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Rabbit anti gs

Manufactured by Merck Group

Rabbit anti-GS is a primary antibody that binds to the glutamine synthetase (GS) protein. It is commonly used in various research and diagnostic applications that involve the detection and analysis of the GS protein.

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3 protocols using rabbit anti gs

1

Immunohistochemical Analysis of Retinal Protein

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Retinas were freshly dissected and immediately placed in 10% formalin overnight. Relief cuts were made and the retinas were embedded in 5% agarose. Using a vibratome, 150 μm transverse sections were cut and the sections were floated in PBS. After blocking in 1% bovine serum albumin, 0.5% Triton X-100, and 2% normal donkey serum for 2–3 hours, sections were incubated in primary antibody overnight at 4° C. After washing in PBS, secondary antibodies were applied at room temperature for 1 hour. Sections were again washed and then mounted for confocal microscopy (LSM710, Carl Zeiss). Antibodies were as follows: 3R10 mouse anti-RS17 (link) (gift of Professor Robert Molday, 1:5); rabbit anti-GS (Sigma, 1:1000); rabbit anti-synaptophysin (abcam, 1:1000).
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2

Immunofluorescence Staining of Lymphatic Markers

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The following antibodies were used: goat anti-LYVE-1 (polyclonal, R&D, AF2089), rat anti-PECAM-1 (clone 5D2.6 and IG5.1, provided by D. Vestweber, Max Planck Institute for Molecular Biomedicine Munster), rabbit anti-LYVE-1 (polyclonal, Reliatech), goat anti-LDLR (polyclonal, R&D, AF2255), rabbit anti-GS (polyclonal, Sigma-Aldrich, G2781), rabbit anti-CK19 (polyclonal, proteintech, 14965-1-AP), mouse anti-smooth muscle actin (SMA)-Cy3 (clone 1A4, Sigma), rat anti-Lyve-AlexaFluor594 (clone 223322, R&D), secondary antibodies coupled to AlexaFluor488, 568 and 647 (Invitrogen).
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3

Immunohistochemical Analysis of Retinal Protein

Check if the same lab product or an alternative is used in the 5 most similar protocols
Retinas were freshly dissected and immediately placed in 10% formalin overnight. Relief cuts were made and the retinas were embedded in 5% agarose. Using a vibratome, 150 μm transverse sections were cut and the sections were floated in PBS. After blocking in 1% bovine serum albumin, 0.5% Triton X-100, and 2% normal donkey serum for 2–3 hours, sections were incubated in primary antibody overnight at 4° C. After washing in PBS, secondary antibodies were applied at room temperature for 1 hour. Sections were again washed and then mounted for confocal microscopy (LSM710, Carl Zeiss). Antibodies were as follows: 3R10 mouse anti-RS17 (link) (gift of Professor Robert Molday, 1:5); rabbit anti-GS (Sigma, 1:1000); rabbit anti-synaptophysin (abcam, 1:1000).
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