The largest database of trusted experimental protocols

Re301

Manufactured by Yamato Scientific
Sourced in Japan

The RE301 is a digital rotary evaporator designed for laboratory use. It is equipped with a digital temperature display and control, allowing for precise temperature monitoring and adjustment during the evaporation process. The RE301 features a boiling flask capacity of up to 3 liters and a rotation speed range of 20 to 280 rpm.

Automatically generated - may contain errors

Lab products found in correlation

5 protocols using re301

1

Pectin Yield Determination from RDF-PP

Check if the same lab product or an alternative is used in the 5 most similar protocols
The pectin yield (PY) of RDF-PP was determined using the method described by Zahari et al. [24 (link)]. In an ISO glass bottle, RDF-PP was extracted with water in a 1:50 (w/v) ratio at pH 2.0 ± 0.03 using citric acid with continuous stirring at 150 rpm in a water bath (MaXturdy 18, Daihan Scientific, Gangwon-do, Korea) at 68 ± 0.4 °C for 77 min. After cooling, the suspension was filtered (Whatman N° 113) and concentrated to 50% of its initial volume in a rotary evaporator (RE301, Yamato Scientific, Tokyo, Japan) at 55 °C, 81 rpm, and 90 kPa. For the precipitation of pectin, 96% ethanol (v/v) was added to the concentrated solution at a 1:2 (v/v) ratio, and the mixture was kept at 4 °C overnight. Next, the uppermost pectin layer was subjected to filtration and underwent a series of three washes using ethanol solutions at 50, 75, and 100%. Then, the retained pectin was dried in an oven at 50 °C until constant weight, cooled, ground, and weighed. The PY was calculated using the following equation: PY%=PWi×100
where ‘P’ represents the weight of dried pectin (g) and ‘Wi’ represents the initial weight of the sample (g).
+ Open protocol
+ Expand
2

Extraction of Phenolic Compounds from Tropical Fruits

Check if the same lab product or an alternative is used in the 5 most similar protocols
In this study, the fruits were harvested from a family vegetable garden in Obregon, Mexico, transferred to the Emergent Technologies Laboratory at the Technological Institute of Sonora. The fruits were washed and the edible part were separated and stored in a freezer (−20 °C) until analysis.
Extraction of phenolic compounds was performed according to the method proposed by Suárez, et al. [37 (link)] with some modifications. A representative portion of fruits (8 g) was homogenized in 40 mL of water, water:ethanol (20:80, v/v) or water:methanol (20:80, v/v) at 250 rpm using ultra-turrax T18 basic homogenizer (Ika Works Inc., Wilmington, NC, USA). The water and the mixture water:ethanol were selected as solvents because these fruits are consumed as fruit water but their peel or the whole fruit might be used to obtain ethanol-based tinctures for therapeutic purposes, as reported for other small fruits [38 ]. The mixture water: methanol (20:80, v/v) is highly used for the efficient liberation of phenols from vegetable foods [39 (link)]. The extracts were vacuum filtered through Whatman #1 paper, the solvent was evaporated in a rotary evaporator (RE301, Yamato, Santa Clara, CA, USA) at 30 °C, and the residue was stored at 4 °C until further analysis. Six extracts were obtained for each fruit type (red and yellow mombin).
+ Open protocol
+ Expand
3

Ethyl Acetate Fraction Preparation: Detailed Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
The ethyl acetate fraction was prepared using a liquid–liquid extraction method. The previous study used maceration in the extraction of crude ethanol extract [10 (link)]. Fifty grams of the ethanol extract was suspended in 200 mL of ethanolic water (1:1). Hereafter, the extract was fractionated with 200 mL of n-hexane in a separating funnel, and was shaken consecutively. It was then allowed to stand until it forms two layers. The n-hexane fraction in the lower layer was separated into Erlenmeyer. This process was repeated three times to produce a colorless n-hexane fraction. Furthermore, the ethanol residue was re-fractionated using ethyl acetate solvent in the same way as the n-hexane. The fractions were combined and concentrated using a rotary evaporator (Yamato® RE301) to obtain n-hexane, ethyl acetate, and ethanol fractions [11 (link)]. Finally, the ethyl acetate fraction was used to test diuretic activity.
+ Open protocol
+ Expand
4

Formulation and Characterization of AGCL

Check if the same lab product or an alternative is used in the 5 most similar protocols
The formulation of AGCL was based on alkyl glucose and the glucose structural fragments were modified into the membrane structure of liposomes. Liposomes with this structural feature could effectively be recognized by GLUT1 of tumor cells. The thin film dispersion method was used to prepare AGCL. The preparation steps and methods were as follows: dissolution, hydration, ultrasonication and filtration [22] (link). (1) 21.6 mg Cel, 240 mg SC95, 9 mg cholesterol, 28 mg DSPE-mPEG2000 and 26 mg N-octyl-β-d-glucopyranoside were placed into 50 ml round bottom flask, the flask was filled with 15 ml of anhydrous ethanol to completely dissolve all the ingredients. But CL didn't contain N-octyl-β-d-glucopyranoside. (2) A rotary evaporator (RE301, YAMATO, Japan) was used to evaporate anhydrous ethanol under reduced pressure at 50 °C, after that 23.6 ml purified water was added and the solute film was hydrated for 25 min to obtain the primary Cel liposomes solution. (3) The primary liposomes solution was treated with 450 w ultrasound for 2 min. (4) The primary liposomes were filtered by 0.22 µm membrane to obtain the AGCL.
+ Open protocol
+ Expand
5

Extraction of Bioactive Compounds from Annona muricata Leaves

Check if the same lab product or an alternative is used in the 5 most similar protocols
The leaves of A. muricata L. were obtained from 9-year-old tree crops in San Blas, Nayarit, Mexico. The material was dried at 45 °C for 24 h in a Blinder oven (model ED 115) and then powdered and passed through a sieve (number 20). The AEE was obtained using 10 g of dried leaves mixed with 150 mL of 90% ethanol and 10% acetic acid (9:1), which was macerated with agitation in complete darkness for 72 h. The extract was concentrated in a rotatory evaporator (RE301; Yamato, Japan). For the AE, 10 g of dried leaves were mixed with 150 mL of distilled water and boiled for 5 min; then the extract was filtered and concentrated as previously described.
+ 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!