Soluble Collagen Assay Kit (Fluorometric

Description: Cell adhesion is a complex process involved in migration/invasion, embryogenesis, wound healing and tissue remodeling. Cells adhere to the extracellular matrix, forming complexes with cytoskeleton components that can affect cell motility, differentiation, proliferation, and survival. Our CytoSelect 48-Well Cell Adhesion Assays provide a fully quantitative method for the evaluation of cell adhesion. The 48-well plate is precoated with Collagen IV.

Description: Our Soluble Collagen Assay Kit detects soluble collagen in cell and tissue lysates. This assay uses a Sirius Red Reagent to stain the triple helix structure of collagen that has been dried onto the wells of a 96-well plate. The collagen is washed with an Acidic Reagent and the stain is eluted with a Basic Reagent, which is then transferred to a new plate and read colorimetrically between 540nm-560nm. The amount of soluble collagen in samples is determined based on a provided collagen standard curve.

Description: Assay Kit for detection of GST activity in the research laboratory

Description: Our Starch Assay Kit (Fluorometric) measures starch in food samples. First, starch is broken down into glucose monomers by amyloglucosidase. Glucose is then oxidized by glucose oxidase, producing D-gluconic acid and hydrogen peroxide. The hydrogen peroxide reacts specifically with the kit?s Fluorometric Probe and is detected at ex. 530-570 nm/em. 590-600 nm. Starch levels in unknown samples are determined based on the provided starch standard curve.

Description: Our Lactate Assay Kit measures L-lactate in biological samples. Lactate is first oxidized by lactate oxidase, yielding pyruvate and hydrogen peroxide. The hydrogen peroxide released from this reaction is specifically detected by either a colorimetric or fluorometric probe in a 1:1 ratio. Lactate levels in unknown samples are determined based on a lactate standard curve.

Description: Cell Biolabs? Choline Assay Kits are simple assays that measure the amount of choline present in a variety of sample types in a convenient 96-well microtiter plate format.  Each kit provides sufficient reagents to perform up to 96 assays, including blanks, acetylcholine standards and samples.  Sample choline concentrations are determined by comparison with a known choline standard and measured on a fluorescence plate reader.

Description: Cell Biolabs? Alcohol Assay Kits measure primary alcohols by an enzymatic, oxidation reaction, producing hydrogen peroxide which reacts with the kit?s probe. These assay kits come in either colorimetric or fluorometric. The colorimetric assay has a detection sensitivity limit of ~30 µM (0.0001 % w/v) and the fluorometric has a detection sensitivity limit of ~15 µM (0.00007 % w/v). They can detect various primary alcohols and are not ethanol specific.

Description: The Glucose Assay Kit (Fluorometric) measures total glucose present in food or biological samples. Glucose Oxidase first oxidizes glucose, generating hydrogen peroxide that is detected by a fluorogenic probe.

Description: Our Glycogen Assay Kit (Colorimetric) measures glycogen in serum, plasma, urine, lysates, and cell culture supernatants. First, glycogen is broken down into glucose monomers by amyloglucosidase. Glucose is then oxidized by glucose oxidase, producing D-gluconic acid and hydrogen peroxide. The hydrogen peroxide reacts specifically with the kit?s Colorimetric Probe and is detected with a spectrophotometric plate reader at 540-570nm. Glycogen levels in unknown samples are determined based on the provided glycogen standard curve.

Description: Our Phosphate Assay Kit (Fluorometric) measures total inorganic phosphate present in lysates, solutions, food, or biological samples in a 96-well fluorescence-based plate reader. 1000 assays/kit.

Description: Our NAD+/NADH Assay Kit detects NAD+ and NADH in cell and tissue lysates. Total NAD+/NADH can be detected or samples can be treated with an acid or base treatment to specifically detect NAD+ or NADH. This assay uses an enzymatic cycling reaction that reduces NAD+ to NADH, which then reacts with a fluorometric probe and is detected with a fluorescence plate reader at 530-570nm excitation and 590-600nm emission. NAD+/NADH levels in unknown samples are calculated based on the provided NAD+ standard curve.

Description: Assay Kit for detection of Phosphate in the research laboratory