The largest database of trusted experimental protocols

5 protocols using l galactose

1

Enzymatic Synthesis of Sugar Lactones

Check if the same lab product or an alternative is used in the 5 most similar protocols
All
chemicals and buffers were purchased
from Sigma-Aldrich, unless otherwise specified. Sugar lactones that
were not commercially available were synthesized according to standard
published procedures with the exception of 4-deoxy-l-fucono-1,5-lactone,
which was enzymatically synthesized.13 (link),14 (link) The noncommercial
lactones included the following: l-fucono-1,4-lactone, d-arabinono-1,4-lactone, l-xylono-1,4-lactone, l-mannono-1,4-lactone, d-talono-1,4-lactone, d-allono-1,4-lactone, l-rhamnono-1,4-lactone, d-lyxono-1,4-lactone, l-lyxono-1,4-lactone, l-arabinono-1,4-lactone, d-xylono-1,4-lactone, l-mannono-1,5-lactone, l-rhamnono-1,5-lactone, and 4-deoxy-l-fucono-1,5-lactone.
The sugar lactones that were obtained from either CarboSynth or ChromaDex
included the following compounds: l-galactono-1,4-lactone, d-mannono-1,4-lactone, d-galactono-1,4-lactone, d-ribono-1,4-lactone, d-glucurono-6,3-lactone, d-erythronolactone, and l-glucono-1,5-lactone. Aldose
sugars were obtained from either Sigma-Aldrich or Carbosynth and included l-fucose, l-galactose, l-glucose, d-altrose, d-arabinose, l-xylose, l-rhamnose, d-mannose, l-allose, d-talose, l-talose, d-allose, d-galactose, l-mannose, d-gulose, d-glucose, l-arabinose, l-ribose, d-lyxose, l-lyxose, d-xylose, d-ribose,
and 4-deoxy-l-fucose.
+ Open protocol
+ Expand
2

Analytical Standards for Phytochemical Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
ACS-grade methanol for extraction, LC-MS OptimaTMacetonitrile, and UHPLC-MS/MS OptimaTM grade solvents (water, acetonitrile, methanol) were from Fisher (Thermo Fisher Scientific, Nepean, ON, Canada). SupraPurTM formic acid (98%–100%) and ACS grade isopropyl alcohol were from VWR (VWR International LLC, Mississauga, ON, Canada). Commercially available analytical standards were sourced from Extrasynthese (Genay, Cedex, FR) (quercetin-3-O-glucoside ≥ 99%; kaempferol-3-O-rutinoside ≥ 98%; quercetin-3-O-rhamnoside ≥ 98.5%) or Sigma-Aldrich (St. Louis, MO, USA) (quercetin-3-O-rutinoside ≥ 95%; kaempferol-3-O-glucoside ≥ 97%; xanthohumol ≥ 96%; quercetin-3-O-(6’’-O-malonyl)-glucoside ≥ 85%). International Calibration Extract 3 (ICE-3), an alpha & beta acid standardized mixture, was sourced from Labor Veritas (AG, Zurich, CZ). Deuterated solvent (DMSO-d6) was from CIL (Cambridge Isotope Laboratories Inc., Tewksbury, MA, USA). Pyridine, o-tolyl isothiocyanate, L-cysteine methyl ester, D-glucose, L-glucose, D-galactose, L-galactose were purchased from Sigma-Aldrich.
+ Open protocol
+ Expand
3

Monosaccharide Identification and Antioxidant Assay Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
The monosaccharide standards (D-mannose, D-rhamnose, glucuronic acid, galacturonic acid, D-glucose, L-arabinose, and L-galactose), 1-phenyl-3-methyl-5-pyrazolone (PMP), 2, 2-diphenyl-1-picryl-hydrazyl (DPPH), 2, 2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), and lipopolysaccharide (LPS) were purchased from Sigma-Aldrich Co. (St. Louis, MO, USA). Zinquin ethyl ester was purchased from Biotium, Inc. (Fremont, CA, USA). DEAE-52 was purchased from Whatman Co. (UK). Sephadex-G 100 was purchased from Solarbio Co. (Beijing, China). Zn Standard Solution (99.999%) was purchased from SPEX CertiPrep Co. (USA). The diagnostic kit for reactive oxygen species (ROS) was purchased from Nanjing Jiancheng Bioengineering Institute (Nanjing, China). All other chemicals were of analytical grade from local chemical suppliers in China.
+ Open protocol
+ Expand
4

Maintenance of Ar. subalbatus and Microbe Strains

Check if the same lab product or an alternative is used in the 5 most similar protocols
Ar. subalbatus used in this study were maintained at the University of Missouri- Columbia following the methods described previously (Beerntsen et al., 1989 (link); Wang et al., 2012 (link)).
Gram-positive Staphylococcus aureus, Bacillus subtilis, B. cereus, and M. luteus, Gram-negative E. coli DH5α, Serratia marcescens, Pseudomonas aeruginosa, and yeast Saccharomyces cerevisiae were originally from ATCC or Sigma and maintained in the laboratory. Smooth LPS from E. coli 055:B5 and 026:B6, S. marcescens, P. aeruginosa, Salmonella enterica, rough mutants of LPS from E. coli EH100 (Ra-LPS), E. coli F583 (Rd-LPS), E. coli J5 (Rc-LPS), and S. enterica serotype minnesota Re 595 (Re-LPS), mono-phosphoryl lipid A from E. coli F583 (Rd mutant), and di-phosphoryl lipid A from E. coli F583 (Rd mutant), laminarin (β-1,3-glucan), curdlan, mannan, zymosan (from S. cerevisiae), D-galactose, L-galactose, N-acetyl-D-galactosamine (GalNac), D-glucose, L-fucose, L-rhamnose, talose, xylose, lactose, sucrose, maltose, melibiose, chitotriose were all from Sigma-Aldrich (MO, USA). TLR grade LPS-K12 and PG-K12 from E. coli K12, PG-SA and LTA-SA from S. aureus, and PG-BS and LTA-BS from B. subtilis were from Invivogen (CA, USA).
+ Open protocol
+ Expand
5

Carbohydrate Solutions for Injection

Check if the same lab product or an alternative is used in the 5 most similar protocols
The following carbohydrates, all from Sigma Aldrich (St Louis, MO) were prepared as 10 mg/ml solutions in deionized H2O (dH2O): λ carageenan, dextran sulfate (sodium salt from Leuconostoc spp.), fucoidan (crude, from Fucus vesiculosus), L-fucose, L-galactose, heparin (sodium salt from porcine intestinal mucosa), and laminarin from Laminaria digitata. Carageenan was heated to 50 °C prior to uptake into the injection needle in order to reduce viscosity, and was allowed to cool for several minutes before injection.
+ 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!