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Multi species tgf β elisa kit

Manufactured by Thermo Fisher Scientific
Sourced in United States

The Multi-species TGF-β ELISA kit is a quantitative sandwich enzyme-linked immunosorbent assay (ELISA) designed for the measurement of transforming growth factor beta (TGF-β) in various species samples. The kit utilizes a specific antibody coated on a microplate to capture the target analyte from the sample, and a detection antibody conjugated with an enzyme for colorimetric quantification. The assay provides a reliable and reproducible method for the quantitative detection of TGF-β levels in the sample.

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2 protocols using multi species tgf β elisa kit

1

Cytokine Profile in Cirrhotic Patients Pre- and Post-PPI

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Peripheral blood samples (3-4 mL) from 17 cirrhotic patients were drawn before and after treatment with PPIs. Blood samples were centrifuged and the sera were collected and stored aliquoted at -80°C until further use. The serum levels of cytokines IL-1β, -6, -8, -10, -12p70 and TNF-α were determined by a cytometric bead array method, using the Human Inflammatory Cytokine CBA kit (BD Bioscience, San Diego, USA). The measurements were performed on a BD FACS Array Bioanalyzer. The raw data were analyzed using the Flow Jo V7.5 software (Tree Star Inc., Ashland, OR, USA). Further analysis of the data was performed using the Curve Expert 1.4 software. Serum levels of TGF-β and LBP were determined by ELISA, using a multi-species TGF-β ELISA kit (Invitrogen Corporation, CA, USA) and a human LBP ELISA kit (SunRed Biological Technology, Shanghai). NOx levels were measured by a nitric oxide quantitation kit (Active Motif, Belgium). Endotoxin levels were measured using a LAL Chromogenic Endpoint assay (Hycult biotech, The Netherlands). Data analysis was performed using the Curve Expert 1.4 software. The detection limits of the methods employed were: IL-8=3.6 pg/mL, IL-1β=7.2 pg/mL, IL-6=2.5 pg/mL, IL-10=3.3 pg/mL, TNF-α=3.7 pg/mL, IL-12p70=1.9 pg/mL, LBP=0.135 μg/mL, TGF-β=15.6 pg/mL, NOx <1 μM, endotoxin=0.04 EU/mL.
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2

Cytokine Profiling in Biological Samples

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Serum levels of cytokines IL-1β, IL-6, IL-8, IL-10, IL-12p70, and TNF-α were determined by a cytometric bead array (CBA) method using the Human Inflammatory Cytokine CBA kit (BD Bioscience, San Diego, USA) as described (18 (link)). Measurements were performed using a BD FACS Array Bioanalyzer as described (18 (link)). Raw data were analyzed using Flow Jo V7.5 software (Tree Star Inc., Ashland, OR, USA). Serum TGF-β and LBP concentrations were determined using a multispecies TGF-β ELISA kit (Invitrogen Corporation, CA, USA) and a human LBP ELISA kit (SunRed Biological Technology, Shanghai) respectively, as described in (18 (link)). NO levels were measured using a nitric oxide quantification kit (Active Motif, Belgium), as described in (18 (link)). Endotoxin levels were measured using the Limulus amebocyte lysate chromogenic endpoint assay (Hycult Biotech, The Netherlands), as described in (18 (link)). Data analysis was performed using Curve Expert 1.4 software. The detection limits of the methods used were: IL-1β = 7.2 pg/ml, IL-8 = 3.6 pg/ml, IL-10 = 3.3 pg/ml, IL-6 = 2.5 pg/ml, IL12p70 = 1.9 pg/ml, TNF-α = 3.7 pg/ml, TGF-β = 15.6 pg/ml, LBP = 0.135 μg/ml, NO < 1 μM, endotoxin = 0.04 EU/ml.
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