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Tgf β1

Manufactured by Sangon
Sourced in China

TGF-β1 is a recombinant human transforming growth factor beta 1 protein. It is a member of the transforming growth factor beta superfamily of cytokines, which play important roles in cellular processes such as cell growth, cell differentiation, and immune regulation.

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4 protocols using tgf β1

1

Quantifying Cytokine Levels in Rat Serum

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Blood was drawn from about 1-cm capillaries under the eyelids, and serum was obtained after centrifuging at 3000 rpm for 5 min. IL-1β (MitcSciences, USA), TNF-α (Sangon Biotech, Shanghai, China), IL-10 (Sangon Biotech, Shanghai, China), and IL-17 (Sangon Biotech, Shanghai, China) ELISA kit for rats were used to detect the IL-1β, TNF-α, TGF-β1, and IL-17 levels, respectively, in serum.
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2

Evaluating Antioxidant and Renal Effects of Ginsenoside Rg1 and Astragaloside IV

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Ginsenoside Rg1 (purity ≥98%) and Astragaloside IV (purity ≥98%) were purchased from ChengDu ConBon Bio-tech Co., Ltd. (Chengdu, China). The methane dicarboxylic aldehyde (MDA), catalase (CAT), glutathione peroxidase (GSH-PX) and total anti-oxidative capacity (T-AOC) assay kits for rats were bought from Jiancheng Bioengineering Institute (Nanjing, China). Rat blood urea nitrogen (BUN), serum creatinine (SCr), β2-microglobulin (β2-MG) and urinary creatinine (UCr) ELISA kits were also purchased from Jiancheng Bioengineering Institute. Streptozotocin (STZ) was bought from Sigma (St Louis, MO, USA). Polyclonal antibodies used for immunohistochemical analysis included TGF-β1 (Santa Cruz Biotechnology, Dallas, TX, USA), Smad2/3 (Cell Sig-naling, Danvers, MA, China), Smad7 (Bioss, Woburn, MA, USA) and CTGF (Bioss). Rat SP immunohistochemistry kits were purchased from Thermo Fisher Scientific (Waltham, MA, USA). The primer sequences of TGF-β1, Smad7, CTGF and ACTB (listed in Table 1) used for real-time PCR analysis were bought from Sangon Biotech Co., Ltd (Shanghai, China). Real-Time PCR Reagents & Kits and Total RNA Extractor (Trizol) were bought from Thermo Fisher Scientific. The other reagents used were of analytical grade.
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3

Cutaneous Gene Expression Profiling

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The cutaneous and cellular RNA was extracted and underwent qRT-PCR analysis for determining the RNA levels, using primers for actin alpha 2 (Actα2), angiopoietin-2 (Angpt2), angiopoietin-4 (Angpt4), collagen type I alpha 1 (Col1α1), E-CADHERIN, fibronectin (Fn), Interleukin-10 (Il-10), interleukin 1 beta (Il-1β), matrix metalloproteinase1 (Mmp1), matrix metalloproteinase 1 (Mmp2), nitric oxide synthase 2 (Nos2), Rplp0, Serpine1, Tgf-β1, vascular cell adhesion molecule 1 (Vcam1), and vascular endothelial growth factor (VEGF-A, Sangon Biotech, Shanghai, China). The procedures for RNA extraction and qRT-PCR were described previously [12 (link)]. The sequences of the primers are provided in Table S3.
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4

Overexpression of NCK1-AS1 and TGF-β1 in Prostate Cancer

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NCK1-AS1 and TGF-β1 expression vectors were constructed by Sangon Biotech Co., Ltd. using a pcDNA3 vector. DU145 and 22Rv1 cells were collected when they had reached 70–90% confluence. Lipofectamine® 2000 reagent (Thermo Fisher Scientific, Inc.) was used transfect 10 nM NCK1-AS1 or TGF-β1 expression vector, or 10 nM empty vector (negative control group; NC) into 105 DU145 or 22Rv1 cells. This experiment also included cells that had not undergone transfection to serve as control cells (Control group; C). All subsequent experiments were performed using cells collected at 24 h after transfection.
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