The largest database of trusted experimental protocols

4 2 hydroxyethyl 1 piperazineethanesulfonic acid buffer

Manufactured by Thermo Fisher Scientific

4‐(2‐hydroxyethyl)‐1‐piperazineethanesulfonic acid buffer is a chemical compound commonly used as a buffering agent in biochemical and cell culture applications. It helps maintain a stable pH environment for various biological reactions and processes.

Automatically generated - may contain errors

4 protocols using 4 2 hydroxyethyl 1 piperazineethanesulfonic acid buffer

1

Canine Cancer Cell Lines

Check if the same lab product or an alternative is used in the 5 most similar protocols
Canine transitional cell carcinoma cells (K9TCC) was obtained from Prof. Knapp, Purdue (PU, Indiana, USA), canine osteosarcoma cell (Abrams) were obtained from Prof. Rebhurn, (UCD, California, USA) and canine hemangiosarcoma cells (DAL‐4) were obtained from Kerafast Inc. (Massachusetts, USA). The K9TCC and Abrams cells were grown in Dulbecco's modified eagle's medium (Gibco) containing 10% fetal bovine serum (FBS) (Gibco), 100 units/ml of penicillin (Gibco), 100 μg/ml of streptomycin (Gibco) and 10 mM of 4‐(2‐hydroxyethyl)‐1‐piperazineethanesulfonic acid buffer (Gibco) and incubated at 5% CO2 and 37°C. The three cell lines are described as TCC (transitional cell carcinoma, K9TCC), OSA (osteosarcoma, Abrams) and hemangiosarcoma (HSA, DAL‐4) in figures and text.
The DAL‐4 cells were grown in Ham F‐12 (Gibco) containing 10% FBS (Gibco), 100 μg/ml of primocin, 0.05 mg/ml of endothelial cell growth supplement, 0.1 mg/ml of heparin (Sigma‐Aldrich®), 10 mM of HEPES buffer (Gibco) and incubated at 37°C in 5% CO2 humidified incubator. All cell lines were free of mycoplasma.
+ Open protocol
+ Expand
2

Cell Culture Conditions for CHO, 293FT, and GD25 Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
CHO (Gu et al., 1999 (link); Xi et al., 2003 (link)), 293FT, and GD25 cells were cultured in DMEM complete (Cellgro) supplemented with 10% fetal bovine serum (FBS; Corning), 2 mM l-glutamine (Corning), 100 U/ml penicillin plus 100 μg/ml streptomycin (Corning), 1 mM sodium pyruvate (Gibco), 0.1 mM nonessential amino acids (Gibco), and 10 mM 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid buffer (Gibco). Cells were serum starved in DMEM containing each of the foregoing components except the FBS for at least 4 h before experiments.
+ Open protocol
+ Expand
3

Synthesis and Characterization of Gold Nanoparticles

Check if the same lab product or an alternative is used in the 5 most similar protocols
Gold(III) chloride trihydrate (HAuCl4·3H2O), trisodium citrate (Na3C6H5O7), tannic acid (C76H52O46), potassium carbonate (K2CO3), amino-undecanethiol (AUT), poly-ethyleneimine branched Mn2000 (PEI), 2-(N-morpholino)ethanesulfonic acid buffer solution (MES), sodium hydroxide (NaOH), hydrogen chloride (HCl), oligonucleotide model 600-800 bases (D1626), Sodium Phosphate Dibasic (Na2HPO4), Sodium phosphate monobasic (NaH2PO4), poly-L-lysine, Paraformaldehyde (PFA), Triton-X, Bovine Serum Albumin (BSA), Sodium Chloride (NaCl), and Calcium Chloride (CaCl2) were purchased from Sigma-Aldrich. Dulbecco’s Modified Eagle Medium (DMEM), Foetal Bovine Serum (FBS), Hoechst 3342 (H1399), Prolong antifade mounting medium (11559306), Optimem Medium, Pacific Blue-Annexin V, Propidium iodide (PI), accutase, 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid buffer (HEPES), and Prestoblue were purchased from Thermo Fisher. Phalloidin Alexa Fluor 647 (ab176759) was purchased from Abcam. Clean CAP eGFP mRNA (5 moU) was purchased from Tebu-Bio. TransIT®-LT1 Transfection Reagent was purchased from MirusBio. All chemicals were used as received without further purification. Distilled water passed through a Millipore system (ρ = 18.2 MΩ) was used in all experiments. All glassware was first rinsed with acetone and then with Millipore water before use.
+ Open protocol
+ Expand
4

Isolation and Stimulation of Nasal Stromal Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
Nasal stromal cells were isolated from NP single-cell suspensions by negative selection using anti-CD45 and anti-epithelial cell adhesion molecule microbeads (Miltenyi Biotec) to deplete hematopoietic and epithelial cells, as previously stated (30 (link), 31 (link)). The purity of the isolated cells was more than 95%, as shown in Supplementary Figure S1B.
Isolated nasal stromal cells were cultured overnight in Dulbecco’s Modified Eagle Medium (DMEM) with 1g/L D-Glucose medium (Thermo Fisher Scientific) supplemented with 1% penicillin and 1% streptomycin (Thermo Fisher Scientific), 0.05 mg/ml gentamicin (Thermo Fisher Scientific), 10 mM 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid buffer (Thermo Fisher Scientific), 2 mM L-glutamine (Thermo Fisher Scientific), and 10% FCS (GE Healthcare). Non-adherent cells were removed on the next day. The remaining cells were cultured for 2 days and non-adherent cells were removed again. Adherent cells were grown for an additional 2 days and then treated with human recombinant LTα1β2 at 1, 10, 100, or 1000 ng/ml (R&D Systems). After 12-h stimulation, cells were harvested for real-time PCR assay. After 48-h stimulation, cell culture supernatants were collected for ELISA.
+ 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!