Pipette tip and method of use thereof

1. A method of isolating chromatin from a liquid sample, the method comprising passing the liquid sample through a pipette tip, such that the chromatin is retained on the rigid porous matrix in the pipette tip, the pipette tip having:

an open upper end adapted to engage a pipette;

an open lower end; and

a through passageway in fluid communication with the upper and lower ends;

the pipette tip being configured such that, in use, a liquid sample is capable of passing through the tip both by being drawn in through the lower end by the application of reduced pressure, and being expulsed out of the lower end by the application of increased pressure;

the pipette tip containing a rigid porous matrix on which a ligand is immobilized, the ligand being capable of binding to a protein associated with chromatin;

the rigid porous matrix being positioned within the pipette tip such that, in use, chromatin in a liquid sample passing through the pipette tip is retained by the rigid porous matrix;

wherein the rigid porous matrix comprises a sintered thermoplastic polymer, the matrix being functionalized at a surface after sintering, the functionalisation providing functional groups on the surface which facilitate the attachment of the ligand.

2. A method according to claim 1 , wherein the liquid sample is drawn multiple times through the lower end of the pipette tip by the application of reduced pressure and is expulsed multiple times out of the lower end of the pipette tip by the application of increased pressure.

3. A method according to claim 1 , wherein the drawing of the liquid sample through the lower end of the pipette tip is terminated at a time such that no air enters the rigid porous matrix.

4. A method according to claim 1 , wherein the ligand is an antibody.

5. A method according to claim 1 , wherein the ligand comprises an immunoglobulin, protein A or protein G.

6. A method of performing a chromatin immunoprecipitation assay, the method comprising the steps of:

(i) preparation of a liquid sample comprising chromatin to be analysed from cells;

(ii) immunoprecipitation of the chromatin in the liquid sample onto a rigid porous matrix to which a ligand is immobilised according to the method of claim 1 ;

(iii) DNA recovery from the chromatin immunoprecipitated in step (ii); and

(iv) DNA analysis.

7. A method of performing a chromatin immunoprecipitation assay, the method comprising the steps of:

(i) preparation of a liquid sample comprising chromatin to be analysed from cells;

(ii) passing the liquid sample through a pipette tip, thereby separating the chromatin from the liquid sample;

(iii) DNA recovery from the chromatin separated in step (ii); and

(iv) DNA analysis;

the pipette tip having:

an open upper end adapted to engage a pipette;

an open lower end; and

a through passageway in fluid communication with the upper and lower ends;

the pipette tip being configured such that, in use, a liquid sample is capable of passing through the tip both by being drawn in through the lower end by the application of reduced pressure, and being expulsed out of the lower end by the application of increased pressure;

the pipette tip containing a rigid porous matrix on which a ligand is immobilized, the ligand being capable of binding to a protein associated with chromatin;

the rigid porous matrix being positioned within the pipette tip such that, in use, chromatin in a liquid sample passing through the pipette tip is retained by the rigid porous matrix;

wherein the rigid porous matrix comprises a sintered thermoplastic polymer, the matrix being functionalized at a surface after sintering, the functionalisation providing functional groups on the surface which facilitate the attachment of the ligand.

8. A method according to claim 1 , wherein the rigid porous matrix is positioned within the pipette tip such that, in use, the proportion of liquid in the tip below the rigid porous matrix is less than 50% of the total volume of liquid in the tip.

9. A method according to claim 4 , wherein the rigid porous matrix is positioned within the pipette tip such that, in use, the proportion of liquid in the tip below the rigid porous matrix is less than 50% of the total volume of liquid in the tip.