High-Throughput DNA Isolation MO BIO Laboratories providing innovative molecular biology research tools for FFPE DNA, RNA, Protein From Soil, DNA Extraction and RNA Purification. About MO BIO Laboratories Inc., a privately held company located in the San Diego biotech corridor (Carlsbad, CA, USA), was founded in 1993 by Liz and Mark Brolaski. Initially a small business start-up, MO BIO has grown into a multi-million dollar operation with international production, research, and distribution. Today, MO BIO's growth and customer loyalty is challenging some of the world's leading molecular biology tool companies with innovative technologies and a commitment to value. industry. Mo Bio innovation MO BIO is known as the World Leader in Soil DNA & RNA Isolation®, thanks to its patented Inhibitor Removal Technology®, which enables isolation of pure DNA from challenging samples like soil, water, plants and stool. Thus, MO BIO kits are the method of choice for microbiome projects, as these studies often require isolation of nucleic acids from challenging samples that contain a variety of PCR inhibitors Mo Bio Philosophy MO BIO’s founders and employees are dedicated to the preservation of the environment and to bettering the quality of the Earth through science. MO BIO’s team of scientists is committed to developing innovative tools for researchers that require pure, high quality nucleic acids for use in next generation sequencing and other downstream applications. It is MO BIO’s aim to make scientists’ working life more productive and efficient, in order to give them time to focus on what is critical, not only at work, but in life. Endotoxin-Free Certification This certification follows USP chapter <85> and ANSI/AAMI ST72:2011 guidelines and FDA regulations to certify any of a variety of products to be free of contaminating endotoxins or to quantify endotoxin levels. Protease-Free Certification This test certifies any of a wide variety of products to be free of protease contamination. Bioburden The Bioburden test is used to test for the viable microbial load of a given product. Bioburden testing is the inventory and microbial characterization of the viable microorganisms on or in a medical device, component, raw material, or package. Bioburden testing is usually performed as part of a sterilization program, and is done on any product that requires control and monitoring of bioburden counts. This test can serve several purposes, including identifying potential production issues that can result in insufficient sterilization. Radiation Sterilization Validation This test follows current AAMI method 1 guidelines to calculate the appropriate irradiation dose needed to sterilize any of a wide range of products. This test also includes a validation of the calculated irradiation dose that is delivered to the product. Quarterly Dose Audits (QDA) are established using this validation. Radiation sterilization is the exposure of a material, object, or body to ionizing radiation in order to destroy microorganisms. A radiation sterilization validation determines the appropriate radiation sterilization dose for a product that will be labeled as sterile. For more information please visit http://www.mobio.com

MO BIO Laboratories Inc., a privately held company located in the San Diego biotech corridor (Carlsbad, CA, USA), was founded in 1993 by Liz and Mark Brolaski. Initially a small business start-up, MO BIO has grown into a multi-million dollar operation with international production, research, and distribution. Today, MO BIO's growth and customer loyalty is challenging some of the world's leading molecular biology tool companies with innovative technologies and a commitment to value.