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Anti phospho p38 mitogen activated protein kinase

Manufactured by Cell Signaling Technology

Anti-phospho-p38 mitogen-activated protein kinase (MAPK) is a research-use-only lab reagent that can detect the phosphorylated form of p38 MAPK. p38 MAPK is a member of the MAPK family of proteins that play a key role in cellular stress response pathways.

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2 protocols using anti phospho p38 mitogen activated protein kinase

1

Investigating Inflammatory Signaling Pathways

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Recombinant human TNF-α was purchased from Peprotech and 2′,7′-dichlorofluorescein diacetate (DCF-DA) was purchased from Sigma–Aldrich. The following antibodies were used: anti-SOD3 for western blotting (ab83108) and anti-SOD3 for immunohistochemistry (IHC; ab171738) from Abcam; anti-glyceraldehyde dehydrogenase (GAPDH; ab83108) from AbClone; anti-phospho-NF-κB inhibitor protein ɑ (IκBɑ), anti-phospho-NF-κB p65, anti-phospho-c-jun N-terminal kinase (JNK), anti-JNK, anti-phospho-p38 mitogen-activated protein kinase (MAPK) (Cell Signaling Technology), anti-NF-κB p65, anti-p38 MAPK, anti-phospho-extracellular signal-regulated kinase (ERK), and anti-ERK2 from Santa Cruz Biotechnology; and anti-collagen type I cleavage site from ImmunoGlobe. Anti-MMP-1 and procollagen α1(I) N-propeptide (pN-ColIα1) antibodies have been previously described [21 (link)]. Horseradish peroxidase (HRP)-conjugated goat anti-mouse IgG and goat anti-rabbit IgG were purchased from KOMA Biotech (Seoul, Korea). Alexa Fluor® 488 goat anti-rabbit IgG (H+L) and rhodamine Red-X-conjugated goat anti-mouse IgG were purchased from Thermo Fisher Scientific (Waltham, MA, USA). SPlink HRP Detection Bulk Kit for Mouse and Rabbit Antibodies and Liquid AEC Substrate Kit (20×) for IHC were purchased from GBI labs (Bothell, WA, USA).
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2

NF-κB Signaling Pathway Analysis

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Aliquots containing 1 3 10 6 cells were washed with PBS and lysed in RIPA buffer (150 mmol/L NaCl, 1.0% NP-40, 0.1% SDS, 0.1% sodium deoxycholate, 5 mmol/L EDTA, and 10 mmol/L Tris-HCl, pH 7.4) containing protease inhibitors. Proteins were separated by using SDS-PAGE and transferred to membranes, and blots were probed with the following primary antibodies: anti-TNFAIP3, anti-phospho-IKKa/b Ser176/180, anti-IKKa, anti-phospho-IkBa Ser32, anti-IkBa, anti-phospho-NF-kB p65 Ser536, anti-NF-kB p65, anti-phospho-p38 mitogen-activated protein kinase (MAPK), anti-p38 MAPK, anti-SMC1 (all from Cell Signaling, Danvers, Mass), anti-glyceraldehyde-3-phosphate dehydrogenase, anti-CASP3 (GeneTex, Irvine, Calif), anti-green fluorescent protein (GFP; TaKaRa Clontech, Siga, Japan), or anti-b-actin (Sigma-Aldrich, St Louis, Mo). Primary antibodies were detected with horseradish peroxidase-conjugated anti-rabbit or anti-mouse secondary antibody (GE Healthcare, Little Chalfont, United Kingdom).
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