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Scientific Data Images for LRRC55 Antibody - BSA Free
Immunohistochemistry: LRRC55 Antibody - BSA Free [NBP1-81890]
Staining of human cerebellum shows moderate positivity in neuropil.Immunohistochemistry: LRRC55 Antibody - BSA Free [NBP1-81890]
Staining of human kidney shows strong membranous positivity in cells in glomeruli.Immunohistochemistry: LRRC55 Antibody - BSA Free [NBP1-81890]
Staining of human skeletal muscle shows no positivity in myocytes as expected.Immunohistochemistry: LRRC55 Antibody - BSA Free [NBP1-81890]
Staining of human small intestine shows moderate apical membrane positivity in glandular cells, as well as moderate immunoreactivity in the peripheral ganglion cells.Applications for LRRC55 Antibody - BSA Free
Immunohistochemistry
Immunohistochemistry-Paraffin
Reviewed Applications
Read 1 review rated 1 using NBP1-81890 in the following applications:
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Background: LRRC55
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Product Documents for LRRC55 Antibody - BSA Free
Certificate of Analysis
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Product Specific Notices for LRRC55 Antibody - BSA Free
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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Customer Reviews for LRRC55 Antibody - BSA Free (1)
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Customer Images
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Application: Immunohistochemistry-FrozenSample Tested: Adult mouse brain tissueSpecies: MouseVerified Customer | Posted 06/17/2021Lrrc55 is known highly expressed in the medial habenula (MHb) of mouse brain. However, the NBP1-81890-25ul Rabbit Polyclonal LRRC55 Antibody did not have any signal in the MHb.1. Wash in PBS 10min x 3 2. Incubation in 5% goat serum and 0.3% Triton X-100 for 2h at RT 3. 5% goat serum and 0.3% Triton X-100 4. Rabbit Polyclonal LRRC55 Antibody (1:50) 5. Goat anti-rabbit 488 6. PBS 10min x 3 7. DAPI 5min at RT 8. PBS 10min x 3 Mice were transcardially perfused with phosphate-buffered saline (PBS) followed by 4% paraformaldehyde. The brain was removed and post-fixed in 4% paraformaldehyde overnight at 4°C and dehydrated in 30% sucrose for 48 h. Coronal section (50 μm) containing the medial habenula were collected using a cryostat. The sections were rinsed 3 times with PBS for 10 min each and blocked with 5% goat serum and 0.3% Triton X-100 for 2 hours at room temperature and incubated for overnight at 4°C with following primary antibodies: anti-Lrrc55 (1:50, NBP1-81890-25UL). After 3 rinses with PBS for 10 min, secondary antibodies (1:1000, conjugated with Alexa 594) were incubated for 2 hours at room temperature. Then the sections were washed 3 times with PBS for 10 min each and stained with DAPI (1:10000 of 5 mg/mL). Images were acquired using a Zeiss 780 inverted confocal microscope.Bio-Techne ResponseThis review was submitted through the legacy Novus Innovators Program, reflecting a new species or application tested on a primary antibody.
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- Antigen Retrieval Protocol (PIER)
- Antigen Retrieval for Frozen Sections Protocol
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- Chromogenic IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Chromogenic Immunohistochemistry Staining of Frozen Tissue
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- Fluorescent IHC Staining of Frozen Tissue Protocol
- Graphic Protocol for Heat-induced Epitope Retrieval
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Graphic Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- IHC Sample Preparation (Frozen sections vs Paraffin)
- Immunofluorescent IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Immunohistochemistry Frozen Troubleshooting
- Immunohistochemistry Paraffin Troubleshooting
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Protocol for Heat-Induced Epitope Retrieval (HIER)
- Protocol for Making a 4% Formaldehyde Solution in PBS
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Preparation & Fixation of Cells on Coverslips
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections - Graphic
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections - Graphic
- Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Immunohistochemistry
- View all Protocols, Troubleshooting, Illustrated assays and Webinars