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Biotin conjugated goat anti rabbit

Manufactured by Vector Laboratories
Sourced in United States

Biotin-conjugated goat anti-rabbit is a secondary antibody produced by Vector Laboratories. It is designed to detect and bind to rabbit primary antibodies, with biotin conjugated to the antibody structure.

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3 protocols using biotin conjugated goat anti rabbit

1

Immunohistochemical Analysis of Bone and Immune Markers

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Tissue was fixed with 4% paraformaldehyde, embedded in paraffin, and sectioned at a thickness of 4-6 μm. Following routine procedures including quenching of endogenous peroxidase and antigen retrieval, the sections were incubated with rabbit polyclonal antibodies against osteocalcin (1:100 dilution, ab93876; Abcam, Cambridge, UK), CD3 (1:100 dilution, 17A2; Biolegend, San Diego, CA, USA), or IFN-γ (1:100 dilution, bs-0480R; Bioss, Woburn, MA, USA). After washing, the sections were incubated for 30 min with biotin-conjugated goat anti-rabbit (1:500 dilution, BA-1000; Vector, Burlingame, CA, USA) or mouse IgG (1:500 dilution, BA-9200; Vector, Burlingame, CA, USA). Tissue sections were visualized using and avidin-horseradish peroxidase (HRP) and 3,3′-diaminobenzidine (DAB), followed by counterstaining with hematoxylin. Images were acquired under a microscope.
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2

Histological and Immunostaining Analysis of Mouse Brains

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Mouse brains were fixed in 4% paraformaldehyde in PBS at 4 °C for overnight, embedded in paraffin and sectioned at 7 μm in the coronal or sagittal planes. For histological analyses, sections were rehydrated and stained with hematoxylin and eosin. For immunostaining, after rehydration, sections were incubated in boiling citrate buffer (10 mM, pH6.0) for 30 min for antigen retrieval. After three washes with PBS, primary antibodies (Supplementary Methods) were incubated with 5% normal goat or donkey serum in PBS at 4 °C for overnight. Sections were then washed in PBS and incubated with the secondary antibodies. Primary antibodies information can be found in Supplementary Information. For secondary antibodies, Alexa Fluor 488-conjugated goat anti-mouse, anti-rabbit or anti-chicken, 647 conjugated goat anti-mouse (Invitrogen), Cy3-conjugated goat anti-mouse or anti-rabbit (Jackson ImmunoResearch), and biotin-conjugated goat anti-rabbit (Vector Labs) were used. Images were acquired using Axioplan 2 (Carl Zeiss) and confocal microscopes (TCS SP5 and SP8, Leica) and analysed with LAS AF (Leica) and Photoshop (Adobe).
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3

Immunohistochemical Analysis of TNF-α Expression

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Brain tissues were fixed in formalin and dehydrated by concentration gradient of ethanol and embedded into paraffin, and then were transversely cut into 5 μm sections, which were subjected to be stained with hematoxylin and eosin. The brain sections were dewaxed by Xylene, then hydrated, after heat antigen retrieval, the sections were labeled with anti-TNF-α antibody (R&D), biotin-conjugated goat anti-rabbit (KPL) as the secondary antibody labeled the primary antibody and combined with Elite AB (Vector), at last DAB were used for color development.
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