Fluorescence Assay Gpcr

Description: a total assay solution for multi-well plate-based, high-throughput measurements of Gi/o GPCR agonism measured via native GIRK coupling.

Description: This product includes 60 ul of 1000 x PSA dye for more than 200 assays with the assay volume of 0.3 ml using 96-well plates or cuvettes.

Description: Cell Cycle

Description: Cell Cycle

Description: It includes 550 µl of 10 x Buffer, 110 µl of 10 x DNA and 110 µl of 10 x Dye B22.

Description: Our Cell Meter™ assay kits are a set of tools for monitoring cell viability.

Description: Autophagy is an evolutionarily conserved degradation process that targets long-lived proteins, organelles, and other cytoplasmic components for degradation via the lysosomal pathway.

Description: This Cell Meter™ Autophagy Kit employs Autophagy Green™ as a specific autophagosome marker to analyze the activity of autophagy.

Description: RNases are a class of hydrolytic enzymes that catalyzes both the in vivo and in vitro degradation of ribonucleic acid (RNA) molecules into smaller components. RNase enzymes are categorized into two groups: exoribonucleases and endoribonucleases. RNases are ubiquitous in the environment, and in some biological materials, they are present in relatively high concentrations. RNases also frequently contaminate common molecular biological reagents such as reaction buffers, enzymes such as reverse transcriptase and RNA polymerase, and buffers for RNA purification and storage. It is often used DEPC and/or heaten to remove RNases from containers in experiments. Since even only minute amounts of RNase contamination would ruin the experiment, it is necessary to evaluate the presence of RNase with the RNase Activity Assay Kit (Fluorescence).

Description: Deoxyribonucleases (DNases) are enzymes which are able to hydrolyze phosphodiester bonds of DNA molecules. They can be divided into two families, which differ in biochemical and biological properties—DNase I and DNase II families. The presence of DNases would affect many experimental results like PCR, so it is necessary to evaluate the presence of DNases.DNases are ubiquitous in both the environment and many biological materials. Many molecular biology experiments rely on the use of plastics, chemicals, and solutions that are free from detectable DNase activity, once these materials are contaminated with DNases, the experiments will be affected because of the DNases can degrade DNA. Since even only minute amounts of DNase contamination would ruin the experiment, it is necessary to evaluate the presence of DNase with a reasonable method.Published methods for detecting DNase such as Nucleic acid hydrolyzed gel electrophoresis and ultraviolet spectrophotometer are typically time consuming, not quantitative, and relatively insensitive. The other methods such as HPLC and electrochemical methods are limited to instrumentation. In contrast, the DNase Activity Assay Kit (Fluorescence) can detect DNase contamination within 30 minutes, and the kit is high sensitivity, easy to use. Moreover, the DNase and RNase Activity Assay Kit (Fluorescence) have been designed to work together seamlessly for simultaneous quantitative detection of DNases and RNases in a single sample.

Description: ADP is involved in many biological reactions such as protein kinases.

Description: Nicotinamide adenine dinucleotide (NAD+) and nicotinamide adenine dinucleotide phosphate (NADP+) are two important cofactors found in cells.

Description: Nicotinamide adenine dinucleotide (NAD+) and nicotinamide adenine dinucleotide phosphate (NADP+) are two important cofactors found in cells.