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High-Throughput DNA Isolation

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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 operati
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
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