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>   home   >   Products   >   Primary Antibodies   >   Anti-Pig CD107a Antibody, clone 4E9/11    

Anti-Pig CD107a Antibody, clone 4E9/11 (FITC)

Mouse Anti-Pig Monoclonal Antibody

  • FC - Anti-Pig CD107a Antibody, clone 4E9/11 (FITC) ABD12240
    Published customer image:Mouse anti Pig CD107a antibody, clone 4E9/11 used for the detection of CD107a in porcine NK cells by flow cytometryImage caption:Analysis of degranulation capacity in NKp46-defined NK-cell subsets in blood. The cytolytic capacity of NKp46-defined NK-cell subsets (CD8&alpha;+NKp46-: blue, CD8&alpha;+NKp46+: green) isolated from blood was analysed after receptor triggering. Cells were stimulated with rhIL-2 and rpIL-15 overnight. Triggering of NK-receptors was performed by using monoclonal antibodies against NKp46, CD16 or a combination of both. Irrelevant isotype-matched antibody served as negative control. NK-cell receptor mediated degranulation was assessed by measuring the expression of CD107a on the cell surface by four-colour flow cytometry after one hour incubation. CD107a expression was measured on CD3- lymphocytes (not shown), followed by gating on the respective NKp46-defined NK subsets. (A) Numbers indicate the percentage of CD107a+ cells and the mean fluorescence intensity of CD107a within respective NKp46-gates. Results are representative of experiments with five different animals. (B) CD107a expression analyses of five animals analysed. The proportion of CD107a+ cells within the different NKp46-defined subsets is shown in the upper graphs. Percentage of CD107a+ NK cells was calculated by subtracting spontaneous degranulation observed in cultures stimulated with isotype-control antibodies from the frequency of CD107a+ cells in cultures stimulated with NKp46 and/or CD16 mAbs. The lower graphs show the mean fluorescence intensity of CD107a within the respective subsets. Mean values are represented by a black bar. Significant differences between the subsets are indicated (* = p < 0.05, ** = p < 0.01).From: Mair KH, M&uuml;llebner A, Essler SE, Duvigneau JC, Storset AK, Saalm&uuml;ller A, Gerner W. Porcine CD8&alpha;dim/-NKp46high NK cells are in a highly activated state. Vet Res. 2013 Mar 1;44:13.
  • FC - Anti-Pig CD107a Antibody, clone 4E9/11 (FITC) ABD12240
    Pig peripheral blood granulocytes stained with Mouse anti Pig CD107a followed by Goat anti Mouse IgG:FITC . Membrane permeabilisation was achieved with Leucoperm &trade;
Product Information
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
Reactivity Pig
Host Mouse
Clonality Monoclonal
Isotype IgG1
Clone Names 4E9/11
Additional Information
Purification Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant
Immunogen Porcine alveolar macrophages.
Shelf Life 18 months from date of despatch.
Target/Specificity Mouse anti-Pig CD107a, clone 4E9/11 recognizes porcine CD107a, a cell surface antigen, also known as lysosomal-associated membrane protein-1 or LAMP-1. CD107a is a type 1 single pass transmembrane glycoprotein expressed on macrophages and more weakly on monocytes and granulocytes.
Preservative & Stabilisers 0.09% Sodium Azide (NaN3); 1% Bovine Serum Albumin
Storage Store at +4℃ or -20℃.
PrecautionsAnti-Pig CD107a Antibody, clone 4E9/11 (FITC) is for research use only and not for use in diagnostic or therapeutic procedures.
Citations (0)

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1. Bullido, R. et al. (1997) Monoclonal antibodies specific for porcine monocytes/ macrophages: macrophage heterogeneity in the pig evidenced by the expression of surface antigens.
Tissue Antigens 49: 403-413. 2. Carrillo, A. et al. (2002) Isolation and characterization of immortalized porcine aortic endothelial cell lines.
Vet. Immunol. Immunopathol. 89: 91-98. 3. Domenech, N. et al. (2003) Identification of porcine macrophages with monoclonal antibodies in formalin-fixed, paraffin-embedded tissues.
Vet. Immunol. Immunopathol. 94: 77-81. 4. Sanchez-Torres, C. et al. (2003) Expression of porcine CD163 on monocytes/ macrophages correlates with permissiveness to African swine fever infection.
Arch. Virol. 148: 2307-2323. 5. Toka, F.N. et al. (2009) Natural killer cell dysfunction during acute infection with foot-and-mouth disease virus.
Clin Vaccine Immunol. 16: 1738-49. 6. Bullers, S.J. et al. (2014) The human tissue-biomaterial interface: a role for PPAR?-dependent glucocorticoid receptor activation in regulating the CD163+ M2 macrophage phenotype.
Tissue Eng Part A. 20: 2390-401. 7. Mair, K.H. et al. (2013) Porcine CD8αdim/-NKp46high NK cells are in a highly activated state.
Vet Res. 44: 13. 8. Cruz, J.L. et al. (2013) Alphacoronavirus Protein 7 Modulates Host Innate Immune Response
J Virol. 87: 9754-67. 9. van Hout, G.P. et al. (2015) Invasive surgery reduces infarct size and preserves cardiac function in a porcine model of myocardial infarction.
J Cell Mol Med. Aug 18. [Epub ahead of print] 10. Toka, F.N. et al. (2009) Activation of porcine natural killer cells and lysis of foot-and-mouth disease virus infected cells.
J Interferon Cytokine Res. 29 (3): 179-92.1. Piriou-Guzylack, L. (2008) Membrane markers of the immune cells in swine: an update.
Vet Res. 39: 54.

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