The largest database of trusted experimental protocols

7 protocols using hydrazine sulfate

1

Arsenic Determination in Rice Flour

Check if the same lab product or an alternative is used in the 5 most similar protocols
Nitric acid (HNO3) and hydrochloric acid (HCl) were purchased from Merck (Darmstadt, Germany). Dimethylarsinic acid (DMA), hydrazine sulfate, hydrobromic acid, and other chemicals were purchased from Sigma-Aldrich (St. Louis, MO, USA). Rice flour (standard reference material [SRM] 1568a) was obtained from the National Institute of Standards and Technology (Gaithersburg, MD, USA). All standard solutions, reagents, and samples were prepared using deionized water (18 MΩcm). To avoid arsenic residue contamination, all glassware was soaked in 10% (v/v) HNO3 overnight and washed three times with deionized water before use.
+ Open protocol
+ Expand
2

Betulin Extraction from Birch Bark

Check if the same lab product or an alternative is used in the 5 most similar protocols
Betulin was isolated from Betula Pendula bark using the methods in [26 (link)]. 5-fluorouracil (Sigma Aldrich, Moscow, Russia), hydrazine sulfate (Sigma Aldrich), purified water (resistivity ≥18 MΩ·cm, Millipore, Merck, Darmstadt, Germany).
+ Open protocol
+ Expand
3

Lactic Acid Analysis in Oral Biofilms

Check if the same lab product or an alternative is used in the 5 most similar protocols
Among the final products of oral microorganisms, lactic acid was analyzed because it is the strongest acid metabolite, presenting a pKa (acid dissociation constant) of 3.810. In the fifth day of the biofilm growth process, the medium was renewed and the plates were incubated for further 3.5 h. Lactic acid analysis was carried out in the culture media (BHI broth).
The amount of lactic acid was determined by the enzymatic method13. In 96-wells plates, 85 mL of 1 mol/L glycine (Sigma Aldrich, Saint Louis, Missouri, USA), 85 mL of 0.8 mol/L hydrazine sulfate (Sigma Aldrich, Saint Louis, Missouri, USA), 20 mL of 26 mmol/L b-nicotinamide adenine dinucleotide (Sigma Aldrich, Saint Louis, Missouri, USA) and 10 mL of BHI broth or L-lactic acid standards (0.2 to 3.0 mmol/L; Sigma Aldrich, Saint Louis, Missouri, USA) were added. The absorbance was read at 340 nm (A1). Then, 10 mL of 1.0 g/L L-lactic dehydrogenase were added. After 1 h at room temperature, a new reading was performed at 340 nm (A2). The quantity of lactic acid (DL) was obtained by the equation DL=A2-A1. The DL values were converted to mmol/L of lactic acid, according to the readings of L-lactic acid standards.
+ Open protocol
+ Expand
4

Lactate Biosensor Development Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
Delignified cellulose (Greencel) was obtained from Bukoza and was used without any additional pre-treatment. L-lactate oxidase (EC 1.1.3.2, LOx) from Pediococcus sp. with specific activity ≥ 20 U·mg−1 solid, Nafion®, hemin, guaiacol, hydrazine sulfate, L-lactate, HAuCl4, and H2PtCl6 were obtained from Sigma-Aldrich. In addition, 28% ammonia solution, Na2HPO4, CaCl2, KН2РО4, HNO3, and sodium citrate were purchased from Merck, and 30% H2O2 from Thermo Fisher Scientific. All reagents and solutions were prepared using ultrapure water.
+ Open protocol
+ Expand
5

Enzymatic Assays for Enolase and Aldolase

Check if the same lab product or an alternative is used in the 5 most similar protocols
Enolase activity was measured directly by monitoring the formation of Phosphoenol pyruvate (PEP) using SPECTRAmax PLUS 384 (Molecular Devices Corp.) at 240 nm as described earlier [31] (link). The assay was performed at 25°C in a 1.0 mL reaction mixture containing 20 mM Tris–HCl, pH 7.5, 2 mM MgSO4, 75 mM KCl and 1 mM 2-phosphoglycerate (2PGA) or 2 mM PEP. For the determination of the values of kinetic parameters, the substrate concentrations were varied from 0 to 10 mM for 2PGA and 0 to 7.5 mM for PEP.
Aldolase activity was measured by using hydrazine assay modified by Jagannathan et al[32] (link) using D-Fru-1,6-P2 (Sigma) as substrate and hydrazine sulfate (Sigma) as detection reagent for the formed 3-phosphoglyceraldehyde. The assay was performed in a 1.0 mL reaction mixture and the absorbance was recorded at 240 nm. To calculate Vmax and Km, the activity was measured between 0.1 and 7 mM D-Fru-1, 6-P2.
+ Open protocol
+ Expand
6

PF4 Interaction with Heparin and Enoxaparin

Check if the same lab product or an alternative is used in the 5 most similar protocols
HP and LMWH (enoxaparin) were obtained from the United States Pharmacopoeia convention. Recombinant human PF4 was purchased from Sino Biological (Beijing, China). NHS-LC-LC-Biotin was purchased from Thermo Fisher Scientific (Shanghai, China). Deuterium oxide (99.9% D2O) was obtained from Qingdao Tenglong Weibo Technology Co., Ltd. (Qingdao, China). The 70% aqueous hydrazine was obtained from Sinopharm Chemical Reagent Co., Ltd. (Shanghai, China). Hydrazine sulfate, dimethyl sulfoxide, pyridine and Dowex 50WX8 (hydrogen form, 50 to 100 mesh) were purchased from Sigma-Aldrich (Shanghai, China). N, O-bis(trimethylsilyl)acetamide (BTSA) was obtained from Jinming Biotechnology (Beijing, China). Phosphate-Buffered Saline (PBS) was purchased from Wuhan Procell Biological Technology (Wuhan, China).
+ Open protocol
+ Expand
7

Cytotoxicity Evaluation of Metronidazole

Check if the same lab product or an alternative is used in the 5 most similar protocols
3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT; Sigma, Saint Louis, USA), hydrazine sulfate, ammonium heptamolybdate tetrahydrate, ammonium acetate, acetic acid, tetrabutylammonium bromide (TBAB), cetyltrimethylammonium bromide (CTAB), methyl methacrylate (MMA), benzoyl peroxide (BPO), and all of the used solvents were purchased from Sigma-Aldrich or some of the other chemical companies. All of the other chemicals were analytical grade and applied without further purification. Metronidazole (MTN) was purchased from Amin pharmacy (Iran).
+ 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!