E.i. Dupont De Nemours and Company

International N&h Denmark Aps

Raymond E Jackson

Richard C Ebersole

Rick Weizhang Ye

Abigail K Luckring

Michael P Perry

Edwin R Hendrickson

Robert K Kobos

Sharon Jo Keeler

Qiong Wang

Linda Jane DeCarolis

David J Regester

Laura Anne Bedzyk

Michael W Bostick

Stephen Varkey

Daniel R Demarco

John Thomas Gannon

Alexander D Kopatsis

Sheryl Wolstenholme

Miriam Lisa Ronchi

Julia Yager

Claus Lang

Victoria Vallejo Kelly

Amanda Chan

Daniel DeMarco

Provided herein, inter alia, are compositions of short chain fatty acid (SCFA)-producing microorganisms and methods of making and using the same to inhibit pathogenic bacterial populations in the gastrointestinal tracts of an animal and additionally promote improvement of one or more metrics in an animal, such as increased bodyweight gain, decreased feed conversion ratio (FCR), improved gut barrier integrity, reduced mortality, reduced pathogen infection, and reduced pathogen shedding in feces.

Compositions for gut health

Methods and materials for the detection of the foot and mouth disease virus (FMDV). The methods may utilize PCR amplification, with or without an internal positive control, and appropriate primer pairs. The reagents to perform these methods can be supplied as a kit and/or in tablet form.

Sequences diagnostic for foot and mouth disease

The present disclosure relates to isolation, identification and application ofstrain AL9:8 which grows on crude oil as the sole carbon source under denitrifying anaerobic conditionsstrain AL9:8 can be used alone or in concert with other microorganisms to improve oil recovery, bioremediation of oil or hydrocarbons in contaminated soil, ground water or bodies of water, such as lakes, rivers or oceans and/or applying to method for promoting oil pipeline maintenance, removing a build up hydrocarbon on the intersurfaces of the pipeline.

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Methods for the direct detection of diagnostic target RNA have been developed, which obviate the need for time consuming RNA purification and isolation procedures.

Method for the direct detection of diagnostic RNA

An apparatus is described for performing polymerase chain reaction (PCR) and capillary electrophoresis (CE) within a single, integrated and disposable device. Fluid enters the device via a sample charging port. From the sample charging port, the fluid travels through an inflow channel to the polymerase chain reaction chamber. This chamber is formed at a thin tab extension of a top portion of the device, and is generally defined by a cavity within the thin tab extension. After PCR is performed, the fluid leaves the polymerase chain reaction chamber through an outflow channel into a first sample well. A vent channel is connected to the first sample well for venting the first sample well to ambient atmosphere. The first sample well and a second sample well are in fluid communication by a sample channel. An electrophoresis separation channel is orthogonal to and intersects the sample channel, and has a first and second electrophoresis buffer well at each end. To perform electrophoresis, voltage is applied to the first and second sample well, and is then applied to the first and second electrophoresis buffer well.

Apparatus for integrated polymerase chain reaction and capillary electrophoresis

Growing community of inventors

Newark, DE, United States of America

Raymond E Jackson