US2011318809A1PendingUtilityA1

Method of screening placental proteins responsible for pathophysiology of preeclampsia, and marker for early diagnosis and prediction of preeclampsia

Assignee: PARK WON SUNPriority: Jul 16, 2007Filed: Jun 7, 2011Published: Dec 29, 2011
Est. expiryJul 16, 2027(~1 yrs left)· nominal 20-yr term from priority
G01N 2550/00G01N 2800/368G01N 33/689G01N 33/561G01N 33/53G01N 33/6893G01N 33/543C12Q 1/37
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Claims

Abstract

The present invention relates to a method of screening placental proteins responsible for pathophysiology of preeclampsia, and a marker for early diagnosis and prediction of preeclampsia. In accordance with one aspect of the present invention, there is provided a method of screening placental proteins responsible for pathophysiology of preeclampsia by 2D E-proteomics analysis, comprising: isolating placental proteins from a placental tissue; separating the isolated proteins two-dimensionally through 2D electrophoresis; and comparing and analyzing the separated proteins based on scanned gel images and differences in the images between normal placental proteins and preeclamptic placental proteins, wherein the comparison and analysis of the placental proteins based on the scanned gel images and differences in the images are accomplished by selecting proteins with differences of 140% or more between two placentas.

Claims

exact text as granted — not AI-modified
1 - 4 . (canceled) 
     
     
         5 . A marker for early diagnosis and prediction of preeclampsia, comprising one or more proteins selected from the protein group consisting of chaperonin, ER-60 protease, isocitrate dehydrogenase 1, aldehyde reductase 1, fidaresta chain B bonded to human aldose reductase, voltage-dependent anion channel 1, nuclear chloride channel, cathepsin D chain H, phosphoglycerate mutase 1, endoplasmic reticulum protein, PSMA2 protein, glutathione S-transferase, Ig heavy chain v region, smooth muscle myosin alkali light chain, and fatty acid binding protein. 
     
     
         6 . The marker of  claim 5 , wherein the chaperonin, ER-60 protease, isocitrate dehydrogenase 1, aldehyde reductase 1, fidaresta chain B bonded to human aldose reductase, voltage-dependent anion channel 1, nuclear chloride channel, cathepsin D chain H, phosphoglycerate mutase 1, endoplasmic reticulum protein, PSMA2 protein, glutathione S-transferase, Ig heavy chain v region, smooth muscle myosin alkali light chain and fatty acid binding protein have the sequences of SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:15, SEQ ID NO:16, respectively.

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