LAMP-1 (lysosome-associated membrane glycoprotein 1; also P2B and CD107a) is a 120 kDa member of the LAMP family of proteins. It is a highly glycosylated type I transmembrane protein whose N-terminus projects either extracellularly or into the lumen of lysosomes. LAMP-1 may protect lysosomal membranes from enzymatic attack or mediate fusion of phagosomes with lysosomes. Mature mouse LAMP1 is 382 amino acids (aa) in length. It contains a 346 aa lumenal domain (aa 25‑370) and a 12 aa cytoplasmic region. Over aa 25‑370, mouse LAMP1 shares 82% and 62% aa identity with rat and human LAMP1, respectively.
Mouse LAMP-1/CD107a Lumenal Domain Antibody
R&D Systems | Catalog # AF4320
Scientific images may be resized, cropped, or adjusted for brightness or contrast for presentation purposes. These updates are limited to presentation and do not affect the underlying scientific interpretation of the data. Where available, additional source data may be provided upon request.
Key Product Details
Species Reactivity
Validated:
Cited:
Applications
Validated:
Cited:
Label
Antibody Source
Product Specifications
Immunogen
Leu25-Asn370
Accession # P11438
Specificity
Clonality
Host
Isotype
Scientific Data Images for Mouse LAMP-1/CD107a Lumenal Domain Antibody
Detection of Mouse LAMP‑1/CD107a by Western Blot.
Western blot shows lysates of mouse small intestine tissue and NIH-3T3 mouse embryonic fibroblast cell line. PVDF membrane was probed with 0.2 µg/mL of Goat Anti-Mouse LAMP-1/CD107a Lumenal Domain Antigen Affinity-purified Polyclonal Antibody (Catalog # AF4320) followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # HAF017). A specific band was detected for LAMP-1/CD107a at approximately 100-120 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.Detection of LAMP-1 in RAW 264.7 Mouse Cell Line by Flow Cytometry.
RAW 264.7 mouse monocyte/macrophage cell line was stained with Goat Anti-Mouse LAMP1/CD107a Lumenal Domain Antigen Affinity-purified Polyclonal Antibody (Catalog # AF4320, filled histogram) or control antibody (Catalog # AB-108-C, open histogram), followed by Allophycocyanin-conjugated Anti-Goat IgG Secondary Antibody (Catalog # F0108). To facilitate intracellular staining, cells were fixed with Flow Cytometry Fixation Buffer (Catalog # FC004) and permeabilized with Flow Cytometry Permeabilization/Wash Buffer I (Catalog # FC005). View our protocol for Staining Intracellular Molecules.LAMP1/CD107a in RAW 264.7 Mouse Cell Line.
LAMP1/CD107a was detected in immersion fixed RAW 264.7 mouse monocyte/macrophage cell line using Goat Anti-Mouse LAMP1/CD107a Lumenal Domain Antigen Affinity-purified Polyclonal Antibody (Catalog # AF4320) at 10 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Goat IgG Secondary Antibody (red; Catalog # NL001) and counterstained with DAPI (blue). Specific staining was localized to cytoplasm. View our protocol for Fluorescent ICC Staining of Cells on Coverslips.Detection of LAMP-1/CD107a by Immunocytochemistry/ Immunofluorescence
Liensinine induces ferritinophagic flux alterations by blocking autophagosome-lysosome fusion in alternatively activated macrophages.a Confocal microscopy images of the co-localization of ferritin (red) with LAMP1 (green), Scale bar = 100 µm (n = 3). b Confocal microscopy images of the co-localization of ferritin (red) with GFP-LC3 (green), Scale bar = 10 µm (n = 3). c Confocal microscopy images of immunostained GFP-LC-3 (green) and LAMP1 (red), Scale bar = 10 µm (n = 3). d Confocal microscopy images of LysoTracker Green (red) and GFP-LC3 (green), Scale bar = 10 µm (n = 3). Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/37353487), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of LAMP-1/CD107a by Immunocytochemistry/ Immunofluorescence
Liensinine induces ferritinophagic flux alterations by blocking autophagosome-lysosome fusion in alternatively activated macrophages.a Confocal microscopy images of the co-localization of ferritin (red) with LAMP1 (green), Scale bar = 100 µm (n = 3). b Confocal microscopy images of the co-localization of ferritin (red) with GFP-LC3 (green), Scale bar = 10 µm (n = 3). c Confocal microscopy images of immunostained GFP-LC-3 (green) and LAMP1 (red), Scale bar = 10 µm (n = 3). d Confocal microscopy images of LysoTracker Green (red) and GFP-LC3 (green), Scale bar = 10 µm (n = 3). Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/37353487), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Mouse LAMP-1/CD107a Lumenal Domain Antibody
CyTOF-ready
Immunocytochemistry
Sample: Immersion fixed RAW 264.7 mouse monocyte/macrophage cell line
Intracellular Staining by Flow Cytometry
Sample: RAW 264.7 mouse monocyte/macrophage cell line fixed with Flow Cytometry Fixation Buffer (Catalog # FC004) and permeabilized with Flow Cytometry Permeabilization/Wash Buffer I (Catalog # FC005)
Western Blot
Sample: Mouse small intestine tissue and NIH‑3T3 mouse embryonic fibroblast cell line
Reviewed Applications
Read 2 reviews rated 5 using AF4320 in the following applications:
Flow Cytometry Panel Builder
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Advanced Features
- Spectra Viewer - Custom analysis of spectra from multiple fluorochromes
- Spillover Popups - Visualize the spectra of individual fluorochromes
- Antigen Density Selector - Match fluorochrome brightness with antigen density
Formulation, Preparation, and Storage
Purification
Reconstitution
Reconstitute at 0.2 mg/mL in sterile PBS. For liquid material, refer to CoA for concentration.
Formulation
Shipping
Stability & Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Calculators
Background: LAMP-1/CD107a
Long Name
Alternate Names
Gene Symbol
UniProt
Additional LAMP-1/CD107a Products
Product Documents for Mouse LAMP-1/CD107a Lumenal Domain Antibody
Certificate of Analysis
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Product Specific Notices for Mouse LAMP-1/CD107a Lumenal Domain Antibody
For research use only
Citations for Mouse LAMP-1/CD107a Lumenal Domain Antibody
Customer Reviews for Mouse LAMP-1/CD107a Lumenal Domain Antibody (2)
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Customer Images
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Application: Western BlotSample Tested: Primary sorted Oligodendrocytes and Primary oligodendrocyte culturesSpecies: MouseVerified Customer | Posted 11/21/2019Clean band at predicted molecular weight, 10 ug of protein loaded per lane.Dilution of 0.2 mg/mL stock: 1:1000 Great antibody for each application tested so far on mouse tissue and cells: wb, IHC-Fr, ICC
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Application: Immunohistochemistry-FrozenSample Tested: Adult spinal cord and Primary culture of oligodendrocytesSpecies: MouseVerified Customer | Posted 11/21/2019P10 mouse ventral funiculus thoracic spinal cord stained with Lamp1 antibody (white) and Dapi.Dilution of 0.2 mg/mL stock: 1:40
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- 7-Amino Actinomycin D (7-AAD) Cell Viability Flow Cytometry Protocol
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- Extracellular Membrane Flow Cytometry Protocol
- Flow Cytometry Protocol for Cell Surface Markers
- Flow Cytometry Protocol for Staining Membrane Associated Proteins
- Flow Cytometry Staining Protocols
- Flow Cytometry Troubleshooting Guide
- ICC Cell Smear Protocol for Suspension Cells
- ICC Immunocytochemistry Protocol Videos
- ICC for Adherent Cells
- Immunocytochemistry (ICC) Protocol
- Immunocytochemistry Troubleshooting
- Immunofluorescence of Organoids Embedded in Cultrex Basement Membrane Extract
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Intracellular Flow Cytometry Protocol Using Alcohol (Methanol)
- Intracellular Flow Cytometry Protocol Using Detergents
- Intracellular Nuclear Staining Flow Cytometry Protocol Using Detergents
- Intracellular Staining Flow Cytometry Protocol Using Alcohol Permeabilization
- Intracellular Staining Flow Cytometry Protocol Using Detergents to Permeabilize Cells
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Propidium Iodide Cell Viability Flow Cytometry Protocol
- Protocol for Liperfluo
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Characterization of Human Th22 Cells
- Protocol for the Characterization of Human Th9 Cells
- Protocol for the Fluorescent ICC Staining of Cell Smears - Graphic
- Protocol for the Fluorescent ICC Staining of Cultured Cells on Coverslips - Graphic
- Protocol for the Preparation and Fluorescent ICC Staining of Cells on Coverslips
- Protocol for the Preparation and Fluorescent ICC Staining of Non-adherent Cells
- Protocol for the Preparation and Fluorescent ICC Staining of Stem Cells on Coverslips
- Protocol for the Preparation of a Cell Smear for Non-adherent Cell ICC - Graphic
- Protocol: Annexin V and PI Staining by Flow Cytometry
- Protocol: Annexin V and PI Staining for Apoptosis by Flow Cytometry
- R&D Systems Quality Control Western Blot Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Fluorokine Flow Cytometry Kits
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
- View all Protocols, Troubleshooting, Illustrated assays and Webinars