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Polyvinylidene difluoride pvdf membrane

Manufactured by Merck Group
Sourced in United States, Germany, China, United Kingdom, Morocco, Ireland, Japan, France, Spain, Belgium, Italy
About the product

Polyvinylidene difluoride (PVDF) membranes are a type of lab equipment used for various applications. PVDF membranes are known for their chemical and thermal resistance, making them suitable for a range of laboratory procedures. They are commonly used in techniques such as Western blotting, protein and nucleic acid detection, and sample preparation. The core function of PVDF membranes is to serve as a support and transfer medium for biomolecules in analytical and preparative processes.

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Market Availability & Pricing

The Immobilon®-P Polyvinylidene Difluoride (PVDF) membrane is commercially available from Merck Group and its authorized distributors. This membrane is commonly used in Western blotting for protein transfer after SDS-PAGE.

Prices for the Immobilon®-P PVDF membrane vary depending on size and quantity. For fluorescent detection applications, Merck offers the Immobilon®-FL PVDF membrane, which features low background fluorescence and is compatible with visible and infrared fluorescent probes.

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1 008 protocols using «polyvinylidene difluoride pvdf membrane»

1

Epigenetic Regulation in Cell Cultures

2025
RPMI-1640 and DMEM high glucose culture media, Fetal Bovine Serum (FBS), Phosphate Buffer Saline (PBS), L-glutamine and penicillin/streptomycin were purchased from Biosera (Kansas, MO, USA). Zebularine and SYBR green qPCR master mix (high rox) were purchased from MedChem (Stockholm, Sweden). SFN and IBN were purchased from Abcam (Cambridge, UK), while BITC was purchased from Sigma-Aldrich (St. Louis, MO, USA). Resazurin sodium salt was purchased from Fluorochem (Hadfield, UK). Caspases-3, -8 and -9 multiplex activity assay kit was obtained from Abcam (Cambridge, UK). PrimeScript RT reagent kit was purchased from TaKaRa (Shiga, Japan) and NucleoZOL from Macherey-Nagel (Duren, Germany). Primers were purchased from Invitrogen (Waltham, MA, USA). Polyvinylidene difluoride (PVDF) membranes were purchased from Millipore (Bedford, MA, USA), whereas chemiluminescence reagents, proteinase, phosphatase inhibitors and the Pierce™ BCA protein assay kit were purchased from Thermo Scientific (Rockford, IL, USA). All antibodies (anti-DNMT1, anti-DNMT3A, anti-DNMT3B, anti-H3K4me2, anti-H3K4me3, anti-H3K9me2, anti-H3K9me3 and anti-H3K9ac) were obtained from Cell Signaling Technology (Boston, MA, USA), while anti-β actin was purchased from Sigma-Aldrich (Taufkirchen, Germany). Secondary horseradish peroxidase conjugated antibodies were purchased from Millipore (Bedford, MA, USA). Finally, glutaraldehyde (25%), osmium tetroxide, propylene oxide, araldite resin, agar 100 resin, dodenyl succinic anhydride (DDSA), 2,4,6-Tri(dimethylaminomethyl) phenol (DMP-30), uranyl acetate and lead citrate were all purchased from Agar Scientific (Essex, UK).
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2

Protein Expression Analysis Using Western Blot

2025
Proteins were extracted using the radioimmunoprecipitation assay (KGI Biologicals, Inc, Jiangsu, China). The total protein concentrations were measured using the bicinchoninic acid (BCA) protein assay kit (KGI Biologicals, Inc, Jiangsu, China). In brief, 25 μg of proteins were loaded into each lane of sodium dodecyl sulfate polyacrylamide gels, separated by 8% sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) gels and transferred onto the polyvinylidene difluoride (PVDF) membrane (Millipore, USA). After blocking with 5% fat-free milk for 2 h, the PVDF membranes were incubated with the following primary antibodies: Anti-MGL antibody (1:1,000) (cat. no. GR3397231-1; Abcam, UK), anti-TLR4 antibody (1:1,000) (cat. no. sc-293072GR3397231-1; Santa Cruz, USA), anti-Erk1/2 antibody (1:1,000) (cat. no. ab4695S; Cell Signaling Technology, USA), anti-phospho-Erk1/2 antibody (1:1,000) (cat. no. 4376S; Cell Signaling Technology, USA), anti-P38 antibody (1:1,000) (cat. no. 8690S; Cell Signaling Technology, USA), anti-phospho-P38 antibody (1:1,000) (cat. no. 4092S; Cell Signaling Technology, USA), anti-JNK antibody (1:1,000) (cat. no. 9252S; Cell Signaling Technology, USA), anti-phospho-JNK antibody (1:1,000) (cat.no.4668S; Cell Signaling Technology, USA), anti-NF-κB antibody (1:1,000) (cat. no. 8242S; Cell Signaling Technology, USA), and anti-phospho NF-κB antibody (1:1,000) (cat. no. 3033S; Cell Signaling Technology, USA). After three washes with tris-buffered saline containing Tween® 20 (TBST), the PVDF membranes were incubated with secondary antibodies GAPDH peroxidase-linked Ab (ZSGB-BIO Technology Co., Ltd., Beijing, China; 1:5000) at room temperature (about 25°C) for 1 h. The gray value of protein bands, utilized to assess protein expression levels, was analyzed using Image-Pro Plus software.
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3

Mitochondrial Purity Assessment by Western Blot

2025
In order to check the purity of the isolated mitochondrial fraction, western blot was performed by using mitochondrial (anti‐translocase of outer membrane 20 (TOM20)), cytoplasmic (anti‐ß‐tubulin), and nuclear (anti‐Histone H3) markers. The total extracted protein was quantified using the Pierce Bicinchoninic Acid (BCA) Protein Assay Kit (Thermo Scientific) and 30 μg of proteins were loaded into a 15% sodium dodecyl sulphate (SDS) containing polyacrylamide gel electrophoresis (PAGE) and transferred onto a polyvinylidene difluoride (PVDF) membrane (Millipore). Subsequently, the membrane was subjected to blocking for 1 h at room temperature, then incubated with a primary antibody overnight at 4°C, followed by a horse radish peroxidase (HRP)‐conjugated secondary antibody for 1 h at room temperature. Antibodies and dilutions utilised for western blot are as follows: TOM20 (Cell Signaling, 42,406) (1:1000), Histone H3 (Cell Signaling, 9715) (1:1000), ß‐tubulin (Sigma, T5201) (1:3000), HRP‐conjugated goat anti‐rabbit IgG (H + L) (Invitrogen) (1:5000), and HRP‐conjugated goat anti‐mouse IgG (H + L) (Invitrogen) (15000). Protein bands were visualised using the Super Signal West Femto Maximum Sensitivity Substrate (Thermo Scientific) via the GeneGnome5 Chemiluminescence imaging system (Syngene). The band intensities were quantitatively analysed using ImageJ (version 2.9.0/1.54f, NIH).
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4

Macrophage Polarization and Extracellular Vesicle Regulation

2025
The human bronchial epithelial (BEAS-2B) cell line and human monocyte (THP-1) cell line were acquired from The Cell Bank of Type Culture Collection of The Chinese Academy of Sciences (Beijing, China). Dulbecco’s modified Eagle’s medium (DMEM), Roswell Park Memorial Institute (RPMI) 1640, and fetal bovine serum (FBS) were procured from Thermo Fisher Scientific, Inc. (Massachusetts, USA). Phorbol-12-myristate-13-acetate (PMA, cat. no. S1819) was obtained from Beyotime Biotechnology (Jiangsu, China), and IL-4 (cat. no. M9363) was obtained from Abmole Biotechnology LTD. (Texas, USA). CD68 (cat. no. 12-0689-41), CD80 (cat. no. 11-0809-41), and CD206 (cat. no. 17-2069-41) were acquired from Thermo Fisher Scientific, Inc. The PKH67 Green Fluorescent Cell Linker Kit and 4′,6-diamidino-2-phenylindole (DAPI) were acquired from Sigma‒Aldrich (Missouri, USA), while phosphotungstic acid hydrate was purchased from Beijing Solarbio Science & Technology Co., Ltd. (Beijing, China). SB431542 and GW4869 were acquired from MedChemExpress, LLC. (Shanghai, China). A BCA protein quantification kit was obtained from CoWin Biosciences (Jiangsu, China), whereas polyvinylidene difluoride (PVDF) membranes were acquired from MilliporeSigma (Massachusetts, USA). Exosome-depleted FBS (Exo-FBS, cat. no. EXO-FBS-250A-1) was purchased from System Biosciences, LLC. (California, USA). The primary antibodies against Smad3 (cat. no. ab40854), phosphorylated (p)‑Smad3 (cat. no. ab52903), and Smad7 (cat. no. ab216428) were obtained from Abcam (Cambridge, United Kingdom). Anti-snail (cat. no. 3879), anti-p-Smad2 (cat. no. AP0269), anti-CD81 (cat. no. GB111073), anti-TSG101 (cat. no. GB15618), anti-Vimentin (cat. no. GB11192), anti-Collagen 1 (cat. no. GB114197), anti-E-cadherin (cat. no. GB11868), anti-TGF-βRI (cat. no. GB11271), anti-Smad2 (cat. no. GB11511), anti-GAPDH (cat. no. GB11002) and an HRP‑conjugated goat anti‑rabbit IgG secondary antibody (cat. no. GB23303) were purchased from Cell Signaling Technology, Inc. (Massachusetts, USA), ABclonal, Inc. (Massachusetts, USA), and Wuhan Servicebio Technology Co., Ltd. (Hubei, China), respectively.
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5

Hematoporphyrin Derivatives Photodynamic Therapy

2025
RPMI-1640 medium, fetal bovine serum, trypsin, and dual, antibodies (100 U/ml penicillin and 0.1 mg/ml streptomycin), were purchased from Hyclone (USA); dimethyl, sulfoxide (DMSO) was a product of Sigma, (USA). The UV-visible spectra of HPD were recorded in dimethyl sulfoxide (DMSO), the solvent used for HPD preparation. The absorption peaks of HPD were observed at 405 nm (Soret band) and 630 nm (Q-band) (showing in supplementary Figure S1). Hematoxylin-eosin (HE) staining kit and TdT-mediated dUTP nick end labeling (TUNEL) apoptosis detection kit were purchased from Roche (Switzerland); RIPA lysis buffer and BCA (acid) protein assay kit were purchased from Solarbio (China); reverse transcription kit and SYBR Green quantitative PCR kit were purchased from Solarbio (China). TaKaRa (Japan); Western blotting primary and secondary antibody dilutions were purchased from BOSTER Bio (Wuhan, China); polyvinylidene difluoride (PVDF) membranes and ECL chemiluminescence kits were obtained from MILLIPORE (USA); rabbit anti-mouse Caspase-3, rabbit anti-mouse Survivin, rabbit anti-mouse Bax, hematoporphyrin derivatives (10 mM × 1 ml in dimethyl sulfoxide), were purchased from Beijing Solarbio Company (China), and were shipped in batches and stored in a refrigerator at 4 °C under dark conditions. HPD was determined using RPMI-1640 medium. The LED-IB photodynamic therapy instrument used in the experiment was made by Wuhan Yage. It can output 630 nm of red light with an output power density of 80mW/cm2 and works in continuous mode.
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