US2008108047A1PendingUtilityA1

Method for Separating Cells

43
Assignee: WOODSIDE STEVEN MPriority: Oct 1, 2001Filed: Nov 15, 2007Published: May 8, 2008
Est. expiryOct 1, 2021(expired)· nominal 20-yr term from priority
Inventors:Steven Woodside
Y10T436/25375Y10S435/803Y10S436/824G01N 35/00Y10T436/25
43
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

The present invention is related to a method for separating a first population of cells from a second population of cells in a sample by discontinuous density gradient separation using dense particles to target the first population of cells and a density separation medium (DSM) that is at least about 0.001 g/cm 3 higher than the density of the second population of cells.

Claims

exact text as granted — not AI-modified
1 - 27 . (canceled)  
     
     
         28 . A kit for separating a first population of cells from a second population of cells comprising one or more aliquots of a density separation medium having a density at least about 0.001 g/cm 3  greater than the mean density of the second population of cells, one or more aliquots of cell-specific targeting agents and one or more aliquots of dense particles.  
     
     
         29 . The kit according to  claim 28 , wherein the dense particles are red blood cells.  
     
     
         30 . The kit according to  claim 29 , wherein the cell-specific targeting agents are tetrameric antibody complexes that link the first population of cells to the red blood cells.  
     
     
         31 . The kit according to  claim 28 , wherein the dense particles are silica particles.  
     
     
         32 . The kit according to  claim 28 , wherein the cell-specific targeting agents are tetrameric antibody complexes that link the first population of cells to the dense particles.  
     
     
         33 . The kit according to  claim 28 , wherein the cell-specific targeting agent is an antibody or antibody cocktail that binds the first population of cells and the dense particles.  
     
     
         34 . The kit according to  claim 28  comprising one or more aliquots of a density separation medium having a density at least about 0.002 g/cm 3  greater than the mean density of the second population of cells.  
     
     
         35 . The kit according to  claim 28  comprising one or more aliquots of a density separation medium having a density at least about 0.004 g/cm 3  greater than the mean density of the second population of cells.  
     
     
         36 . A kit for separating a first population of cells from a second population of cells comprising one or more aliquots of a density separation medium having a density at least about 0.001 g/cm 3  greater than the mean density of the second population of cells, and one or more aliquots of dense particles coated with one or more cell-specific binding agents that bind the first population of cells.  
     
     
         37 . The kit according to  claim 36 , wherein the dense particles are red blood cells.  
     
     
         38 . The kit according to  claim 36 , wherein the dense particles are silica particles.  
     
     
         39 . The kit according to  claim 38 , wherein the dense particles are coated with one or more antibodies that bind the first population of cells.  
     
     
         40 . The kit according to  claim 39 , wherein the antibodies are tetrameric antibody complexes.  
     
     
         41 . The kit according to  claim 36  comprising one or more aliquots of a density separation medium having a density at least about 0.002 g/cm 3  greater than the mean density of the second population of cells.  
     
     
         42 . The kit according to  claim 36  comprising one or more aliquots of a density separation medium having a density at least about 0.004 g/cm 3  greater than the mean density of the second population of cells.  
     
     
         43 . The kit according  claim 28 , further comprising printed instructions.  
     
     
         44 . The kit according  claim 36 , further comprising printed instructions.

Cited by (0)

No later patents cite this yet.

References (0)

No backward citations on record.