The largest database of trusted experimental protocols

3 protocols using magnesium chloride

1

Glycoprotein Purification and Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Toyopearl AF-Formyl-650M resin was from Tosoh Bioscience (King of Prussia, PA, USA). Wheat germ agglutinin (WGA) was purchased from Vector Laboratories (Burlingame, CA, USA). Stainless steel columns (2×250 mm) and the Gemini C18 column were obtained from Phenomenex (Torrance, CA, USA). Ovomucoid (type III-O, free of ovoinhibitor), trypsin (TPCK treated), PNGase F, chloroform, NaOH beads (97% purity), iodomethane, 2-mercaptoethanol, dithiothreitol, iodoacetamide, trizma base, and sodium cyanoborohydride (NaCNBH3) were all purchased from Sigma-Aldrich (St. Louis, MO, USA). Water and acetonitrile (ACN) were obtained from EMD Chemicals (Darmstadt, Germany). Formic acid was from Alfa Aesar (Ward Mill, MA, USA). Trifluoroacetic acid (TFA), dimethylformamide (DMF), urea, ammonium bicarbonate, sodium chloride, magnesium chloride, and calcium chloride were all from Mallinckrodt Pharmaceuticals (St. Louis, MO, USA). C18 Zip-tips were from Agilent Technologies (Santa Clara, CA, USA). C18 Sep-Pak cartridges were from Waters (Milford, MA, USA). Empty spin columns were purchased from Harvard Apparatus (Holliston, MA, USA).
+ Open protocol
+ Expand
2

Anaerobic Protein Crystal Growth

Check if the same lab product or an alternative is used in the 5 most similar protocols
Protein stocks consisted of 30–35
mg/mL protein in a solution of 200 mM sodium chloride, 50 mM Tris/HCl
at pH 7.75, and 5 mM sodium dithionite. Protein crystals were grown
in 24-well plates using the sitting-drop method with a 1:1 ratio of
protein stock to reservoir solution at room temperature in an anaerobic
chamber with an atmosphere of ∼95% argon and ∼5% hydrogen.
All solutions were made anaerobic through a series of vacuum and argon
cycles. The reservoir solution for Av1 crystals consisted of double-distilled
water, 15% polyethylene glycol (MW 4000 g/mol, Hampton Research),
0.5–0.8 M sodium chloride (VWR), 0.2 M imidazole/malate at
pH 8 (Sigma-Aldrich), and 5 mM sodium dithionite (J.T. Baker). The
reservoir solution for Cp1 crystals consisted of double-distilled
water, 13.5–14% polyethylene glycol (MW 3350 g/mol, Hampton
Research), 0.3–0.5 M magnesium chloride (Mallinckrodt), 0.08
M Tris/HCl at pH 8 (Fisher Scientific), and 5 mM sodium dithionite.
Av1 and Cp1 crystals of block morphology formed overnight.
+ Open protocol
+ Expand
3

Thiolated Oligonucleotides for Graphite-based Biosensors

Check if the same lab product or an alternative is used in the 5 most similar protocols
All thiolated oligonucleotides used in this study were purchased from Integrated DNA Technologies (Coralville, IA). Graphite powder (99%, 7–11 μM) was purchased from Alfa–Aesar (Heysham, Lancashire, UK). Sulfuric acid, phosphoric acid, hydrogen peroxide, trisodium citrate, sodium phosphate tribasic, sodium phosphate dibasic, boric acid, tetrachloroauric acid, dimethyl sulfoxide, apigenin, xylene, ethanol, 3,3-diaminobenzidine tetrahydrochloride, hematoxylin, and isopropanol were purchased from Sigma–Aldrich (Milwaukee, WI). Citric acid, calcium chloride, magnesium chloride, potassium permanganate, tris(hydroxymethyl)aminomethane (Tris), and hydrochloric acid were purchased from Mallinckrodt Baker (Phillipsburg, NJ). Alpha-MEM and fetal bovine serum were purchased from GIBCO (Campinas, Brazil). An MTT assay kit was purchased from Thermo Fisher Scientific (Waltham, MA). MUC1 (VU4H5) mouse mAb, anti-mouse IgG, and HRP-linked antibody were purchased from Cell Signaling Technology (Danvers, MA). Milli-Q ultrapure water (18 MΩ, Millipore, Billerica, MA) was used in all experiments.
+ 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!