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Rabbit anti cgrp

Manufactured by Immunostar
Sourced in United States

Rabbit anti-CGRP is a primary antibody that recognizes the calcitonin gene-related peptide (CGRP) protein. It is commonly used in research applications to detect and quantify the presence of CGRP in various biological samples.

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3 protocols using rabbit anti cgrp

1

Trigeminal Ganglia Immunohistochemistry

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Trigeminal ganglia were dissected, fixed in 4% paraformaldehyde in phosphate buffered saline (PBS) for 2 hours, washed in PBS overnight at 4° C, rinsed in PBS with 0.5% Triton X-100 (PBST), incubated with primary antibodies (chicken anti-GFP, Aves Labs, rabbit anti-CGRP, Immunostar) at 1:500 in blocking solution (PBST, 20% dimethylsolfoxide, 5% goat serum) for 48 hours, washed in PBST, incubated with secondary antibodies (anti-chicken 488, anti Rabbit-546, Invitrogen) at 1:500 in blocking solution overnight, and washed again in PBST.
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2

Immunohistochemical Profiling of Sensory Neurons

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Brain slices were frozen sectioned at 5 μm thickness and incubated with primary antibodies at 4°C overnight, followed by secondary antibody incubation at room temperature for 1 hour. Images were acquired with a Nikon AXR confocal microscope. Guinea pig anti-TRPV1 (Invitrogen, catalog PA129770, 1:1,000 dilution), rabbit anti-CGRP (Immunostar, catalog 24112, 1:500), donkey anti-mouse NeuN (Cell Signaling Technology, catalog 94403, 1:500 dilution), goat anti-rabbit Cy3 (Jackson Immunoresearch, catalog 111-165-003, 1:2,000 dilution), goat anti-mouse DyLight 405 (Jackson Immunoresearch, catalog 115-475-003, 1:250 dilution), and goat anti-guinea pig Cy3 (Jackson Immunoresearch, catalog 106-165-003, 1:2,000 dilution) were used.
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3

Immunofluorescence Staining Protocol for Spinal Cord and DRG

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Immunofluorescence staining was performed as previously described (Sun et al., 2017 (link)). Briefly, anesthetized mice were transcardially perfused with 0.9% saline followed by 4% paraformaldehyde (PFA) in 0.1 M phosphate buffer. Lumbar spinal cords (L3–L5) and DRGs were quickly removed and post-fixed in PFA overnight at 4°C. Then the tissues were transferred to 0.1 M phosphate buffer containing 30% sucrose at 4°C. The 40-μm-thick sections prepared by cryostat were washed 3 times and then blocked in 5% goat serum containing 0.3% Triton X-100 for 1 h at room temperature (RT). After incubation in the primary antibody overnight at 4°C, sections were incubated with the secondary antibodies at RT for 2 h and then were counterstained with DAPI. For primary antibodies, we used rabbit anti-CGRP (1:500, ImmunoStar, United States), Isolectin IB4 Conjugate (1:500, Invitrogen, United States), mouse anti-PKC-γ (1:200, Santa Cruz Biotechnology, United States), mouse mouse anti-PV (1:2000, Sigma-Aldrich, United States), rabbit anti-VGAT (1:500, Millipore, United States); For secondary antibodies, we used Alexa Fluor 488 goat anti-rabbit and Alexa Fluor 488 goat anti-mouse (1:500, Abways Technology, China). The Fluorescence images were captured using a laser scanning confocal microscope (Nikon A1 Confocal System, Japan).
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