Innovation

Method to Determine Increased Risk or Probability of Infertility

University of California System: University of California, Davis - UC Davis
posted on 06/08/2009

Determining whether an individual has an increased risk of infertility through the presence of a sequence variant to an highly expressed protein.

Suggested Uses

The use of this method as a diagnostic technique for determining an increased risk or probability of infertility.

Advantages

  • This method is effective in diagnosing individuals with increased risk of infertility;

  • Efficient and cost-effective as the biological sample can be evaluated by a broad range of detection methods, most ready available in biological laboratories and clinics;
  • May be less intrusive to the patient than the current marketed infertility tests as it requires only a biological sample;
  • Provides an alternative diagnostic tool for couples that have no other abnormalities in their reproductive evaluation; and
  • Can be used to diagnose individuals who suffer from unexplained infertility.

Innovation Details
 

Detailed Description

A sperm needs to maintain an immunoprotective shield until it arrives in the upper female reproductive tract and is competent to fertilize.  Researchers at the University of California, Davis have discovered a sequence variation of the gene that encodes the highly-expressed protein necessary for this immunoprotective shield.  The specific sequence variation significantly alters the structure and function of the protein, negatively impacting reproductive fitness, particularly sperm feunction and fertility.  The presence or lack of this sequence variation can be used to determine whether an individual has an increased risk or probability of infertility.

Determining if one has an increased risk of infertility is as simple as obtaining and analyzing a biological sample.  Methods of detection include a broad range of common biological laboratory techniques, including but not limited to, amplification reactions, hybridization, sequencing subsequences of the gene, restriction fragment length polymorphism, fluorescence resonance energy transfer, and usage of antibodies, ELISA, immunoprecipitation, Western blot, and protein array.  The presence of the sequence variation indicates an increased risk or probability of infertility.  Lack of the sequence variation indicates normal fertility.

File Number: 11444 


IP Protection

Copyright: ©2009-2010, The Regents of the University of California

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This innovation currently is not available for online licensing. Please contact Rajagopal Gururajan at University of California System: University of California, Davis - UC Davis for more information.

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Case Manager:

Rajagopal Gururajan Rajagopal Gururajan

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February 11, 2009

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