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SBIR TOPIC 229 - PHASE I, GENERATION and VALIDATION OF ERENNA ASSAYS FOR DETECTING

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: N43CM0700047
Agency Tracking Number: N43CM0700047
Amount: $749,084.00
Phase: Phase I
Program: SBIR
Solicitation Topic Code: N/A
Solicitation Number: N/A
Timeline
Solicitation Year: 2008
Award Year: 2008
Award Start Date (Proposal Award Date): N/A
Award End Date (Contract End Date): N/A
Small Business Information
SINGULEX, INC. 1650 Harbor Bay Parkway
Alameda, CA 94502
United States
DUNS: 946338688
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 Marianna Goldrick
 (512) 707-8993
 mgoldrick@biooscientific.com
Business Contact
Phone: (510) 995-9000
Email: s.agee@singulex.com
Research Institution
N/A
Abstract

The research will result in new kits for quantitative detection and monitoring of hypoxia inducible factor-1 alpha (Hif-1a), a promising cellular target protein for pharmacological intervention. During the Phase 1 project, monoclonal antibodies will be developed and used to create highly sensitive ELISA assays for Hif-1a. Mice immunized with peptides derived from Hif-1a will be used to produce hybridomas secreting anti-Hif antibodies. The prototype assay will be developed in Phase I and characterized using model systems of synthetic/recombinant targets and cultured cells, and SOPs will be created for production of all reagents and materials and for carrying out the assay. The prototype assay will be tested and reduced to practice using biological samples during Phase II. The ELISA assays that will be developed will be able to distinguish between the full-length active form of Hif-1a and the truncated form thought to act as a dominant negative regulator. The proposed ELISA assays will be used to evaluate candidate chemotherapeutic agents thought to affect Hif-1a. The successful development of the proposed assays will help to achieve the goals of the NCI Strategic Plan to support the more efficient evaluation and identification of targeted anti-tumor drugs.

* Information listed above is at the time of submission. *

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