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il 34 levels  (R&D Systems)


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    R&D Systems il 34 levels
    Il 34 Levels, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 19 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/il+34+levels/Human+IL-34+Quantikine+ELISA+Kit/pm40381116-47-10-17
    Average 93 stars, based on 19 article reviews
    il 34 levels - by Bioz Stars, 2026-09
    93/100 stars

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    Clinical Proteomics:

    Article Title: Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Axatilimab in Healthy Japanese Male Participants: Results from a Phase 1, Randomized, Double-Blind, Dose-Escalation Study.
    Article Snippet: Plasma samples were analyzed for axatilimab using a sandwich enzyme-linked immunosorbent assay (ELISA) with a lower limit of quantitation of 150 ng/mL and an upper limit of quantitation of 10,000 ng/mL. .. Exploratory PD endpoints included change from baseline in CSF-1 and IL-34 levels, assessed by commercially available ELISAs (R&D Systems, Minneapolis, Minnesota, USA; Human M-CSF and Human IL-34 Quantikine ELISA Kits), and change from baseline in circulating monocyte numbers (cluster of differentiation [CD]14/ CD16), assessed by flow cytometry. ..

    Article Title: Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Axatilimab in Healthy Japanese Male Participants: Results from a Phase 1, Randomized, Double-Blind, Dose-Escalation Study
    Article Snippet: Plasma samples were analyzed for axatilimab using a sandwich enzyme-linked immunosorbent assay (ELISA) with a lower limit of quantitation of 150 ng/mL and an upper limit of quantitation of 10,000 ng/mL. .. Exploratory PD endpoints included change from baseline in CSF-1 and IL-34 levels, assessed by commercially available ELISAs (R&D Systems, Minneapolis, Minnesota, USA; Human M-CSF and Human IL-34 Quantikine ELISA Kits), and change from baseline in circulating monocyte numbers (cluster of differentiation [CD]14/CD16), assessed by flow cytometry. ..

    Enzyme-linked Immunosorbent Assay:

    Article Title: Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Axatilimab in Healthy Japanese Male Participants: Results from a Phase 1, Randomized, Double-Blind, Dose-Escalation Study.
    Article Snippet: Plasma samples were analyzed for axatilimab using a sandwich enzyme-linked immunosorbent assay (ELISA) with a lower limit of quantitation of 150 ng/mL and an upper limit of quantitation of 10,000 ng/mL. .. Exploratory PD endpoints included change from baseline in CSF-1 and IL-34 levels, assessed by commercially available ELISAs (R&D Systems, Minneapolis, Minnesota, USA; Human M-CSF and Human IL-34 Quantikine ELISA Kits), and change from baseline in circulating monocyte numbers (cluster of differentiation [CD]14/ CD16), assessed by flow cytometry. ..

    Article Title: Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Axatilimab in Healthy Japanese Male Participants: Results from a Phase 1, Randomized, Double-Blind, Dose-Escalation Study
    Article Snippet: Plasma samples were analyzed for axatilimab using a sandwich enzyme-linked immunosorbent assay (ELISA) with a lower limit of quantitation of 150 ng/mL and an upper limit of quantitation of 10,000 ng/mL. .. Exploratory PD endpoints included change from baseline in CSF-1 and IL-34 levels, assessed by commercially available ELISAs (R&D Systems, Minneapolis, Minnesota, USA; Human M-CSF and Human IL-34 Quantikine ELISA Kits), and change from baseline in circulating monocyte numbers (cluster of differentiation [CD]14/CD16), assessed by flow cytometry. ..

    Flow Cytometry:

    Article Title: Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Axatilimab in Healthy Japanese Male Participants: Results from a Phase 1, Randomized, Double-Blind, Dose-Escalation Study.
    Article Snippet: Plasma samples were analyzed for axatilimab using a sandwich enzyme-linked immunosorbent assay (ELISA) with a lower limit of quantitation of 150 ng/mL and an upper limit of quantitation of 10,000 ng/mL. .. Exploratory PD endpoints included change from baseline in CSF-1 and IL-34 levels, assessed by commercially available ELISAs (R&D Systems, Minneapolis, Minnesota, USA; Human M-CSF and Human IL-34 Quantikine ELISA Kits), and change from baseline in circulating monocyte numbers (cluster of differentiation [CD]14/ CD16), assessed by flow cytometry. ..

    Article Title: Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Axatilimab in Healthy Japanese Male Participants: Results from a Phase 1, Randomized, Double-Blind, Dose-Escalation Study
    Article Snippet: Plasma samples were analyzed for axatilimab using a sandwich enzyme-linked immunosorbent assay (ELISA) with a lower limit of quantitation of 150 ng/mL and an upper limit of quantitation of 10,000 ng/mL. .. Exploratory PD endpoints included change from baseline in CSF-1 and IL-34 levels, assessed by commercially available ELISAs (R&D Systems, Minneapolis, Minnesota, USA; Human M-CSF and Human IL-34 Quantikine ELISA Kits), and change from baseline in circulating monocyte numbers (cluster of differentiation [CD]14/CD16), assessed by flow cytometry. ..



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    Image Search Results


    Results of logistic regression analysis on CSF-1 and IL-34 levels

    Journal: Journal of Periodontal & Implant Science

    Article Title: Gingival crevicular fluid CSF-1 and IL-34 levels in patients with stage III grade C periodontitis and uncontrolled type 2 diabetes mellitus

    doi: 10.5051/jpis.2106260313

    Figure Lengend Snippet: Results of logistic regression analysis on CSF-1 and IL-34 levels

    Article Snippet: CSF-1 and IL-34 levels in the GCF were calculated using enzyme-linked immunosorbent assay (ELISA) kits (Human CSF-1 ELISA kit and Human IL-34 ELISA kit; Elabscience, Houston, TX, USA) according to the manufacturer’s guidelines.

    Techniques:

    Protein expression of IL‐34 from human PTC samples. A, Western blot analysis of IL‐34 expression in PTC tissues, their adjacent noncancerous tissues, and normal controls. B, The ratio of IL‐34/GAPDH was determined to give a mean net density. C, Real‐time PCR analysis of IL‐34 expression in PTC tissues, their adjacent noncancerous tissues, and normal controls. Data were presented as the means ± standard error. ** P < .01 was considered significant

    Journal: Journal of Clinical Laboratory Analysis

    Article Title: IL‐34 is a potential biomarker for the treatment of papillary thyroid cancer

    doi: 10.1002/jcla.23335

    Figure Lengend Snippet: Protein expression of IL‐34 from human PTC samples. A, Western blot analysis of IL‐34 expression in PTC tissues, their adjacent noncancerous tissues, and normal controls. B, The ratio of IL‐34/GAPDH was determined to give a mean net density. C, Real‐time PCR analysis of IL‐34 expression in PTC tissues, their adjacent noncancerous tissues, and normal controls. Data were presented as the means ± standard error. ** P < .01 was considered significant

    Article Snippet: Serum IL‐34 levels were analyzed by ELISA assay (R&D Systems, Minneapolis, MN, USA).

    Techniques: Expressing, Western Blot, Real-time Polymerase Chain Reaction

    IL‐34 promotes proliferation on PTC cells. Cell proliferation was determined via the CCK‐8 assay to examine the proliferation of TPC‐1 (A) and K1 cells (B) in accordance to transfected with si‐NC or si‐IL‐34. Cell proliferation in TPC‐1 (C) and K1 cells (D) which were infected with lenti‐vector or lenti‐IL‐34. Data were presented as the means ± standard error. ** P < .01 was considered significant

    Journal: Journal of Clinical Laboratory Analysis

    Article Title: IL‐34 is a potential biomarker for the treatment of papillary thyroid cancer

    doi: 10.1002/jcla.23335

    Figure Lengend Snippet: IL‐34 promotes proliferation on PTC cells. Cell proliferation was determined via the CCK‐8 assay to examine the proliferation of TPC‐1 (A) and K1 cells (B) in accordance to transfected with si‐NC or si‐IL‐34. Cell proliferation in TPC‐1 (C) and K1 cells (D) which were infected with lenti‐vector or lenti‐IL‐34. Data were presented as the means ± standard error. ** P < .01 was considered significant

    Article Snippet: Serum IL‐34 levels were analyzed by ELISA assay (R&D Systems, Minneapolis, MN, USA).

    Techniques: CCK-8 Assay, Transfection, Infection, Plasmid Preparation

    IL‐34 inhibits apoptotic rates on PTC cells. Cell apoptosis was determined by flow cytometry after transfected with si‐IL‐34 or si‐NC in TPC‐1 (A) and K1 cells (B). Cell apoptosis in TPC‐1 (C) and K1 cells (D) which were infected with lenti‐vector or lenti‐IL‐34. The apoptotic rates were shown. Data were presented as the means ± standard error. ** P < .01 was considered significant

    Journal: Journal of Clinical Laboratory Analysis

    Article Title: IL‐34 is a potential biomarker for the treatment of papillary thyroid cancer

    doi: 10.1002/jcla.23335

    Figure Lengend Snippet: IL‐34 inhibits apoptotic rates on PTC cells. Cell apoptosis was determined by flow cytometry after transfected with si‐IL‐34 or si‐NC in TPC‐1 (A) and K1 cells (B). Cell apoptosis in TPC‐1 (C) and K1 cells (D) which were infected with lenti‐vector or lenti‐IL‐34. The apoptotic rates were shown. Data were presented as the means ± standard error. ** P < .01 was considered significant

    Article Snippet: Serum IL‐34 levels were analyzed by ELISA assay (R&D Systems, Minneapolis, MN, USA).

    Techniques: Flow Cytometry, Transfection, Infection, Plasmid Preparation

    IL‐34 promotes the invasion via on PTC cells. Two PTC cell lines were not only transfected with si‐IL‐34 or si‐NC were also infected with lenti‐vector or lenti‐IL‐34 for 48 h. A, The protein expression levels of E‐cadherin, N‐cadherin, and Vimentin were measured by Western blotting in PTC cells. The ratios of EMT biomarkers when transfected with si‐IL‐34 or si‐NC were determined to give a mean net density in TPC‐1 (B) and K1 cells (C). The ratios of EMT biomarkers when infected with lenti‐vector or lenti‐IL‐34 were determined to give a mean net density in TPC‐1 (D) and K1 cells (E). Data were presented as the means ± standard error. ** P < .01 was considered significant

    Journal: Journal of Clinical Laboratory Analysis

    Article Title: IL‐34 is a potential biomarker for the treatment of papillary thyroid cancer

    doi: 10.1002/jcla.23335

    Figure Lengend Snippet: IL‐34 promotes the invasion via on PTC cells. Two PTC cell lines were not only transfected with si‐IL‐34 or si‐NC were also infected with lenti‐vector or lenti‐IL‐34 for 48 h. A, The protein expression levels of E‐cadherin, N‐cadherin, and Vimentin were measured by Western blotting in PTC cells. The ratios of EMT biomarkers when transfected with si‐IL‐34 or si‐NC were determined to give a mean net density in TPC‐1 (B) and K1 cells (C). The ratios of EMT biomarkers when infected with lenti‐vector or lenti‐IL‐34 were determined to give a mean net density in TPC‐1 (D) and K1 cells (E). Data were presented as the means ± standard error. ** P < .01 was considered significant

    Article Snippet: Serum IL‐34 levels were analyzed by ELISA assay (R&D Systems, Minneapolis, MN, USA).

    Techniques: Transfection, Infection, Plasmid Preparation, Expressing, Western Blot

    IL‐34 promotes the invasion and activates the ERK signaling pathway on PTC cells. Two PTC cell lines were transfected with si‐IL‐34 or si‐NC were also infected with lenti‐vector or lenti‐IL‐34 for 48 h. A, The protein expression levels of p‐ERK and ERK were measured by Western blotting in PTC cells. The ratios of ERK and p‐ERK when transfected with si‐IL‐34 or si‐NC were determined to give a mean net density in TPC‐1 (B) and K1 cells (C). The ratios of ERK and p‐ERK when infected with lenti‐vector or lenti‐IL‐34 were determined to give a mean net density inTPC‐1 (D) and K1 cells (E). Data were presented as the means ± standard error. ** P < .01 was considered significant

    Journal: Journal of Clinical Laboratory Analysis

    Article Title: IL‐34 is a potential biomarker for the treatment of papillary thyroid cancer

    doi: 10.1002/jcla.23335

    Figure Lengend Snippet: IL‐34 promotes the invasion and activates the ERK signaling pathway on PTC cells. Two PTC cell lines were transfected with si‐IL‐34 or si‐NC were also infected with lenti‐vector or lenti‐IL‐34 for 48 h. A, The protein expression levels of p‐ERK and ERK were measured by Western blotting in PTC cells. The ratios of ERK and p‐ERK when transfected with si‐IL‐34 or si‐NC were determined to give a mean net density in TPC‐1 (B) and K1 cells (C). The ratios of ERK and p‐ERK when infected with lenti‐vector or lenti‐IL‐34 were determined to give a mean net density inTPC‐1 (D) and K1 cells (E). Data were presented as the means ± standard error. ** P < .01 was considered significant

    Article Snippet: Serum IL‐34 levels were analyzed by ELISA assay (R&D Systems, Minneapolis, MN, USA).

    Techniques: Transfection, Infection, Plasmid Preparation, Expressing, Western Blot