Microarray based sample detection system
A microarray assembly for detection of a target molecule is disclosed. The microarray assemblies comprise an array chamber having a microarray located therein and features that facilitate liquid movement within the array chamber. Also disclosed are methods for making the microarray assembly using rollable films and methods for detecting microarray spots using an internal control fluorophore in the array spot.
1. A method of detecting a target molecule in a sample, comprising:
loading the sample in an microarray assembly, wherein the microarray assembly comprises:
a funnel-shaped array chamber with a sample inlet at a first end located at the start of the funnel shape, a sample outlet at a second end located at the end of the funnel shape, a top interior surface, a bottom interior surface, side walls and a microarray located on the bottom interior surface; and
a waste chamber that is in fluid communication with the outlet of the array chamber,
wherein the array chamber comprises a hydrophilic interior surface positioned to facilitate complete filling of the array chamber by a water-based fluid and the continuous flow of the fluid from the sample inlet to the sample outlet,
wherein the cross-sectional area at the first end of the array chamber is larger than the cross-sectional area at the second end of the array chamber, and wherein the array chamber is in the shape of a channel and wherein the cross- sectional area of the array chamber decreases in a continuous manner fiom the first end to the second end such that the capillary pressure continuously increase as the water-based fluid in the array chamber approached the waste chamber and therefore provides continuous wicking of the water-based fluid in the array chamber in the direction of the waste chamber;
incubating the sample in the array chamber to allow binding of the target molecule to the microarray; and
detecting the target molecule bound to the microarray.
2. The method of claim 1 , wherein the cross-sectional area of the array chamber at the first end is three-times larger than the cross-sectional area of the array chamber at the second.
3. The method of claim 1 , wherein the microarray comprises a plurality of array spots arranged in a single row extending from the first end to the second end of the array chamber.
4. The method of claim 1 , wherein the microarray comprises a plurality of parallel array strips that are perpendicular to the direction of sample flow in the array chamber.
5. The method of claim 1 , wherein the microarray is a gel spot microarray.
6. The method of claim 5 , wherein the gel spot microarray is an antibody array.
7. The method of claim 6 , wherein the gel spot microarray is a protein array.
8. The method of claim 6 , wherein gel spots of the gel spot microarray comprise protein probes covalently cross-linked to polymer backbone of the gel spots.
9. The method of claim 5 , wherein the microarray is an antibody array.
10. The method of claim 1 , wherein microarray assembly comprises a substrate layer, a cover layer and a spacer layer located between the substrate layer and the cover layer.
11. The method of claim 10 , wherein the spacer layer is a double-sided tape and wherein the array chamber is foil led within the spacer layer.
12. The method of claim 1 , wherein the microarray assembly comprises a substrate layer and a cover layer, wherein the substrate layer is an injection molded plastic with features that create walls of the array chamber and a pocket for the waste chamber.
13. The method of claim 12 , wherein the cover, layer is a hydrophilic film laminated to the substrate layer.
14. The method of claim 1 , further comprising amplifying the target molecule in the array chamber.
15. The method of claim 1 , wherein the target molecule is amplified by polymerase chain reaction.