Objective Lens Selection Guide
Objectives
Microscopy Objectives for Life Sciences, Dry Microscopy Objectives, Dry Microscopy Objectives, Oil Immersion Physiology Objectives, Water Dipping or Immersion Phase Contrast Objectives Long Working Distance Objectives Reflective Microscopy Objectives UV Focusing Objectives VIS and NIR Focusing Objectives
Scan Lenses and Tube Lenses
Scan Lenses F-Theta Scan Lenses Infinity-Corrected Tube Lenses

Did You Know?

Multiple optical elements, including the microscope objective, tube lens, and eyepieces, together define the magnification of a system. See the Magnification & FOV tab to learn more.

Click for Details
Example of a Dry Objective Design
(See Objective Tutorial Tab for More Information About Microscope Objective Types)

Thorlabs offers dry objectives made in house, as well as objectives from Olympus, Nikon, and Mitutoyo. Super apochromat, plan achromat, plan apochromat VIS⁺, plan apochromat, and plan fluorite (also called plan semi-apochromat or plan fluor) designs are available. For details about the differences between these types of objectives, please see the Objective Tutorial tab above.

When choosing a microscope objective, it is important to keep in mind that objectives are often designed to integrate with a particular manufacturer's microscopes. Before interchanging objectives, be sure to check the design tube lens focal length and the threading type of the objectives. A full list of specifications for each objective can be found in the Specs tab above. Please note that the performance of each objective may vary from the engraved specifications when integrated with components and systems from different manufacturers. See the Magnification and FOV tab for more information.

Our selection of dry objectives can be used in applications from microscopy to fiber coupling and includes options optimized for use at wavelengths from the UV to the NIR. For information on recommended applications for specific objectives, see below.

All objectives featured on this page are compatible with our microscope nosepiece modules for DIY Cerna^® systems, which accept RMS, M25 x 0.75, or M32 x 0.75 objective threading. Parfocal lengths can be matched by using our parfocal length extenders. The Olympus microscope objectives can be mounted directly to our fiber launch systems, or mounted into our 30 mm cage system using the CP42(/M) RMS-threaded cage plate, which is also post mountable. They can also be mounted to any of our multi-axis platforms or translation stages using an HCS013 RMS mount. Please note that the multi-axis platforms and translation stages need a 3 mm wide central keyway for the HCS013 RMS mount.

To use these objectives with a different thread standard, please see our microscope objective thread adapters.

• When Used with the Design Tube Lens Focal Length
• Specifications are for the TL1X-SAP objective with the wave plate attached unless otherwise noted.
• See the Objective Tutorial tab for more information about how this objective class is defined.
• Entrance pupil diameter (EP) is defined at the back aperture of the objective and calculated as EP=2*NA*EFL.
• The theoretical Rayleigh Resolution is determined by 0.61*λ/NA at λ = 550 nm; see the Resolution tab for details.

• When Used with the Design Tube Lens Focal Length
• See the Objective Tutorial tab for more information about how this objective class is defined.
• Entrance pupil diameter (EP) is defined at the back aperture of the objective and calculated as EP=2*NA*EFL.
• Without Cover Glass
• The theoretical Rayleigh Resolution is determined by 0.61*λ/NA at λ = 360 nm for the LMUL-10X-UVB and at λ = 550 nm for all other objectives; see the Resolution tab for details.

• When Used with the Design Tube Lens Focal Length
• Entrance pupil diameter (EP) is defined at the back aperture of the objective and calculated as EP=2*NA*EFL.
• The theoretical Rayleigh Resolution is determined by 0.61*λ/NA at λ = 360 nm for the LMUL-20X-UVB and at λ = 550 nm for all other objectives; see the Resolution tab for details.

• When Used with the Design Tube Lens Focal Length
• See the Objective Tutorial tab for more information about how this objective class is defined.
• Entrance pupil diameter (EP) is defined at the back aperture of the objective and calculated as EP=2*NA*EFL.
• The theoretical Rayleigh Resolution is determined by 0.61*λ/NA at λ = 360 nm for the LMUL-50X-UVB and at λ = 550 nm for all other objectives; see the Resolution tab for details.
• The axial color is optimized for the 436 to 850 nm range. Using this objective outside the optimized wavelength range will require refocusing.

• When Used with the Design Tube Lens Focal Length
• Entrance pupil diameter (EP) is defined at the back aperture of the objective and calculated as EP=2*NA*EFL.
• The theoretical Rayleigh Resolution is determined by 0.61*λ/NA at λ = 550 nm; see the Resolution tab for details.

Objective Tutorial

This tutorial describes features and markings of objectives and what they tell users about an objective's performance.

Objective Class and Aberration Correction

Objectives are commonly divided by their class. An objective's class creates a shorthand for users to know how the objective is corrected for imaging aberrations. There are two types of aberration corrections that are specified by objective class: field curvature and chromatic aberration.

Field curvature (or Petzval curvature) describes the case where an objective's plane of focus is a curved spherical surface. This aberration makes widefield imaging or laser scanning difficult, as the corners of an image will fall out of focus when focusing on the center. If an objective's class begins with "Plan", it will be corrected to have a flat plane of focus.

Images can also exhibit chromatic aberrations, where colors originating from one point are not focused to a single point. To strike a balance between an objective's performance and the complexity of its design, some objectives are corrected for these aberrations at a finite number of target wavelengths.

Five objective classes are shown in the table to the right; only three common objective classes are defined under the International Organization for Standards ISO 19012-2: Microscopes -- Designation of Microscope Objectives -- Chromatic Correction. Due to the need for better performance, we have added two additional classes that are not defined in the ISO classes.

Close

 

A cover glass, or coverslip, is a small, thin sheet of glass that can be placed on a wet sample to create a flat surface to image across.

The most common, a standard #1.5 cover glass, is designed to be 0.17 mm thick. Due to variance in the manufacturing process the actual thickness may be different. The correction collar present on select objectives is used to compensate for cover glasses of different thickness by adjusting the relative position of internal optical elements. Note that many objectives do not have a variable cover glass correction, in which case the objectives have no correction collar. For example, an objective could be designed for use with only a #1.5 cover glass. This collar may also be located near the bottom of the objective, instead of the top as shown in the diagram.

Click to Enlarge
The graph above shows the magnitude of spherical aberration versus the thickness of the coverslip used for 632.8 nm light. For the typical coverslip thickness of 0.17 mm, the spherical aberration caused by the coverslip does not exceed the diffraction-limited aberration for objectives with NA up to 0.40.

When viewing an image with a camera, the system magnification is the product of the objective and camera tube magnifications. When viewing an image with trinoculars, the system magnification is the product of the objective and eyepiece magnifications.

Magnification and Sample Area Calculations

Magnification

The magnification of a system is the multiplicative product of the magnification of each optical element in the system. Optical elements that produce magnification include objectives, camera tubes, and trinocular eyepieces, as shown in the drawing to the right. It is important to note that the magnification quoted in these products' specifications is usually only valid when all optical elements are made by the same manufacturer. If this is not the case, then the magnification of the system can still be calculated, but an effective objective magnification should be calculated first, as described below.

To adapt the examples shown here to your own microscope, please use our Magnification and FOV Calculator, which is available for download by clicking on the red button above. Note the calculator is an Excel spreadsheet that uses macros. In order to use the calculator, macros must be enabled. To enable macros, click the "Enable Content" button in the yellow message bar upon opening the file.

Example 1: Camera Magnification
When imaging a sample with a camera, the image is magnified by the objective and the camera tube. If using a 20X Nikon objective and a 0.75X Nikon camera tube, then the image at the camera has 20X × 0.75X = 15X magnification.

Example 2: Trinocular Magnification
When imaging a sample through trinoculars, the image is magnified by the objective and the eyepieces in the trinoculars. If using a 20X Nikon objective and Nikon trinoculars with 10X eyepieces, then the image at the eyepieces has 20X × 10X = 200X magnification. Note that the image at the eyepieces does not pass through the camera tube, as shown by the drawing to the right.

Using an Objective with a Microscope from a Different Manufacturer

Magnification is not a fundamental value: it is a derived value, calculated by assuming a specific tube lens focal length. Each microscope manufacturer has adopted a different focal length for their tube lens, as shown by the table to the right. Hence, when combining optical elements from different manufacturers, it is necessary to calculate an effective magnification for the objective, which is then used to calculate the magnification of the system.

The effective magnification of an objective is given by Equation 1:

(Eq. 1)

Here, the Design Magnification is the magnification printed on the objective, f_{Tube Lens in Microscope} is the focal length of the tube lens in the microscope you are using, and f_{Design Tube Lens of Objective} is the tube lens focal length that the objective manufacturer used to calculate the Design Magnification. These focal lengths are given by the table to the right.

Note that Leica, Mitutoyo, Nikon, and Thorlabs use the same tube lens focal length; if combining elements from any of these manufacturers, no conversion is needed. Once the effective objective magnification is calculated, the magnification of the system can be calculated as before.

Example 3: Trinocular Magnification (Different Manufacturers)
When imaging a sample through trinoculars, the image is magnified by the objective and the eyepieces in the trinoculars. This example will use a 20X Olympus objective and Nikon trinoculars with 10X eyepieces.

Following Equation 1 and the table to the right, we calculate the effective magnification of an Olympus objective in a Nikon microscope:

The effective magnification of the Olympus objective is 22.2X and the trinoculars have 10X eyepieces, so the image at the eyepieces has 22.2X × 10X = 222X magnification.

Sample Area When Imaged on a Camera

When imaging a sample with a camera, the dimensions of the sample area are determined by the dimensions of the camera sensor and the system magnification, as shown by Equation 2.

(Eq. 2)

The camera sensor dimensions can be obtained from the manufacturer, while the system magnification is the multiplicative product of the objective magnification and the camera tube magnification (see Example 1). If needed, the objective magnification can be adjusted as shown in Example 3.

As the magnification increases, the resolution improves, but the field of view also decreases. The dependence of the field of view on magnification is shown in the schematic to the right.

Example 4: Sample Area
The dimensions of the camera sensor in Thorlabs' previous-generation 1501M-USB Scientific Camera are 8.98 mm × 6.71 mm. If this camera is used with the Nikon objective and trinoculars from Example 1, which have a system magnification of 15X, then the image area is:

Sample Area Examples

The images of a mouse kidney below were all acquired using the same objective and the same camera. However, the camera tubes used were different. Read from left to right, they demonstrate that decreasing the camera tube magnification enlarges the field of view at the expense of the size of the details in the image.

Click to Enlarge
Acquired with 1X Camera Tube (Item # WFA4100)

Click to Enlarge
Acquired with 0.75X Camera Tube (Item # WFA4101)

Click to Enlarge
Acquired with 0.5X Camera Tube (Item # WFA4102)

Resolution Tutorial

An important parameter in many imaging applications is the resolution of the objective. This tutorial describes the different conventions used to define an objective's resolution. Thorlabs provides the theoretical Rayleigh resolution for all of the imaging objectives offered on our site; the other conventions are presented for informational purposes.

Resolution

The resolution of an objective refers to its ability to distinguish closely-spaced features of an object. This is often theoretically quantified by considering an object that consists of two point sources and asking at what minimum separation can these two point sources be resolved. When a point source is imaged, rather than appearing as a singular bright point, it will appear as a broadened intensity profile due to the effects of diffraction. This profile, known as an Airy disk, consists of an intense central peak with surrounding rings of much lesser intensity. The image produced by two point sources in proximity to one another will therefore consist of two overlapping Airy disk profiles, and the resolution of the objective is therefore determined by the minimum spacing at which the two profiles can be uniquely identified. There is no fundamental criterion for establishing what exactly it means for the two profiles to be resolved and, as such, there are a few criteria that are observed in practice. In microscopic imaging applications, the two most commonly used criteria are the Rayleigh and Abbe criteria. A third criterion, more common in astronomical applications, is the Sparrow criterion.

Rayleigh Criterion

The Rayleigh criterion states that two overlapping Airy disk profiles are resolved when the first intensity minimum of one profile coincides with the intensity maximum of the other profile [1]. It can be shown that the first intensity minimum occurs at a radius of 1.22λf/D from the central maximum, where λ is the wavelength of the light, f is the focal length of the objective, and D is the entrance pupil diameter. Thus, in terms of the numerical aperture (NA = 0.5*D/f), the Rayleigh resolution is:

r_R = 0.61λ/NA

An idealized image of two Airy disks separated by a distance equal to the Rayleigh resolution is shown in the figure to the left below; the illumination source has been assumed to be incoherent. A corresponding horizontal line cut across the intensity maxima is plotted to the right. The vertical dashed lines in the intensity profile show that the maximum of each individual Airy disk overlaps with the neighboring minimum. Between the two maxima, there is a local minimum which appears in the image as a gray region between the two white peaks.

Click to Enlarge
Left: Two point sources are considered resolved when separated by the Rayleigh resolution. The gray region between the two white peaks is clearly visible.
Above: The vertical dashed lines show how the maximum of each intensity profile overlaps with the first minimum of the other.

Thorlabs provides the theoretical Rayleigh resolution for all of the imaging objectives offered on our site in their individual product presentations.

Abbe Criterion

The Abbe theory describes image formation as a double process of diffraction [2]. Within this framework, if two features separated by a distance d are to be resolved, at a minimum both the zeroth and first orders of diffraction must be able to pass through the objective's aperture. Since the first order of diffraction appears at the angle: sin(θ₁) = λ/d, the minimum object separation, or equivalently the resolution of the objective, is given by d = λ/n*sin(α), where α is the angular semi-aperture of the objective and a factor of n has been inserted to account for the refractive index of the imaging medium. This result overestimates the actual limit by a factor of 2 because both first orders of diffraction are assumed to be accepted by the objective, when in fact only one of the first orders must pass through along with the zeroth order. Dividing the above result by a factor of 2 and using the definition of the numerical aperture (NA = n*sin(α)) gives the famous Abbe resolution limit:

r_A = 0.5λ/NA

In the image below, two Airy disks are shown separated by the Abbe resolution limit. Compared to the Rayleigh limit, the decrease in intensity at the origin is much harder to discern. The horizontal line cut to the right shows that the intensity decreases by only ≈2%.

Click to Enlarge
Left: Two point sources separated by the Abbe resolution limit. Though observable, the contrast between the maxima and central minimum is much weaker compared to the Rayleigh limit.
Above: The line cut shows the small intensity dip between the two maxima.

Sparrow Criterion

For point source separations corresponding to the Rayleigh and Abbe resolution criteria, the combined intensity profile has a local minimum located at the origin between the two maxima. In a sense, this feature is what allows the two point sources to be resolved. That is to say, if the sources' separation is further decreased beyond the Abbe resolution limit, the two individual maxima will merge into one central maximum and resolving the two individual contributions will no longer be possible. The Sparrow criterion posits that the resolution limit is reached when the crossover from a central minimum to a central maximum occurs.

At the Sparrow resolution limit, the center of the combined intensity profile is flat, which implies that the derivative with respect to position is zero at the origin. However, this first derivative at the origin is always zero, given that it is either a local minimum or maximum of the combined intensity profile (strictly speaking, this is only the case if the sources have equal intensities). Consider then, that because the Sparrow resolution limit occurs when the origin's intensity changes from a local minimum to a maximum, that the second derivative must be changing sign from positive to negative. The Sparrow criterion is thus a condition that is imposed upon the second derivative, namely that the resolution limit occurs when the second derivative is zero [3]. Applying this condition to the combined intensity profile of two Airy disks leads to the Sparrow resolution:

r_S = 0.47λ/NA

The image to the left below shows two Airy disks separated by the Sparrow resolution limit. As described above, the intensity is constant in the region between the two peaks and there is no intensity dip at the origin. In the line cut to the right, the constant intensity near the origin is confirmed.

Click to Enlarge
Left: Two Airy disk profiles separated by the Sparrow resolution limit. Note that, unlike the Rayleigh or Abbe limits, there is no decrease in intensity at the origin.
Above: At the Sparrow resolution limit, the combined intensity is a constant near the origin. The scale here has been normalized to 1.

References
[1] Eugene Hecht, "Optics," 4th Ed., Addison-Wesley (2002)
[2] S.G. Lipson, H. Lipson, and D.S. Tannhauser, "Optical Physics," 3rd Ed., Cambridge University Press (1995)
[3] C.M. Sparrow, "On Spectroscopic Resolving Power," Astrophys. J. 44, 76-87 (1916)