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Anti trpv1 antibody

Manufactured by Alomone
Sourced in Israel

The Anti-TRPV1 antibody is a laboratory research tool used to detect and study the TRPV1 protein, which is a member of the transient receptor potential (TRP) ion channel family. The antibody can be used in various techniques, such as Western blotting, immunohistochemistry, and immunofluorescence, to identify and quantify the TRPV1 protein in biological samples.

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5 protocols using anti trpv1 antibody

1

TRPV1 Expression in Neuropathic Pain

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The rats were deeply anesthetized with pentobarbital (60 mg/kg, i.p.) on days 0, 7, or 14 after the start of PTX (4 mg/kg) treatment, and spinal cords were removed for Western blot analysis. Spinal cords were homogenized in cold 1× RIPA lysis buffer (Santa Cruz Biotechnology, Santa Cruz, CA, USA) containing phosphatase inhibitor cocktail (EDTA free) (Nacalai Tesque, Inc. Tokyo. Japan) and protease inhibitor cocktail (Nacalai Tesque). The homogenates were centrifuged at 4 °C for 30 min at 15,000× g, and the supernatants were collected. Spinal cord protein (30 μg) was separated by an SDS-polyacrylamide gel (7.5%) and transferred onto polyvinylidene difluoride membranes. Anti-TRPV1 antibody (1:200, Alomone Labs, Jerusalem, Israel) was used for Western blotting, with anti-β-actin (Sigma-Aldrich, 1:1000) used as the internal control. Horseradish peroxidase-labeled goat anti-rabbit immunoglobulin G (IgG) (Santa Cruz Biotechnology, 1:5000) was used as the secondary antibody. Specific bands were detected by enhanced chemiluminescence (ECL) with the ECLTM Prime Western Blotting Detection kit (GE Healthcare, Wauwatosa, WI, USA) using a luminescent image analyzer LAS4000 (Fuji Film, Japan). The intensities of immunoreactive bands were quantified using MultiGage Ver.3 software (Fuji Film, Tokyo, Japan).
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2

Spinal Cord TRPV1 Immunohistochemistry

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The rats were deeply anesthetized with pentobarbital (60 mg/kg, i.p.) on day 14 after the start of PTX (4 mg/kg) treatment, and spinal cords were prepared for immunohistochemistry. Rats were perfused transcardially with 20 mL of potassium-free phosphate-buffered saline (K+-free PBS; pH 7.4) followed by 50 mL 4% paraformaldehyde solution. The spinal cord (L4–6) was removed, post-fixed for 3 h, and cryoprotected overnight in 25% sucrose solution. The spinal cord was stored at −80 °C until use. The spinal cord sections were cut at 10 μm thickness, thaw-mounted on silane-coated glass slides, and air-dried overnight at room temperature. Spinal cord sections were incubated with excess blocking buffer containing 2% skim milk in 0.1% Triton X-100 in K+-free PBS, then subsequently reacted overnight at 4 °C with anti-TRPV1 antibody (Alomone Labs, 1:200) in 2% bovine serum albumin/0.1% Triton X-100 in K+-free PBS. The sections were then incubated in fluorescein isothiocyanate-conjugated anti-rabbit IgG (Sigma-Aldrich, 1:200) for 2 h at room temperature. All sections were treated with Permafluor (Thermo Shandon, Pittsburgh, PA, USA), cover-slipped, and evaluated with microscopy.
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3

Immunofluorescent Staining of FFPE Tissues

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Formalin fixed paraffin-embedded sections were de-paraffinized and rehydrated as follows: 100% Histo-Clear (National Diagnostics) for 5min, 100% ethanol for 1 min, 90% ethanol for 1 min, 70 % ethanol for 1 min and finally in PBS for 1 min. Before immunofluorescent staining, an antigen retrieval step was performed by incubating sections in 10 mM Sodium Citrate Buffer (10 mM Sodium Citrate Buffer, 0.05% Tween 20, pH 6.0) at 95° C for 1 hour. After cooling to room temperature for 30 min, slides were washed with PBS and blocked in blocking buffer (1X PBS, 10% goat serum, 0.5% TX- 100, 1% BSA) for 1 hour at room temperature. Sections were incubated with primary antibodies overnight at +4°C. β-III tubulin antibody (Abcam, cat# 78078) was used at a dilution of 1:250, while anti-TRPV1 antibody (Alomone labs, cat# ACC-030) was used at 1:100 dilution. Slides were washed three times in PBS for 5 min each and incubated in secondary antibodies and Hoescht (1:10000, Invitrogen) at room temperature. Slides were washed three times in PBS for 5 min each and coverslips were mounted by using Faramount Mounting media (Dako). Immunostained sections were analyzed on an Olympus FV1000 confocal microscope equipped with a laser scanning fluorescence and a 12 bit camera. Images were taken using a 60x oil PlanApo objective (with and without zoom feature).
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4

Immunofluorescence Analysis of TRPV1 and CGRP in Alveolar Bone

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TG were fixed in 4% paraformaldehyde for 24 h and embedded in paraffin. Tissue sections on slides were deparaffinized and incubated with anti-TRPV1 antibody (Alomone Labs, Jerusalem, Israel) and anti-CGRP antibody (Abcam) at 4 °C overnight. The slides were then incubated with Alexa Fluor 594 -conjugated anti-rabbit secondary antibody (Abcam) for TRPV1 and Alexa Fluor 488-conjugated anti-goat secondary antibody (Abcam) for CGRP at room temperature for 1 h. For histological analysis of alveolar bone tissues, decalcified and embedded sections were double-stained by anti-CGRP antibody and anti-PGP9.5 antibody (Novus Biologicals, Littleton, CO, USA) with appropriate Alexa Fluor-conjugated secondary antibodies. Slides were mounted with VECTASHIELD® HardSet™ Mounting Medium with DAPI (Vector laboratories, Burlingame, CA, USA) and analyzed by fluorescence microscopy (Keyence Corporation).
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5

Sperm Membrane Lipid Profiling Protocol

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Cholesterol, Epicholesterol (Epi-Chol), 2-hydroxypropyl-ß-cyclodextrin (CD), Superclean TM LC-Si SPE Tube 1 mL (Supleco), Filipin III from Streptomyces filipinensis, propidium iodide (PI) and Merocyanine 540 (MC540) were all purchased from Sigma Aldrich (Merck Group, Milan, Italy). Sperm washing medium (SWM) was purchased by Irvine Scientific (Santa Ana, CA, USA). Capsaicin was purchased from Millipore (Merck). Calcium OrangeTM AM was purchased from Thermo Fisher Scientific (Milan, Italy). Mouse monoclonal FITC-conjugated antihuman CD46 antibody was purchased from BD-Biosciences (Milan, Italy). Rabbit polyclonal anti-TRPV1 antibody was purchased from Alomone Labs (Jerusalem, Israel). FITC-conjugated antirabbit IgG, produced in goat, was purchased from Santa Cruz Biotechnology. All other reagents, solvents and salts were purchased from Fluka AG or Merck (Darmstadt, Germany).
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