Endotoxin

The main component of Control Standard Endotoxin is E. coli endotoxin, whose efficacy has been calibrated according to national standards for bacterial endotoxin. It is used for TAL / LAL reagent sensitivity review, interference test and various positive controls in bacterial endotoxin test, and can be used for quantitative method. It is installed in a Vial bottle or ampoule and can be dissolved and used without endotoxin water, which is convenient and quick.

The endotoxin indicator is used in the GMP verification of dry heat sterilization equipment of pharmaceutical manufacturers and the endotoxin interference experiment of medical devices. Confirm the heat distribution at different locations in the cavity of the tunnel oven and dry heat incubator, and confirm whether the original sterilization and heat removal procedures can meet the pre-design requirements.

Bacterial endotoxin test water is used for endotoxin detection and reagent removal configuration.

Creative BioMart offers these products in various specifications.

Origin: E.coli O111:B4
Forms: Liquid
Storage: 2-8 ℃
Principle: Gel Clot LAL
Origin: E.coli O111:B4
Forms: Lyophilized powder
Storage: 2-8 ℃
Principle: Gel Clot LAL
Origin: E.coli O111:B4
Forms: Lyophilized powder
Storage: 2-8 ℃
Principle: Gel Clot LAL
Origin: E.coli O111:B4
Forms: Lyophilized powder
Storage: 2-8 ℃
Principle: Turbidimetric LAL Assay
Origin: E.coli O111:B4
Forms: Lyophilized powder
Storage: 2-8 ℃
Principle: Gel Clot LAL
Origin:
Forms: Liquid
Storage: 2-8 ℃
Principle:
Origin:
Forms: Liquid
Storage: 2-8 ℃
Principle:
Origin:
Forms: Liquid
Storage: 2-8 ℃
Principle:
Origin:
Forms: Liquid
Storage: 2-8 ℃
Principle:
Origin:
Forms: Liquid
Storage: 2-8 ℃
Principle:

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