Table

Table 1. Basic optical components needed for single-molecule imaging

Microscopea Olympus IX70/IX71/IX81
Objectivesb
100X (1.45 NA) Olympus PlanApo 100X 1.45 NA, ∞/0.17
60X (1.45 NA) Olympus PlanApo 60X 1.45 NA, ∞/0.17 TIRFM
100X (1.65 NA) Olympus Apo 100X 1.65NA, ∞/0.15
100X (1.49 NA) Nikon Apo TIR 100X
CCD camerac Andor Technology iXonEM (DV887DCS-BV/DV887ECS-BV)
Andor Technology iXonEM+ (DV-897E-CS0)
Andor Technology iXonEM (DV860DCS-BV)
Lasers
Green laser (532 nm) CrystaLaser Diode-pumped solid-state laser (DPSS)
Red laser (633 nm) CrystaLaser / Melles Griot DPPS / Helium Neon (HeNe) (25-LHP-928-249)
Blue laser (488 nm) Melles Griot Argon-ion (35-LAS-450-120)
Mirrors, lenses, mounts, and posts
Broadband dielectric mirrors ThorLabs Inc. BB5-E02(1/2 in), BB1-E02(1 in), BB2-E02(2 in)
Kinematic mirror mounts ThorLabs Inc. KS05 (1/2 in), KS1(1 in), KS2(2 in)
Post holders ThorLabs Inc. PH6-ST/M - PH1-ST/M (ST = 6-1 in, M = 150-25 mm)
Posts ThorLabs Inc. TR6-TR075 (12.75 in) TR300/M - TR20/M (300-20 mm)
Manual linear translation stages Newport Corp. 423/433/443 series (requires actuators)
TIR focusing lens Thorlabs Inc. Plano-Convex lens, AR-coated
Beam expander Thorlabs Inc. i.e., 5X/10X (BE05M, BE10M)
Optical tabled
Sealed-hole optical table Newport Corp. RS4000
Pneumatic isolators Newport Corp. I-2000 LabLegs
Filters and dichroics: single color
Neutral density filters Thorlabs Inc. ND range 0.1-5 (NE01A - NE50A)
Excitation filters
532 nm Chroma Z532/10X (Z532BP)
633 nm Chroma Z633/10X (Z633BP)
488 nm Chroma Z488/10X (Z488BP)
Dichroics
532 nm; Cy3 Chroma Q565LP (41007)
633 nm, Cy5 Chroma Q660LP (41008)
488 nm, FITC/GFP Chroma Q505LP (41001)
Emission filters
532 ex, 570 em (Cy3) Chroma HQ585/70M
633 ex, 670 em (Cy5) Chroma HQ 690/90M
488 ex, 520 em (GFP, FITC) Chroma HQ525/50M
aThe Olympus microscope stage has a variable amount of drift. We often test up to three stages and choose the best one.
bOur standard objective is the 100X, NA = 1.45 objective, combined with a 1.5X (IX-71) or 1.6X (IX-70) magnifying lens in the microscope. With 16-μm CCD pixels (Andor, 512 × 512 camera), this gives 100-nm effective pixel size. Pixel sizes >120 μm are not recommended due to loss of resolution (Enderlein et al. 2006). We also use the 100X 1.65 NA, which requires special oil (n = 1.78, Model #9999902/4113/7, SPI Supplies) and special coverslips. Rarely, we use a 1.40 NA superapochromat, which is a very low chromatic aberration objective.
cEMCCD detectors--that is, cooled, back-thinned CCDs with an electron multiplication factor--are ideal detectors. Back-thinning allows for a quantum efficiency of ~90% (in the visible range). Thermoelectric cooling (to roughly -70ºC) reduces the noise due to CCD dark-current to virtually zero. Electron multiplication facilitates detection of even a small number of photons, which is enough to exceed the minimal background of the camera. The pixel size (16-24 μm) is generally reasonable, so that 160X magnification (100X of objective, plus 1.6X of internal microscope lens) provides an effective pixel size of 100-150 nm. This is reasonable, although the 24-μm pixel size generally requires an external lens in front of the camera.
dOur RS4000 optical tables are either 4 ft × 6 ft × 8 in or 4 ft × 10 ft × 8 in.

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  1. doi:10.1101/pdb.tab1ip45 Cold Spring Harb Protoc 2007: pdb.tab1ip45-

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