The largest database of trusted experimental protocols

2 protocols using 1 ethyl 3 3 dimethylaminopropyl carbodiimide

1

Comprehensive Analytical Reagent Procurement

Check if the same lab product or an alternative is used in the 5 most similar protocols
Acetone, diethylether, magnesium sulfate, sodium hydroxide, dichloromethane, chlorobenzene, toluene, ethyl acetate, methanol, ethylbenzene, butylbenzene, hexylbenzene, phenyloctane, tetrahydrofuran (THF), chloroform, n-hexane were purchased from Nacalai Tesque (Kyoto, Japan), methyl pentafluorobenzoate (MPFB), diethyl amine, 3-aminopropyltrimethoxysilane (APTMS), d-( +)-trehalose dihydrate from Tokyo Chemical Industry (Tokyo, Japan), sodium azide, N-hydroxysuccinimide (NHS), 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDAC), d-( +)-glucose, maltose monohydrate, sucrose from Wako Pure Chemical Industries (Osaka, Japan), C60-fullerene (C60), C70-fullerene (C70), dextran (Mw = 1,000) (glucose homopolymer) from Sigma-Aldrich Japan (Tokyo, Japan), 2-AB Dextran Calibration Ladder (2-AB labeled glucose homopolymer) from Waters (USA), respectively. Deionized water was obtained by a Milli-Q Direct-Q 3UV system (Merck Millipore, Tokyo, Japan). Silica monolithic capillaries (ULTRON HF-SIL, ULTRON HF-ODS) were purchased from Shinwa Chemical Industries Ltd. (Kyoto, Japan). Porous graphite carbon column (PGC column) was purchased from Thermo Fischer Scientific USA).
+ Open protocol
+ Expand
2

Gelatin Sponge Preparation and Functionalization

Check if the same lab product or an alternative is used in the 5 most similar protocols
The gelatin (GE) sponge was prepared as described previously (Ajioka et al., 2015) with some modification. Fifty microliters of 3% GE beMatrix Gelatin LS-H (Nitta Gelatin, Osaka, Japan) was added to each well of a 384-well plate and frozen at -20 C. The frozen GE samples were then lyophilized at 25 C, with centrifugation at 400 rpm (VC-96W; Taitek, Saitama, Japan). The freeze-dried GE samples were then crosslinked with 25 mM 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (Wako) in 90% acetone at room temperature overnight. After washing five times with double distilled water, the GE sponge was incubated in Neurobasal medium (GIBCO) for 3 h. Then, GE sponge was cut into blocks (1.2 3 1.2 3 1.2 mm 3 ) and conjugated with 10 mg/mL N-cadherin-Fc (IgG-Fc fused with the extracellular domain of mouse N-cadherin) or Fc solutions (Yue et al., 2010) for 24 h at 4 C.
+ 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!