resDetect™ Gentamicin ELISA Kit

제품 세부정보

Assay Type	Competitive-ELISA
Analyte	Gentamicin
Format	96T (8×12 strips)
Regulatory Status	RUO
Sensitivity	0.25 ng/mL
Standard Curve Range	0.25 ng/mL-8 ng/mL
Assay Time	1 h 20 min
Suitable Sample Type	For the detection and quantitative determination of Gentamicin residues in plasmid DNA raw materials for cell and gene therap.
Sample volume	50 μL

Product Overview
Gentamicin ELISA Kit is based on the ELISA competitive method and is used to detect and quantitatively determine Gentamicin residues in plasmid DNA raw materials, proteins for CGT, vaccines, and other biological drugs. The kit is calibrated against NIFDC and USP standards to ensure accuracy and regulatory compliance, and is designed to provide a reliable solution for monitoring and controlling Gentamicin residues in the production of biological products, helping to ensure drug safety. It can also be used as a universal detection tool for the quantitative determination of Gentamicin.
Reconstitution
Please see Certificate of Analysis for details of reconstitution instruction and specific concentration.
Storage
1. The kit is stable for 24 months from the date of manufacture if stored at 2°C to 8°C.
2. The reconstructed Gentamicin standard is stored at -70°C in at least 300ul per tube and cannot be frozen or thawed repeatedly.
3. Do not use reagents past their expiration date.

ID	Components	Size
RES-A025-C01	Gentamicin Coated Plate	1 plate (8×12 strips)
RES-A025-C02	Gentamicin Standard	0.1152 μg
RES-A025-C03	HRP-Anti-Gentamicin Antibody	6 mL
RES-A025-C04	1×Dilution Buffer	50 mL
RES-A025-C05	20xWashing Buffer	50 mL
RES-A025-C06	Substrate Solution	12 mL
RES-A025-C07	Stop Solution	7 mL

Typical Data
Please refer to DS document for the assay protocol.
Serial dilutions of gentamicin (from 8 ng/mL to 0.25 ng/mL) was added into gentamicin: anti-gentamicin binding reactions. The assay was performed according to the protocol dscribed below. Background was subtracted from data points prior to log transformation and curve fitting (QC tested).

연락하기

신약 후보물질 라이선싱