peptides were stored at - 80 °C. .. For the ELISA assay, ELISA plates (Thermo) were coated overnight with BSA-peptide at a concentration of 100 ng/well, while BSA alone served as the negative control. ..

    Concentration Assay:

    Article Title: A universal design of restructured dimer antigens: development of a superior vaccine against the Newcastle disease virus in transgenic rice
    Article Snippet: Unconjugated peptides were removed by purification using a desalting column (Thermo), and the conjugated peptides were stored at - 80 °C. .. For the ELISA assay, ELISA plates (Thermo) were coated overnight with BSA-peptide at a concentration of 100 ng/well, while BSA alone served as the negative control. ..



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    (A) Sera from MRL lpr mice (n=12, bled weekly from 8 to 13 weeks of age) were analyzed by <t>ELISA</t> using synthetic 10×RG peptides: native sequence (GRGRGRGRGRGRGRGRGRGR) vs. SDMA-modified (lowercase ‘r’ denotes SDMA; GrGrGrGRGRGrGrGrGRGR). All 12 mice developed anti SDMA antibody titers above the corresponding native controls, and the majority (9/12) showed a gradual increase in anti-SDMA titers over time. (B) Immunoblotting of HEp-2 lysates revealed progressive changes in band patterns from 10 weeks onward. To identify SDMA specific reactive proteins, cells were pretreated with the methyltransferase inhibitor EPZ015666 (EPZ) before lysis. A prominent ∼15 kDa band (arrowhead) was markedly reduced by EPZ pretreatment, supporting its recognition by anti SDMA antibodies. (C) Sera from three 12 week old MRL lpr littermates (Lpr 1, 2, 3) each showed distinct band patterns against the cell lysates. EPZ pretreatment of the cells reduced the intensity of several bands in all three mice. (D) Workflow for isolating hybridoma clones from individual plasma cells to obtain monoclonal antibodies (mAbs) specific for SDMA. MRL lpr mice were not immunized with any antigen; thus, the resulting mAbs represent naturally arising autoantibodies. (E) Two antibody clones were tested against the native versus SDMA peptide array shown in Figurè3. Clone P4A2F4 reacted extensively with most SDMA containing peptides, whereas clone P2C1C10 showed no reactivity. (F) The two mAbs produced different band patterns on cell lysates. P4A2F4 recognized bands that were reduced in EPZ pretreated lysates, consistent with SDMA specificity. (G) After implantation of the SDMA-reactive hybridoma clone into the peritoneal cavity of healthy BALB/c mice, the kidneys showed extensive IgG deposition, reminiscent of human lupus nephritis.
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    (A) Sera from MRL lpr mice (n=12, bled weekly from 8 to 13 weeks of age) were analyzed by <t>ELISA</t> using synthetic 10×RG peptides: native sequence (GRGRGRGRGRGRGRGRGRGR) vs. SDMA-modified (lowercase ‘r’ denotes SDMA; GrGrGrGRGRGrGrGrGRGR). All 12 mice developed anti SDMA antibody titers above the corresponding native controls, and the majority (9/12) showed a gradual increase in anti-SDMA titers over time. (B) Immunoblotting of HEp-2 lysates revealed progressive changes in band patterns from 10 weeks onward. To identify SDMA specific reactive proteins, cells were pretreated with the methyltransferase inhibitor EPZ015666 (EPZ) before lysis. A prominent ∼15 kDa band (arrowhead) was markedly reduced by EPZ pretreatment, supporting its recognition by anti SDMA antibodies. (C) Sera from three 12 week old MRL lpr littermates (Lpr 1, 2, 3) each showed distinct band patterns against the cell lysates. EPZ pretreatment of the cells reduced the intensity of several bands in all three mice. (D) Workflow for isolating hybridoma clones from individual plasma cells to obtain monoclonal antibodies (mAbs) specific for SDMA. MRL lpr mice were not immunized with any antigen; thus, the resulting mAbs represent naturally arising autoantibodies. (E) Two antibody clones were tested against the native versus SDMA peptide array shown in Figurè3. Clone P4A2F4 reacted extensively with most SDMA containing peptides, whereas clone P2C1C10 showed no reactivity. (F) The two mAbs produced different band patterns on cell lysates. P4A2F4 recognized bands that were reduced in EPZ pretreated lysates, consistent with SDMA specificity. (G) After implantation of the SDMA-reactive hybridoma clone into the peritoneal cavity of healthy BALB/c mice, the kidneys showed extensive IgG deposition, reminiscent of human lupus nephritis.
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    (A) Sera from MRL lpr mice (n=12, bled weekly from 8 to 13 weeks of age) were analyzed by <t>ELISA</t> using synthetic 10×RG peptides: native sequence (GRGRGRGRGRGRGRGRGRGR) vs. SDMA-modified (lowercase ‘r’ denotes SDMA; GrGrGrGRGRGrGrGrGRGR). All 12 mice developed anti SDMA antibody titers above the corresponding native controls, and the majority (9/12) showed a gradual increase in anti-SDMA titers over time. (B) Immunoblotting of HEp-2 lysates revealed progressive changes in band patterns from 10 weeks onward. To identify SDMA specific reactive proteins, cells were pretreated with the methyltransferase inhibitor EPZ015666 (EPZ) before lysis. A prominent ∼15 kDa band (arrowhead) was markedly reduced by EPZ pretreatment, supporting its recognition by anti SDMA antibodies. (C) Sera from three 12 week old MRL lpr littermates (Lpr 1, 2, 3) each showed distinct band patterns against the cell lysates. EPZ pretreatment of the cells reduced the intensity of several bands in all three mice. (D) Workflow for isolating hybridoma clones from individual plasma cells to obtain monoclonal antibodies (mAbs) specific for SDMA. MRL lpr mice were not immunized with any antigen; thus, the resulting mAbs represent naturally arising autoantibodies. (E) Two antibody clones were tested against the native versus SDMA peptide array shown in Figurè3. Clone P4A2F4 reacted extensively with most SDMA containing peptides, whereas clone P2C1C10 showed no reactivity. (F) The two mAbs produced different band patterns on cell lysates. P4A2F4 recognized bands that were reduced in EPZ pretreated lysates, consistent with SDMA specificity. (G) After implantation of the SDMA-reactive hybridoma clone into the peritoneal cavity of healthy BALB/c mice, the kidneys showed extensive IgG deposition, reminiscent of human lupus nephritis.
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    (A) Sera from MRL lpr mice (n=12, bled weekly from 8 to 13 weeks of age) were analyzed by <t>ELISA</t> using synthetic 10×RG peptides: native sequence (GRGRGRGRGRGRGRGRGRGR) vs. SDMA-modified (lowercase ‘r’ denotes SDMA; GrGrGrGRGRGrGrGrGRGR). All 12 mice developed anti SDMA antibody titers above the corresponding native controls, and the majority (9/12) showed a gradual increase in anti-SDMA titers over time. (B) Immunoblotting of HEp-2 lysates revealed progressive changes in band patterns from 10 weeks onward. To identify SDMA specific reactive proteins, cells were pretreated with the methyltransferase inhibitor EPZ015666 (EPZ) before lysis. A prominent ∼15 kDa band (arrowhead) was markedly reduced by EPZ pretreatment, supporting its recognition by anti SDMA antibodies. (C) Sera from three 12 week old MRL lpr littermates (Lpr 1, 2, 3) each showed distinct band patterns against the cell lysates. EPZ pretreatment of the cells reduced the intensity of several bands in all three mice. (D) Workflow for isolating hybridoma clones from individual plasma cells to obtain monoclonal antibodies (mAbs) specific for SDMA. MRL lpr mice were not immunized with any antigen; thus, the resulting mAbs represent naturally arising autoantibodies. (E) Two antibody clones were tested against the native versus SDMA peptide array shown in Figurè3. Clone P4A2F4 reacted extensively with most SDMA containing peptides, whereas clone P2C1C10 showed no reactivity. (F) The two mAbs produced different band patterns on cell lysates. P4A2F4 recognized bands that were reduced in EPZ pretreated lysates, consistent with SDMA specificity. (G) After implantation of the SDMA-reactive hybridoma clone into the peritoneal cavity of healthy BALB/c mice, the kidneys showed extensive IgG deposition, reminiscent of human lupus nephritis.
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    Gold Standard Diagnostics abraxis glyphosate plate elisa kit
    <t>Glyphosate</t> level in serum in study groups (mean±SEM). ECLH: Low-grade and High-grade endometrial cancer (n = 32); ECL: Low-grade endometrial cancer (n = 22); EIN: Endometrial intraepithelial neoplasia (n = 4) and C: control (n = 32). Glyphosateconcentration concentration in serum, measured in ECLH, ECL, EIN and C groups. *ECLH serum level significantly differs from control serum level; GLY serum: ECLH serum 0.1829 ± 0.0272 ng/ml; ECL serum 0.2148 ± 0.0406 ng/ml; EIN serum 0.1938 ± 0.00488 ng/ml and C serum 0.1297 ± 0.0167 ng/ml.
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    Thermo Fisher well elisa plates
    <t>Glyphosate</t> level in serum in study groups (mean±SEM). ECLH: Low-grade and High-grade endometrial cancer (n = 32); ECL: Low-grade endometrial cancer (n = 22); EIN: Endometrial intraepithelial neoplasia (n = 4) and C: control (n = 32). Glyphosateconcentration concentration in serum, measured in ECLH, ECL, EIN and C groups. *ECLH serum level significantly differs from control serum level; GLY serum: ECLH serum 0.1829 ± 0.0272 ng/ml; ECL serum 0.2148 ± 0.0406 ng/ml; EIN serum 0.1938 ± 0.00488 ng/ml and C serum 0.1297 ± 0.0167 ng/ml.
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    Qiagen ni nta elisa plate
    <t>Glyphosate</t> level in serum in study groups (mean±SEM). ECLH: Low-grade and High-grade endometrial cancer (n = 32); ECL: Low-grade endometrial cancer (n = 22); EIN: Endometrial intraepithelial neoplasia (n = 4) and C: control (n = 32). Glyphosateconcentration concentration in serum, measured in ECLH, ECL, EIN and C groups. *ECLH serum level significantly differs from control serum level; GLY serum: ECLH serum 0.1829 ± 0.0272 ng/ml; ECL serum 0.2148 ± 0.0406 ng/ml; EIN serum 0.1938 ± 0.00488 ng/ml and C serum 0.1297 ± 0.0167 ng/ml.
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    Image Search Results


    (A) Sera from MRL lpr mice (n=12, bled weekly from 8 to 13 weeks of age) were analyzed by ELISA using synthetic 10×RG peptides: native sequence (GRGRGRGRGRGRGRGRGRGR) vs. SDMA-modified (lowercase ‘r’ denotes SDMA; GrGrGrGRGRGrGrGrGRGR). All 12 mice developed anti SDMA antibody titers above the corresponding native controls, and the majority (9/12) showed a gradual increase in anti-SDMA titers over time. (B) Immunoblotting of HEp-2 lysates revealed progressive changes in band patterns from 10 weeks onward. To identify SDMA specific reactive proteins, cells were pretreated with the methyltransferase inhibitor EPZ015666 (EPZ) before lysis. A prominent ∼15 kDa band (arrowhead) was markedly reduced by EPZ pretreatment, supporting its recognition by anti SDMA antibodies. (C) Sera from three 12 week old MRL lpr littermates (Lpr 1, 2, 3) each showed distinct band patterns against the cell lysates. EPZ pretreatment of the cells reduced the intensity of several bands in all three mice. (D) Workflow for isolating hybridoma clones from individual plasma cells to obtain monoclonal antibodies (mAbs) specific for SDMA. MRL lpr mice were not immunized with any antigen; thus, the resulting mAbs represent naturally arising autoantibodies. (E) Two antibody clones were tested against the native versus SDMA peptide array shown in Figurè3. Clone P4A2F4 reacted extensively with most SDMA containing peptides, whereas clone P2C1C10 showed no reactivity. (F) The two mAbs produced different band patterns on cell lysates. P4A2F4 recognized bands that were reduced in EPZ pretreated lysates, consistent with SDMA specificity. (G) After implantation of the SDMA-reactive hybridoma clone into the peritoneal cavity of healthy BALB/c mice, the kidneys showed extensive IgG deposition, reminiscent of human lupus nephritis.

    Journal: bioRxiv

    Article Title: Symmetric Dimethylarginine Modification Drives Shared and Divergent Antigen Reactivity in Lupus

    doi: 10.64898/2026.09.22.753525

    Figure Lengend Snippet: (A) Sera from MRL lpr mice (n=12, bled weekly from 8 to 13 weeks of age) were analyzed by ELISA using synthetic 10×RG peptides: native sequence (GRGRGRGRGRGRGRGRGRGR) vs. SDMA-modified (lowercase ‘r’ denotes SDMA; GrGrGrGRGRGrGrGrGRGR). All 12 mice developed anti SDMA antibody titers above the corresponding native controls, and the majority (9/12) showed a gradual increase in anti-SDMA titers over time. (B) Immunoblotting of HEp-2 lysates revealed progressive changes in band patterns from 10 weeks onward. To identify SDMA specific reactive proteins, cells were pretreated with the methyltransferase inhibitor EPZ015666 (EPZ) before lysis. A prominent ∼15 kDa band (arrowhead) was markedly reduced by EPZ pretreatment, supporting its recognition by anti SDMA antibodies. (C) Sera from three 12 week old MRL lpr littermates (Lpr 1, 2, 3) each showed distinct band patterns against the cell lysates. EPZ pretreatment of the cells reduced the intensity of several bands in all three mice. (D) Workflow for isolating hybridoma clones from individual plasma cells to obtain monoclonal antibodies (mAbs) specific for SDMA. MRL lpr mice were not immunized with any antigen; thus, the resulting mAbs represent naturally arising autoantibodies. (E) Two antibody clones were tested against the native versus SDMA peptide array shown in Figurè3. Clone P4A2F4 reacted extensively with most SDMA containing peptides, whereas clone P2C1C10 showed no reactivity. (F) The two mAbs produced different band patterns on cell lysates. P4A2F4 recognized bands that were reduced in EPZ pretreated lysates, consistent with SDMA specificity. (G) After implantation of the SDMA-reactive hybridoma clone into the peritoneal cavity of healthy BALB/c mice, the kidneys showed extensive IgG deposition, reminiscent of human lupus nephritis.

    Article Snippet: High-binding ELISA plates (Greiner Bio-One, 655081) were coated with 250 ng/well of streptavidin (Leinco Technologies, S203) overnight at 4°C.

    Techniques: Enzyme-linked Immunosorbent Assay, Sequencing, Modification, Western Blot, Lysis, Clone Assay, Clinical Proteomics, Bioprocessing, Autoantibodies, Peptide Microarray, Produced

    Glyphosate level in serum in study groups (mean±SEM). ECLH: Low-grade and High-grade endometrial cancer (n = 32); ECL: Low-grade endometrial cancer (n = 22); EIN: Endometrial intraepithelial neoplasia (n = 4) and C: control (n = 32). Glyphosateconcentration concentration in serum, measured in ECLH, ECL, EIN and C groups. *ECLH serum level significantly differs from control serum level; GLY serum: ECLH serum 0.1829 ± 0.0272 ng/ml; ECL serum 0.2148 ± 0.0406 ng/ml; EIN serum 0.1938 ± 0.00488 ng/ml and C serum 0.1297 ± 0.0167 ng/ml.

    Journal: Toxicology Reports

    Article Title: Presence of glyphosate in endometrial cancer tissue: A cross-sectional study

    doi: 10.1016/j.toxrep.2026.102255

    Figure Lengend Snippet: Glyphosate level in serum in study groups (mean±SEM). ECLH: Low-grade and High-grade endometrial cancer (n = 32); ECL: Low-grade endometrial cancer (n = 22); EIN: Endometrial intraepithelial neoplasia (n = 4) and C: control (n = 32). Glyphosateconcentration concentration in serum, measured in ECLH, ECL, EIN and C groups. *ECLH serum level significantly differs from control serum level; GLY serum: ECLH serum 0.1829 ± 0.0272 ng/ml; ECL serum 0.2148 ± 0.0406 ng/ml; EIN serum 0.1938 ± 0.00488 ng/ml and C serum 0.1297 ± 0.0167 ng/ml.

    Article Snippet: A commercial kit (ABRAXIS Glyphosate Plate ELISA Kit, PN 500205, Gold Standard Diagnostics, Warminster, US) was used in this study.

    Techniques: Control, Concentration Assay

    Glyphosate level in endometrial tissue in study groups (mean±SEM). ECLH: Low-grade and High-grade endometrial cancer (n = 32); ECL: Low-grade endometrial cancer (n = 22); EIN: Endometrial intraepithelial neoplasia (n = 4) and C: control (n = 32). GlyphosateconcentrationGLY concentration in endometrial tissue, measured in ECLH, ECL, EIN and C groups. We adjusted the mean concentration values for the endometrium by applying a serum density value of 1.025 g/ml as a conversion factor: from pg/ml to pg/g and ng/ml to ng/g. *ECLH endometrium level shows a significant difference from the control serum level; GLY endometrium: ECLH endometrium 0.4174 ± 0.3461 ng/g; ECL endometrium 0.4073 ± 0.04162 ng/g; EIN endometrium 0.3798 ± 0.09556 ng/g and C endometrium 0.318 ± 0.0251 ng/g.

    Journal: Toxicology Reports

    Article Title: Presence of glyphosate in endometrial cancer tissue: A cross-sectional study

    doi: 10.1016/j.toxrep.2026.102255

    Figure Lengend Snippet: Glyphosate level in endometrial tissue in study groups (mean±SEM). ECLH: Low-grade and High-grade endometrial cancer (n = 32); ECL: Low-grade endometrial cancer (n = 22); EIN: Endometrial intraepithelial neoplasia (n = 4) and C: control (n = 32). GlyphosateconcentrationGLY concentration in endometrial tissue, measured in ECLH, ECL, EIN and C groups. We adjusted the mean concentration values for the endometrium by applying a serum density value of 1.025 g/ml as a conversion factor: from pg/ml to pg/g and ng/ml to ng/g. *ECLH endometrium level shows a significant difference from the control serum level; GLY endometrium: ECLH endometrium 0.4174 ± 0.3461 ng/g; ECL endometrium 0.4073 ± 0.04162 ng/g; EIN endometrium 0.3798 ± 0.09556 ng/g and C endometrium 0.318 ± 0.0251 ng/g.

    Article Snippet: A commercial kit (ABRAXIS Glyphosate Plate ELISA Kit, PN 500205, Gold Standard Diagnostics, Warminster, US) was used in this study.

    Techniques: Control, Concentration Assay

    Glyphosate level in serum and endometrial tissue in study groups (mean±SEM). ECLH: Low-grade and High-grade endometrial cancer (n = 32); ECL: Low-grade endometrial cancer (n = 22); and C: control (n = 32). Glyphosateconcentration concentration in endometrial tissue, measured in ECLH, ECL, and C groups. We converted concentration mean values in the case of endometriumendometrium using 1025 g/ml serum density value as a multiplier: pg/ml to pg/g, ng/ml to ng/g. *Endometrium level significantly differs from control serum level in all study groups. P < 0.0001; GLY levels: ECLH serum 0.1829 ± 0.0272 ng/ml; endometrium 0.4174 ± 0.3461 ng/g; ECL serum 0.2148 ± 0.0406 ng/ml; endometrium 0.4073 ± 0.04162 ng/g; and C serum 0.1297 ± 0.0167 ng/ml; endometrium 0.318 ± 0.0251 ng/g.

    Journal: Toxicology Reports

    Article Title: Presence of glyphosate in endometrial cancer tissue: A cross-sectional study

    doi: 10.1016/j.toxrep.2026.102255

    Figure Lengend Snippet: Glyphosate level in serum and endometrial tissue in study groups (mean±SEM). ECLH: Low-grade and High-grade endometrial cancer (n = 32); ECL: Low-grade endometrial cancer (n = 22); and C: control (n = 32). Glyphosateconcentration concentration in endometrial tissue, measured in ECLH, ECL, and C groups. We converted concentration mean values in the case of endometriumendometrium using 1025 g/ml serum density value as a multiplier: pg/ml to pg/g, ng/ml to ng/g. *Endometrium level significantly differs from control serum level in all study groups. P < 0.0001; GLY levels: ECLH serum 0.1829 ± 0.0272 ng/ml; endometrium 0.4174 ± 0.3461 ng/g; ECL serum 0.2148 ± 0.0406 ng/ml; endometrium 0.4073 ± 0.04162 ng/g; and C serum 0.1297 ± 0.0167 ng/ml; endometrium 0.318 ± 0.0251 ng/g.

    Article Snippet: A commercial kit (ABRAXIS Glyphosate Plate ELISA Kit, PN 500205, Gold Standard Diagnostics, Warminster, US) was used in this study.

    Techniques: Control, Concentration Assay