The largest database of trusted experimental protocols

Polyethyleneimine pei

Manufactured by Fujifilm
Sourced in United States, Japan

Polyethyleneimine (PEI) is a versatile polymer that can be used in various laboratory applications. It is a water-soluble, cationic polymer with a high charge density, making it useful for applications such as nucleic acid or protein purification, cell transfection, and as a coating agent. PEI is available in different molecular weights and configurations to meet the specific requirements of different laboratory protocols.

Automatically generated - may contain errors

4 protocols using polyethyleneimine pei

1

Synthesis and Characterization of Gold Nanoparticles

Check if the same lab product or an alternative is used in the 5 most similar protocols
In this study, Milli-Q water (18.2 MΩ) was used to prepare all aqueous solutions. Chloroauric(III) acid tetrahydrate (HAuCl4, Nacalai Tesque, Kyoto, Japan), trisodium citrate dihydrate (Kanto Chemical, Tokyo, Japan), hydrochloric acid (Kishida Chemical, Osaka, Japan), silver nitrate (Fujifilm Wako Pure Chemical, Osaka, Japan), L-ascorbic acid (Tokyo Chemical Industry, Tokyo, Japan), 1-butanol (BuOH, Kishida Chemical), ethanol (Kishida Chemical), sodium hydroxide (Kanto Chemical), 16-mercaptohexadecanoic acid (MHA, Sigma–Aldrich, St. Louis, MO, USA), polyethyleneimine (PEI, MW: ~10,000, Fujifilm Wako Pure Chemical) and PVP (MW: ~55,000, Sigma–Aldrich, Saint Louis, MO, USA) were used without further purification.
+ Open protocol
+ Expand
2

Isolation and Differentiation of Rat eNSCs

Check if the same lab product or an alternative is used in the 5 most similar protocols
All eNSCs were obtained from telencephalon tissues of E14 Wistar Wt and Tg [Wistar-esTgN(Sox2/CD63-GFP)3NCCRI] rats. Isolated eNSCs were cultured on noncoated tissue culture plastic as neurospheres in KBM neural stem cell proliferation medium (Kohjin Bio, Saitama, Japan) with 0.2% KBM supplement containing EGF and bFGF (Kohjin Bio) at 37°C in air enriched with 5% CO2, as described previously (Yoshimura et al., 2016a (link)). After 3 or 4 days, neurospheres were dissociated using trypsin (Sigma-Aldrich) and passaged. Differentiation was carried out by seeding on tissue culture dishes pre-coated with 0.2% polyethyleneimine (PEI) (Wako). Differentiation medium consisted of KBM containing 2% B-27 serum-free supplement containing vitamin A (Life Technologies) without EGF and bFGF. Dissociated cells were plated at a density of 1.8×106 cells per 35 mm culture dish (Becton Dickinson). For immunocytochemistry, 1.4×105 cells/0.2 ml were reseeded on pre-coated glass-bottomed dishes (Matsunami, Osaka, Japan). The culture medium was changed 3 or 4 days after plating, and differentiation proceeded for 7 days. To promote the proliferation of differentiated astroglial cells, culture medium was replaced with astroglial culture medium (described in the next section) at 6 days after differentiation.
+ Open protocol
+ Expand
3

Preparation of PDA Particles and Emulsions

Check if the same lab product or an alternative is used in the 5 most similar protocols
Reagents used to prepare PDA particles were dopamine hydrochloride (DA–HCl, Kanto Chemical, Tokyo, Japan), tris(hydroxymethyl)aminomethane (Tris, Kanto Chemical), and methanol (Kanto Chemical). Oils used to prepare emulsions were n-dodecane (≥99%, Sigma-Aldrich, Tokyo, Japan), toluene (99%, Sigma-Aldrich), dichloromethane (DCM, ≥99.0%, Sigma-Aldrich), methyl myristate (95.0%, Wako Pure Chemical, Osaka, Japan), octafluorotoluene (97%, Wako Pure Chemical) and perfluorononane (99%, Wako Pure Chemical). Poly(ethylene imine) (PEI, Average Molecular Weight, approximately 600, Wako Pure Chemical) was used as a crosslinking agent for PDA particles. Poly(vinyl alcohol) (PVA) were purchased from Sigma-Aldrich. Deionized water (<0.06 µS·cm−1, Advantec MFS RFD240NA: GA25A-0715) was used for preparation of PDA particles and emulsions. All other chemicals and solvents were of reagent grade and used as received.
+ Open protocol
+ Expand
4

Enzymatic Alcohol Oxidation Assay

Check if the same lab product or an alternative is used in the 5 most similar protocols
Alcohol oxidase (AOD, A2404-1KU, from Pichia pastoris) was obtained from Sigma-Aldrich Japan (Tokyo, Japan). Formaldehyde dehydrogenase (FALDH, from Pseudomonas sp.) was from two different manufacturers, Funakoshi (Tokyo, Japan) and Toyobo (Osaka, Japan). An oxidized form of β-nicotinamide adenine dinucleotide (NAD+) was purchased from Oriental Yeast (Tokyo, Japan). A hydrophilic polytetrafluoroethylene (H-PTFE) membrane (thickness: 80 μm, porosity: 80%, pore size: 0.2 μm) was from Millipore (Burlington, MA, USA). Poly [2-methacryloyloxyethyl phosphorylcholine (MPC)-co-2-ethylhexyl methacrylate (EHMA)] (PMEH) was synthesized in house by the free radical-polymerization method [42 (link)]. Polyethyleneimine (PEI, average molecular weight of 10,000, 164-17821) and glutaraldehyde (GA, 079-00533) were purchased from Fujifilm Wako Pure Chemical (Osaka, Japan).
All reagents for the following buffer solutions were obtained from Fujifilm Wako Pure Chemical (Osaka, Japan). For the phosphate buffer (PB, 100 mM) solution, we added potassium dihydrogen phosphate solution (100 mM in ultrapure water) to disodium hydrogen phosphate solution (100 mM in ultrapure water) to buffer the solution pH from 6.5 to 8.5. For the Tris-HCl solution (100 mM), we added HCl solution to 100 mM trimethylolaminomethane solution to buffer the pH from 8.5 to 10.5.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!