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human lambda light chain  (Bethyl)


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    Structured Review

    Bethyl human lambda light chain
    Human Lambda Light Chain, supplied by Bethyl, used in various techniques. Bioz Stars score: 93/100, based on 52 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human lambda light chain/product/Bethyl
    Average 93 stars, based on 52 article reviews
    human lambda light chain - by Bioz Stars, 2026-03
    93/100 stars

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    Bethyl lambda light chain elisa human lambda light chain kit
    RPMI-8226 cells were incubated for 48 hours in the presence or absence of lovastatin (Lov, 10 μM) or varying concentrations of the test compounds. A) Intracellular <t>lambda</t> light chain concentrations were determined via <t>ELISA.</t> Data are expressed as a percentage of control (mean + SD, n=3). The * denotes p < 0.05 per unpaired two-tailed t-test. B) Immunoblot analysis of Rap1a (antibody detects only unmodified protein) and β-tubulin (as a loading control).
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    RPMI-8226 cells were incubated for 48 hours in the presence or absence of lovastatin (Lov, 10 μM) or varying concentrations of the test compounds. A) Intracellular lambda light chain concentrations were determined via ELISA. Data are expressed as a percentage of control (mean + SD, n=3). The * denotes p < 0.05 per unpaired two-tailed t-test. B) Immunoblot analysis of Rap1a (antibody detects only unmodified protein) and β-tubulin (as a loading control).

    Journal: Bioorganic & medicinal chemistry

    Article Title: α-Methylation Enhances the Potency of Isoprenoid Triazole Bisphosphonates as Geranylgeranyl Diphosphate Synthase Inhibitors

    doi: 10.1016/j.bmc.2017.10.023

    Figure Lengend Snippet: RPMI-8226 cells were incubated for 48 hours in the presence or absence of lovastatin (Lov, 10 μM) or varying concentrations of the test compounds. A) Intracellular lambda light chain concentrations were determined via ELISA. Data are expressed as a percentage of control (mean + SD, n=3). The * denotes p < 0.05 per unpaired two-tailed t-test. B) Immunoblot analysis of Rap1a (antibody detects only unmodified protein) and β-tubulin (as a loading control).

    Article Snippet: 5.23 Lambda light chain ELISA Human lambda light chain kit (Bethyl Laboratories, Montgomery, TX) was used to quantify intracellular monoclonal protein levels of whole cell lysate.

    Techniques: Incubation, Enzyme-linked Immunosorbent Assay, Control, Two Tailed Test, Western Blot

    RPMI-8226 cells were incubated for 48 hours in the presence or absence of lovastatin (Lov, 10 μM) or varying concentrations of the test compound. A) Intracellular lambda light chain concentrations were determined via ELISA. Data are expressed as a percentage of control (mean + SD, n=3). The * denotes p < 0.05 per unpaired two-tailed t-test. B) Immunoblot analysis of Rap1a (antibody detects only unmodified protein) and β-tubulin (as a loading control).

    Journal: Bioorganic & medicinal chemistry

    Article Title: α-Methylation Enhances the Potency of Isoprenoid Triazole Bisphosphonates as Geranylgeranyl Diphosphate Synthase Inhibitors

    doi: 10.1016/j.bmc.2017.10.023

    Figure Lengend Snippet: RPMI-8226 cells were incubated for 48 hours in the presence or absence of lovastatin (Lov, 10 μM) or varying concentrations of the test compound. A) Intracellular lambda light chain concentrations were determined via ELISA. Data are expressed as a percentage of control (mean + SD, n=3). The * denotes p < 0.05 per unpaired two-tailed t-test. B) Immunoblot analysis of Rap1a (antibody detects only unmodified protein) and β-tubulin (as a loading control).

    Article Snippet: 5.23 Lambda light chain ELISA Human lambda light chain kit (Bethyl Laboratories, Montgomery, TX) was used to quantify intracellular monoclonal protein levels of whole cell lysate.

    Techniques: Incubation, Enzyme-linked Immunosorbent Assay, Control, Two Tailed Test, Western Blot

    RPMI-8226 cells were incubated for 48 hours in the presence or absence of lovastatin (Lov, 10 μM) or varying concentrations of the test compounds. A) Intracellular lambda light chain concentrations were determined via ELISA. Data are expressed as a percentage of control (mean + SD, n=3). The * denotes p < 0.05 per unpaired two-tailed t-test. B) Immunoblot analysis of Rap1a (antibody detects only unmodified protein) and β-tubulin (as a loading control).

    Journal: Bioorganic & medicinal chemistry

    Article Title: α-Methylation Enhances the Potency of Isoprenoid Triazole Bisphosphonates as Geranylgeranyl Diphosphate Synthase Inhibitors

    doi: 10.1016/j.bmc.2017.10.023

    Figure Lengend Snippet: RPMI-8226 cells were incubated for 48 hours in the presence or absence of lovastatin (Lov, 10 μM) or varying concentrations of the test compounds. A) Intracellular lambda light chain concentrations were determined via ELISA. Data are expressed as a percentage of control (mean + SD, n=3). The * denotes p < 0.05 per unpaired two-tailed t-test. B) Immunoblot analysis of Rap1a (antibody detects only unmodified protein) and β-tubulin (as a loading control).

    Article Snippet: 5.23 Lambda light chain ELISA Human lambda light chain kit (Bethyl Laboratories, Montgomery, TX) was used to quantify intracellular monoclonal protein levels of whole cell lysate.

    Techniques: Incubation, Enzyme-linked Immunosorbent Assay, Control, Two Tailed Test, Western Blot

    RPMI-8226 cells were incubated for 48 hours in the presence or absence of lovastatin (Lov, 10 μM) or varying concentrations of the test compounds. A) Intracellular lambda light chain concentrations were determined via ELISA. Data are expressed as a percentage of control (mean + SD, n=3). The * denotes p < 0.05 per unpaired two-tailed t-test. B) Immunoblot analysis of Rap1a (antibody detects only unmodified protein) and β-tubulin (as a loading control).

    Journal: Bioorganic & medicinal chemistry

    Article Title: α-Methylation Enhances the Potency of Isoprenoid Triazole Bisphosphonates as Geranylgeranyl Diphosphate Synthase Inhibitors

    doi: 10.1016/j.bmc.2017.10.023

    Figure Lengend Snippet: RPMI-8226 cells were incubated for 48 hours in the presence or absence of lovastatin (Lov, 10 μM) or varying concentrations of the test compounds. A) Intracellular lambda light chain concentrations were determined via ELISA. Data are expressed as a percentage of control (mean + SD, n=3). The * denotes p < 0.05 per unpaired two-tailed t-test. B) Immunoblot analysis of Rap1a (antibody detects only unmodified protein) and β-tubulin (as a loading control).

    Article Snippet: 5.23 Lambda light chain ELISA Human lambda light chain kit (Bethyl Laboratories, Montgomery, TX) was used to quantify intracellular monoclonal protein levels of whole cell lysate.

    Techniques: Incubation, Enzyme-linked Immunosorbent Assay, Control, Two Tailed Test, Western Blot