DESCRIPTION

Used for the quantitative determination of Conatumumab concentration in serum and plasma.

PRINCIPLE OF THE ASSAY

This assay employs the quantitative sandwich enzyme immunoassay technique. A capture reagent specific for Conatumumab has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any Conatumumab present is bound by the immobilized reagent. After washing away any unbound substances, a detection reagent is added. Following a wash, a substrate solution is added and color develops in proportion to the amount of Conatumumab bound. The color development is stopped and the intensity of the color is measured.

SPECIFICATIONS

Catalog No.	ADA0004
Size	96 T
Detection method	Colorimetric
Assay type	Quantitative, sandwich ELISA
Sample type	Serum, Plasma
Range	78.13 - 5,000 ng/mL
Sensitivity	91.95 ng/mL
Shipping	2 - 8℃
Storage	2 - 8℃
Validity	6 months

PRECISION

Intra-assay precision (within an assay): CV < 20%. Inter-assay precision (between assays): CV < 20%.

RECOVERY

Recovery of Conatumumab spiked into serum and plasma samples ranged from 80% to 120%.

STABILITY AND STORAGE

Shipping condition 2 - 8℃. Store the kit at 2 - 8℃ upon receipt. The stability of the kit is determined by the loss rate of activity, which is less than 10% prior to the expiration date under appropriate storage conditions.

PRECAUTIONS

1. This product is for research use only. It is not intended for diagnostic or therapeutic use.

2. Bring all reagents and samples to room temperature before use. Refrigerate reagents immediately after use.

3. Avoid repeated freeze-thaw cycles of samples and standards.

4. Wear protective gloves and follow standard laboratory safety procedures.