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Alpha plan apo 100x 1.46 oil objective lens

Manufactured by Zeiss

The Zeiss Alpha Plan-APO 100X/1.46 oil objective lens is a high-performance microscope objective designed for advanced imaging applications. It features a magnification of 100X and a numerical aperture of 1.46, providing high-resolution and detailed imaging capabilities. The lens is optimized for use with oil immersion techniques to enhance optical performance.

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5 protocols using alpha plan apo 100x 1.46 oil objective lens

1

High-resolution 3D Sperm Visualization

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Immunostained mouse epididymal sperm and elongated spermatids (steps 13-16) in dissociated testicular cells were prepared as described in Immunocytochemistry. 3D structural illumination microscopy (SIM) imaging was performed with Zeiss LSM710 Elyra P1 using alpha Plan-APO 100X/1.46 oil objective lens (Carl Zeiss). z stack images was acquired with 100 or 200 nm intervals and each section was taken using images were taken using 5 grid rotations with a 51 nm SIM grating period and a laser at 561 nm wavelength. Raw images were processed and rendered using Zen 2012 SP2 software (Carl Zeiss).
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2

Immunofluorescence Analysis of Sperm Proteins

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Sperm were washed in PBS twice, attached on glass coverslips, and fixed with 4% paraformaldehyde (PFA) in PBS at room temperature (RT) for 10–15 minutes. Fixed samples were permeabilized using 0.1% Triton X-100 in PBS at RT for 10 minutes and blocked with 10% normal goat serum in PBS at RT for 1 hr. Cells were stained with DHCR24 (1:500, Cell Signaling Technology) or IZUMO (1:250, Bio-Academia) antibody in 10% goat serum in PBS at 4°C overnight. After washing in PBS, the samples were incubated with secondary antibody (1:1,000) in 10% goat serum in PBS at RT for 1 hr. Hoechst was used to counterstain nucleus. Immunostained samples were mounted with Prolong gold (Invitrogen) and cured for 24 h, or with VectaShield (Vector laboratories), followed by confocal imaging with Zeiss LSM710 using Plan-Apochrombat 63X/1.40 or alpha Plan-APO 100X/1.46 oil objective lens (Carl Zeiss).
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3

Immunostaining of Mouse and Human Sperm

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Mouse and human sperm were washed in PBS twice, attached on the glass coverslips, and fixed with 4% paraformaldehyde (PFA) in PBS at room temperature (RT) for 10 minutes (mouse) or at 4°C for 1 hr (human). Fixed samples were permeabilized using 0.1% Triton X-100 in PBS at RT for 10 minutes, washed in PBS, and blocked with 10% goat serum in PBS at RT for 1 hr. Cells were stained with anti-mouse EFCAB9 (20 μg/ml), CatSper1 (10 μg/ml), or CatSperζ (20 μg/ml) in PBS supplemented with 10% goat serum at 4°C overnight. After washing in PBS, the samples were incubated with goat anti-rabbit Alexa647 or Alexa555-plus (Invitrogen, 1:1,000) in 10% goat serum in PBS at RT for 1 hr. Immunostained samples were mounted with Prolong gold (Invitrogen) and cured for 24 hr, followed by imaging with Zeiss LSM710 Elyra P1 using Plan-Apochrombat 63X/1.40 and alpha Plan-APO 100X/1.46 oil objective lens (Carl Zeiss). Hoechst dye was used to counterstain nucleus for sperm head.
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4

High-resolution 3D Sperm Visualization

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Immunostained mouse epididymal sperm and elongated spermatids (steps 13-16) in dissociated testicular cells were prepared as described in Immunocytochemistry. 3D structural illumination microscopy (SIM) imaging was performed with Zeiss LSM710 Elyra P1 using alpha Plan-APO 100X/1.46 oil objective lens (Carl Zeiss). z stack images was acquired with 100 or 200 nm intervals and each section was taken using images were taken using 5 grid rotations with a 51 nm SIM grating period and a laser at 561 nm wavelength. Raw images were processed and rendered using Zen 2012 SP2 software (Carl Zeiss).
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5

Immunolabeling of Mouse and Human Sperm

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Mouse and human sperm were washed in PBS twice, attached on the glass coverslips, and fixed with 4% paraformaldehyde (PFA) in PBS at room temperature (RT) for 10 min (mouse) or at 4°C for 1 hr (human). Fixed samples were permeabilized using 0.1% Triton X-100 in PBS at RT for 10 min, washed in PBS, and blocked with 10% goat serum in PBS at RT for 1 hr. Cells were stained with antibody in PBS supplemented with 10% goat serum at 4°C overnight. After washing in PBS, the samples were incubated with goat anti-rabbit Alexa 647 or Alexa 555-plus (Invitrogen, 1:1,000) in 10% goat serum in PBS at RT for 1 hr. Hoechst was used to counterstain nucleus for sperm head. For BODIPY-N-ethylmaleimide labeling, reduced thiols within proteins were alkylated with BODIPY FL maleimide (final concentration of 10 nM, ThermoFisher) for 30 min in the dark after permeabilization. The sample was then quenched by the addition of 500 mM 2mercaptoethanol for 30 min in the dark, followed by 3 times washing in PBS. For ThiolTracker (ThermoFisher) labeling, fixed sperm were stained with 20 μM dye, followed by 3 times washing in PBS. Stained sperm samples were mounted with Prolong gold (Invitrogen) and cured for 24 hr, followed by imaging with Zeiss LSM710 Elyra P1 using Plan-Apochrombat 63X/1.40 or alpha Plan-APO 100X/1.46 oil objective lens (Carl Zeiss).
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