Adgre1 Rat Monoclonal Antibody [Clone ID: Cl:A3-1]

Specifications

Product Data
Clone Name	Cl:A3-1
Applications	FC, FN, IF, IHC, IP, R, WB
Recommend Dilution	Western Blot. Immunoprecipitation. Radioimmunoassays. Functional Assays. Flow Cytometry: Use 10 µl of 1/100-1/200 diluted antibody to label 106 cells in 100 µl. Immunohistochemistry on Resin Sections. Immunohistochemistry on Frozen Sections. Immunohistochemistry on Paraffin Sections: Requires pre-treatment prior to staining. Proteinase K is recommended for tissues fixed for less than 24 hours. Citrate buffer pH 6.0 is recommended for tissues fixed for more than 24 hours.
Reactivity	Mouse
Host	Rat
Clonality	Monoclonal
Immunogen	Thioglycollate stimulated peritoneal macrophages from C57/BL mice. Spleen cells from immunised HOB2 rats were fused with cells of the mouse NS1 myeloma cell line.
Specificity	This antibody recognises the F4/80 antigen. Clone CI:A3-1 has been reported to modulate cytokine levels released in response to Listeria monocytogenes.
Formulation	PBS, pH 7.4 State: Low Endotoxin State: Liquid purified IgG fraction Stabilizer: None Preservative: None
Concentration	lot specific
Purification	Affinity Chromatography on Protein G
Conjugation	Unconjugated
Storage Condition	Store the antibody undiluted at -20°C. Avoid repeated freezing and thawing.
Gene Name	adhesion G protein-coupled receptor E1
Database Link	Entrez Gene 13733 Mouse UniProt ID Q61549
Background	F4/80 is a 160 kD cell surface glycoprotein that is a member of the EGF-TM7 family of proteins which shares 68% overall amino acid identity with human EGF module-containing mucin-like hormone receptor 1 (EMR1). Expression of F4/80 is heterogeneous and is reported to vary during macrophage maturation and activation. The F4/80 antigen is expressed on a wide range of mature tissue macrophages including Kupffer cells, Langerhans, microglia, macrophages located in the gut lamina propria, peritoneal cavity, lung, thymus, bone marrow stroma and macrophages in the red pulp of the spleen. F4/80 expression has also been reported on a subpopulation of dendritic cells but is absent from macrophages located in T cell areas of the spleen and lymph node. The ligands and biological functions of the F4/80 antigen have not yet been determined but recent studies suggest a role for F4/80 in the generation of efferent CD8+ve regulatory T cells.
Synonyms	Emr1, Gpf480
Note	Endotoxin Level: < 0.01 Eu/µg Protocol: 1. Enzyme pre-treatment using Proteinase K (Recommended for tissues fixed for 24 hours in neutral buffered formalin, NBF): Reagents A. TE buffer (50 mM Tris base, 1 mM EDTA, pH 8.0) Tris Base, 6.10 g EDTA, 0.37 g Distilled water, 1000 ml Mix to dissolve. Adjust pH to 8.0 using concentrated HCl (10 M HCl). Store at room temperature. B. Proteinase K stock solution (20x, 400 μg/ml in TE buffer, pH 8.0) Proteinase K, 4 mg TE buffer, pH 8.0, (Reagent A) 10 ml Mix well. Store in aliquots at -20°C. C. Proteinase K working solution (1x, 20 μg/ml in TE buffer, pH 8.0) Proteinase K stock solution (20x), (Reagent B) 1 ml TE Buffer, pH 8.0, (Reagent A) 19 ml Mix well. Discard working solution after use. Method 1. Dewax paraffin sections and rehydrate using preferred procedure. 2. Cover sections completely with Proteinase K working solution and incubate for 3 minutes at RT. 3. Rinse sections with Phosphate Buffered Saline (PBS). 4. Proceed with serum blocking and preferred staining protocol. 2. Heat-mediated antigen retrieval using citrate buffer, pH 6.0 (Recommended for tissues fixed for 7 days or more in neutral buffered formalin, NBF): Reagent Citrate buffer (10 mM citric acid, pH 6.0) Citric acid (anhydrous), 1.92 g Distilled water, 1000 ml Mix to dissolve. Adjust pH to 6.0 with 1 M NaOH (be sure to mix well). Store this solution at RT for 3 months, or at 4°C for longer usage. Method 1. Dewax paraffin sections and rehydrate using preferred protocol. 2. Pre-heat sodium citrate buffer in a staining vessel to 95-100°C. 3. Immerse slides in the citrate buffer and incubate for 10 minutes at 95-100°C. Check the citrate buffer level, add more if necessary, and then incubate for a further 10 minutes at 95-100°C. 4. Allow sections to cool for 20 minutes. 5. Rinse sections with PBS. 6. Proceed with serum blocking and preferred staining protocol.
Reference Data

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