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epo elisa kits  (Elabscience Biotechnology)


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    Elabscience Biotechnology epo elisa kits
    Epo Elisa Kits, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+epo+elisa+kit/Human+EPO+(Erythropoietin)+ELISA+Kit/pm40446862-68-13-17
    Average 93 stars, based on 12 article reviews
    epo elisa kits - by Bioz Stars, 2026-11
    93/100 stars

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    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: Role of endothelial dysfunction in relation to prothrombogenesis in polycythemia vera
    Article Snippet: For all patients, and control group, CBC parameters were recorded, in addition, to report of JAK2 mutation for PV group (Quantitative PCR kit, Bioneer company/Korea). .. Serum Epo (Human EPO ELISA Kit, Elabscience, China), vWF (Human vWF ELISA Kit, Elabscience, China), and TM (Human TM ELISA Kit, Elabscience, China) were assessed for all patients. ..

    Article Title: Deficiency of lysophosphatidic acid receptor 3 decreases erythropoietin production in hypoxic mouse kidneys
    Article Snippet: An HRP-conjugated goat anti-mouse antibody (Cat No: ZB-2301, ZSGB-BIO, Beijing, China) or an HRP-conjugated goat anti-rabbit antibody (Cat No: ZB-2305, ZSGB-BIO, Beijing, China) was used as the secondary antibody to detect chemiluminescence signals (Cat No: WBKLS0500; Millipore, CA, USA). .. For the ELISA analysis of EPO protein in the supernatant of the culture medium, the Human EPO ELISA Kit (Cat No: E-EL-H3640; Elabscience, Wuhan, China) was used. ..

    Article Title: Effects of Hypoxemia by Acute High-Altitude Exposure on Human Intestinal Flora and Metabolism.
    Article Snippet: .. The Elabscience® Human EPO ELISA Kit (product number: E-EL-H3640c) from Elabscience Biotechnology Co., Ltd. (Houston, TX, USA) was used to measure serum EPO content. ..

    Article Title: Serum erythropoietin in acute ischemic stroke: preliminary findings
    Article Snippet: .. Serum EPO (pg/mL) was determined using a human EPO Elisa kit (E-EL-H3640, Elabscience, USA). ..



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    FIGURE 1 Evaluation of mRNA yield, capping efficiency, and potency of reporter genes using capping library screening. (a) SmartCap® (SC) library composition with ribose and base modification. In synthesized eGFP mRNA, (b) IVT products on 1% agarose gel, (c) capping efficiency of several 5′-cap analogues, (d) naked eGFP mRNA transfection-mediated fluorescence in HEK293T and Huh7 were evaluated. (e) In hEPO mRNA synthesis, mRNA yield, and potency were determined via hEPO <t>ELISA</t> assay in HEK293T and RD cell culture media. (f) In fLUC mRNA synthesis, yield, and potency were determined via luciferase assay in HEK293T and C2C12 cell lysate. (h) Female BALB/c mice were intramuscularly injected with PBS or a 5 mg dose of fLUC (Capping with SmartCap® library) mRNA LNPs. Luminescence was determined via IVIS (IVIS spectrum, PerkinElmer) up to 6 days p.i. Luminescence image from the whole body was measured over time for up to 6 days p.i. (h) Total flux of the whole body was plotted over time. Statistical analyses were performed using one-way ANOVA (*p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001, FF ns: no significant).
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    Image Search Results


    Impairment of hematopoietic function. a) Comparison of changes in CD34 + , b) Comparison of changes in CFU-GM, c) Comparison of changes in BFU-E, d) Comparison of changes in CXCL12, e) Comparison of changes in EPO, f) Comparison of changes in TPO. Note: 'a' indicates P < 0.05 compared with T0, 'b' indicates comparison with T1, and 'c' indicates P < 0.05 compared with the IV group at the same time.

    Journal: Journal of Medical Biochemistry

    Article Title: Randomized controlled trial of intraosseous access vs. intravenous access in traumatic hemorrhagic shock: Effects on inflammation, hematopoiesis, and coagulation

    doi: 10.5937/jomb0-58956

    Figure Lengend Snippet: Impairment of hematopoietic function. a) Comparison of changes in CD34 + , b) Comparison of changes in CFU-GM, c) Comparison of changes in BFU-E, d) Comparison of changes in CXCL12, e) Comparison of changes in EPO, f) Comparison of changes in TPO. Note: 'a' indicates P < 0.05 compared with T0, 'b' indicates comparison with T1, and 'c' indicates P < 0.05 compared with the IV group at the same time.

    Article Snippet: The following indicators were analyzed: IL-1β (DLB50), IL-6 (D6050B), IL-10 (D1000B), HMGB1 (IC1690G), CXCL12 (MAB310), EPO (DEPRU0), and TPO (BAF288): These markers were quantified using enzyme-linked immunosorbent assay (ELISA) with commercially available kits (R&D Systems).

    Techniques: Comparison

    FIGURE 1 Evaluation of mRNA yield, capping efficiency, and potency of reporter genes using capping library screening. (a) SmartCap® (SC) library composition with ribose and base modification. In synthesized eGFP mRNA, (b) IVT products on 1% agarose gel, (c) capping efficiency of several 5′-cap analogues, (d) naked eGFP mRNA transfection-mediated fluorescence in HEK293T and Huh7 were evaluated. (e) In hEPO mRNA synthesis, mRNA yield, and potency were determined via hEPO ELISA assay in HEK293T and RD cell culture media. (f) In fLUC mRNA synthesis, yield, and potency were determined via luciferase assay in HEK293T and C2C12 cell lysate. (h) Female BALB/c mice were intramuscularly injected with PBS or a 5 mg dose of fLUC (Capping with SmartCap® library) mRNA LNPs. Luminescence was determined via IVIS (IVIS spectrum, PerkinElmer) up to 6 days p.i. Luminescence image from the whole body was measured over time for up to 6 days p.i. (h) Total flux of the whole body was plotted over time. Statistical analyses were performed using one-way ANOVA (*p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001, FF ns: no significant).

    Journal: Frontiers in immunology

    Article Title: Discovery and development of a safe and efficient COVID-19 mRNA vaccine, STP2104, using a novel capping library screening method.

    doi: 10.3389/fimmu.2025.1571713

    Figure Lengend Snippet: FIGURE 1 Evaluation of mRNA yield, capping efficiency, and potency of reporter genes using capping library screening. (a) SmartCap® (SC) library composition with ribose and base modification. In synthesized eGFP mRNA, (b) IVT products on 1% agarose gel, (c) capping efficiency of several 5′-cap analogues, (d) naked eGFP mRNA transfection-mediated fluorescence in HEK293T and Huh7 were evaluated. (e) In hEPO mRNA synthesis, mRNA yield, and potency were determined via hEPO ELISA assay in HEK293T and RD cell culture media. (f) In fLUC mRNA synthesis, yield, and potency were determined via luciferase assay in HEK293T and C2C12 cell lysate. (h) Female BALB/c mice were intramuscularly injected with PBS or a 5 mg dose of fLUC (Capping with SmartCap® library) mRNA LNPs. Luminescence was determined via IVIS (IVIS spectrum, PerkinElmer) up to 6 days p.i. Luminescence image from the whole body was measured over time for up to 6 days p.i. (h) Total flux of the whole body was plotted over time. Statistical analyses were performed using one-way ANOVA (*p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001, FF ns: no significant).

    Article Snippet: For mRNA transfection, HEK293T cells (1 × 106 cells/well) were plated in 6-well plates and cultured in GibcoTM Opti-MEMTM Reduced Serum Medium (Thermo Fisher Scientific) for 24 h. After 24 h of transfection, the fluorescence expressed by eGFP and hEPO in the cell cultures was analyzed by using an EVOS M5000 Microscope (Thermo Fisher Scientific) with a 10X scope and a Human Erythropoietin/EPO ELISA Kit (BioTechne® R&D System, Quantikine DEPRU0, Minneapolis, MN, USA), respectively.

    Techniques: Library Screening, Synthesized, Agarose Gel Electrophoresis, Analogues, Transfection, Enzyme-linked Immunosorbent Assay, Cell Culture, Luciferase, Injection