Fluorescence analyzing method, fluorescence analyzing apparatus and image detecting method
View Patent ↗A fluorescence analyzing method includes the steps of irradiating a board, to which oligonucleotide is fixed, with light for fluorescence measurement; focusing produced fluorescence to form an image; and detecting the fluorescence with a two-dimensional sensor. Here, the board is provided with plural regions to which the oligonucleotide is fixed, and the plural regions are spaced apart from one another on the board substantially equidistantly in the vertical and horizontal directions. A fluorescent image is detected in a condition where the following equation is satisfied: dd=ds×M/n where ds denotes the interval between the regions, M denotes the imaging magnification of an optical focusing/imaging system, dd denotes the pixel pitch of the two-dimensional sensor, and n denotes an integer (n=1, 2, 3, 4, 5).
1. A fluorescence analyzing method comprising the steps of:
irradiating a board, to which a plurality of oligonucleotides are fixed, with light for fluorescence measurement;
focusing produced fluorescence to form an image; and
detecting the fluorescence with a two-dimensional sensor, wherein:
the board is provided with multiple regions to each of which is fixed one of the plurality of oligonucleotides,
each region is spaced apart from an adjacent region on the board equidistantly in the vertical and horizontal directions,
the following equation is satisfied:
dd=ds×M/n
where ds denotes the distance between two adjacent regions, M denotes the imaging magnification of an optical focusing/imaging system, dd denotes the pixel pitch of the two-dimensional sensor, and n denotes an integer (n=1, 2, 3, 4, 5), and
ds is between 100 nm and 10000 nm.
2. A fluorescence analyzing method comprising the steps of:
irradiating a board, to which a plurality of oligonucleotides are fixed, with light for fluorescence measurement;
focusing produced fluorescence to form an image; and
detecting the fluorescence with a two-dimensional sensor, wherein:
the board is provided with multiple regions,
each region is spaced apart from an adjacent region equidistantly in the vertical and horizontal directions,
a single oligonucleotide molecule is fixed to at least a part of each of the multiple regions or identical oligonucleotide molecules are fixed to at least a part of each of the multiple regions,
the following equation is satisfied:
dd=ds×M/n
where ds denotes the distance between adjacent regions, M denotes the imaging magnification of an optical focusing/imaging system, dd denotes the pixel pitch of the two-dimensional sensor, and n denotes an integer (n=1, 2, 3, 4, 5), and
each region, has a diameter of 100 nm or less.
3. The fluorescence analyzing method according to any one of claims 1 and 2 , wherein n=2, 3.
4. The fluorescence analyzing method according to any one of claims 1 and 2 , wherein a film substance having an optical shield function is formed on a reaction region on the board, except for the multiple regions to which an oligonucleotide is fixed.
5. The fluorescence analyzing method according to claim 4 , wherein the film substance is a metal film.
6. The fluorescence analyzing method according to any one of claims 1 and 2 , wherein register markers are provided respectively to at least two positions on the board.
7. The fluorescence analyzing method according to any one of claims 1 and 2 , comprising means for adjusting the imaging magnification M to satisfy the equation, dd=ds×M/n.
8. The fluorescence analyzing method according to claim 7 , wherein the zooming function comprises means which automatically carries out the zooming according to a detection of the register markers.
9. A fluorescence analyzing method comprising the steps of:
irradiating a board, to which a plurality of oligonucleotides are fixed, with light for fluorescence measurement;
focusing produced fluorescence to form an image; and
detecting the fluorescence with a two-dimensional sensor, wherein:
the board is provided with multiple regions,
each region is spaced apart from an adjacent region equidistantly in the vertical and horizontal directions,
a single oligonucleotide molecule is fixed to each of at least a part of the multiple regions or identical oligonucleotide molecules are fixed to at least a part of each of the multiple regions,
the following equation is satisfied:
dd=ds×M/n
where ds denotes the distance between the adjacent regions, M denotes the imaging magnification of an optical focusing/imaging system, dd denotes the pixel pitch of the two-dimensional sensor, and n denotes an integer (n=1, 2, 3, 4, 5), and
ds is between 100 nm and 10000 nm inclusive.
10. A fluorescence analyzing method comprising the steps of:
irradiating a board, to which a plurality of oligonucleotides are fixed, with light for fluorescence measurement;
focusing produced fluorescence to form an image; and
detecting the fluorescence with a two-dimensional sensor, wherein:
the board is provided with multiple regions,
each region is spaced apart from an adjacent region equidistantly in the vertical and horizontal directions,
the following equation is satisfied:
dd=ds×M/n
where ds denotes the distance between adjacent regions, M denotes the imaging magnification of an optical focusing/imaging system, dd denotes the pixel pitch of the two-dimensional sensor, and n denotes an integer (n=1, 2, 3, 4, 5), and
has a diameter of 100 nm or less.