US2006292703A1PendingUtilityA1

Biopolymer marker indicative of disease state having a molecular weight of 2753 daltons

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Assignee: JACKOWSKI GEORGEPriority: Apr 30, 2001Filed: Jul 13, 2006Published: Dec 28, 2006
Est. expiryApr 30, 2021(expired)· nominal 20-yr term from priority
Y10S436/811G01N 33/6893Y10T436/24
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Claims

Abstract

The instant invention involves the use of a combination of preparatory steps in conjunction with mass spectroscopy and time-of-flight detection procedures to maximize the diversity of biopolymers which are verifiable within a particular sample. The cohort of biopolymers verified within such a sample is then viewed with reference to their ability to evidence at least one particular disease state; thereby enabling a diagnostician to gain the ability to characterize either the presence or absence of said at least one disease state relative to recognition of the presence and/or the absence of said biopolymer.

Claims

exact text as granted — not AI-modified
1 . A method for screening for efficacy of disease process modulating agents for insulin resistance comprising: 
 (a) providing a sample of bodily fluid containing a biopolymer marker consisting of SEQ ID NO:1;    (b) adding a quantity of said agent sufficient to interact with said biopolymer marker consisting of SEQ ID NO:1; and    (c) determining the presence of an interaction between said agent and said biopolymer marker consisting of SEQ ID NO:1;    wherein said interaction is determinative of efficacy of said disease process modulating agent.    
     
     
         2 . A method for diagnosing insulin resistance comprising: 
 (a) providing a sample; and    (b) determining the presence of a biopolymer marker consisting of SEQ ID NO:1 in said sample;    wherein the presence of said biopolymer marker consisting of SEQ ID NO:1 is diagnostic for insulin resistance.    
     
     
         3 . The method of  claim 2 , wherein said sample is an unfractionated body fluid or a tissue sample.  
     
     
         4 . The method of  claim 2 , wherein said sample is selected from the group consisting of blood, blood products, urine, saliva, cerebrospinal fluid, and lymph.  
     
     
         5 . The method of  claim 2 , wherein said sample is from a human.

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