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As 1111

Manufactured by Aspen
Sourced in China

The AS-1111 is a high-precision laboratory instrument designed for conducting a variety of analytical and experimental tasks. It features advanced technical specifications, robust construction, and reliable performance. The core function of the AS-1111 is to provide precise measurements and data acquisition capabilities for scientific research and testing applications.

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3 protocols using as 1111

1

Immunofluorescence Staining of Cell Markers

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We fixed the cells by incubating in 4% PFA solution (AS1018, Aspen, Wuhan) for 30 min. Then, after blocking the fixed cells with 10% BSA (10735078001, Roche) at 37 °C for 30 min, they were incubated at 4 °C overnight with the following primary antibodies: anti-SERPINH1 (ab109117, Abcam); anti-E-cadherin (20874-1-AP, San Ying, Wuhan); and anti-N-cadherin (Abcam, Ab18203). Then, the cells were incubated with CY3- or FITC-conjugated goat anti–mouse or goat anti–rabbit IgG (AS-1111, Aspen, Wuhan) at 37 °C for 1 h. The cells were imaged and analyzed under a fluorescence microscope.
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2

Immunofluorescence Staining of Cell-Cell Junctions

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The cells were fixed with 4% paraformaldehyde (AS1018, Aspen, Wuhan) for 20 min. Then, the fixed cells were blocked with 10% bovine serum albumin (AS1018, Aspen, Wuhan) for 30 min, followed by incubation at 4°C overnight with the following primary antibodies: anti-E-cadherin (20874-1-AP, San Ying, Wuhan), anti-N-cadherin (Abcam, Ab18203), and anti-β-catenin (20874-1-AP, San Ying, Wuhan). After incubating the cells with CY3- or FITC-conjugated goat anti–mouse or goat anti–rabbit IgG (AS-1111, Aspen, Wuhan) secondary antibody at 37°C for 40 min, they were captured using fluorescence microscopy.
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3

Immunohistochemical Analysis of Uterine Markers

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After dewaxed and rehydrated with xylene and degraded ethanol, the tissue sections of uteri were labeled with primary antibodies against VEGF-A (1:50, sc-7269, Santa Cruz, USA), Angpt-1 (1:50, sc-6319, Santa Cruz, USA), or FGF-2 (1:100, sc-79, Santa Cruz, USA). The sections were incubated with Cy3-Goat anti Mouse (1:50, AS1111, ASPEN, China), Cy3-Donkey anti Goat (1:50, AS1113, ASPEN), and Cy3-Goat anti Rabbit (1:50, AS1109, ASPEN) secondary antibodies the next day. Then, these sections were observed under 100× magnifications.
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