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Each lot of this antibody is quality control tested by immunofluorescent staining with flow cytometric analysis. For immunofluorescent staining, the suggested use of this reagent is ≤0.25 µg per million cells in 100 µl volume. It is recommended that the reagent be titrated for optimal performance for each application.
COA:
Balb/c mouse splenocytes double stained with 330-AJ PE (lower panel ) or mouse IgG2a PE isotype control ( upper panel ) and anti-mouse CD45R/B220 (clone RA3-6B2) APC
Mouse Ly108, also known as SLAMF6 and NTB-A (NK cell, T cell, B cell antigen), is one of the members in The Signaling Lymphocytic Activation Molecule (SLAM) family of immune receptors. It is expressed on T cells, B cells, macrophages, dendritic cells, NK cells, and granulocytes. Homophilic interaction of Ly108 is involved in augmenting cytotoxicity of NK cells. Ly108 has been shown to function on NK cells by augmenting cytotoxicity. It was reported that Ly108 plays an important role in CD4+ T cell responses and innate immunity to bacteria and parasites. In a mouse with a targeted disruption of the Ly108 gene, CD4+ T cells and innate responses are defective. SLAM family of receptors has been implicated in the pathophysiology of autoimmunity. For instance, Ly108 is strongly linked to lupus susceptibility in mice. Ly108 may censor self-reactive B cells as a potential regulator of tolerance checkpoints, safeguarding against autoimmunity. Therefore, Ly108 serves as a regulator of both innate and adaptive immune responses.
Other Names:
SLAM family receptor, SLAMF6, TCOM, SF2000, KALI, SF-3, NTBA, NTB-A, NK-T-B antigen
Structure:
A glycoprotein of the signaling lymphocytic activation molecule family of cell surface receptor. It is a novel member of the CD2 subfamily of the Ig superfamily.
Distribution:
Expressed on T cells, B cells, macrophages, dendritic cells, NK cells, and granulocytes.
Function:
Play an important role in CD4+ T cell responses, innate immunity to bacteria and parasites, and NK cell function.
Ligand Receptor:
Ly108
Antigen References:
1. Howie D, et al. 2005. J. Immunology. 174 (10):5931 2 Kumar KR, et al. 2006. Science. 312(5780):1665 3. Zhong MC, et al. 2008. J. Biol. Chem. 283 (28):19255 4. Peck SR et al. 2000. Immunogenetics. 52:63
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This data display is provided for general comparisons between formats. Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors. If you need assistance with selecting the best format contact our expert technical support team.
Purified anti-mouse Ly108
Balb/c mouse splenocytes double stained with 330-AJ PE (lower panel ) or mouse IgG2a PE isotype control ( upper panel ) and anti-mouse CD45R/B220 (clone RA3-6B2) APC
Biotin anti-mouse Ly108
Balb/c mouse splenocytes double stained with 330-AJ biotin (lower panel) or mouse IgG2a biotin isotype control ( upper panel ) followed by Sav-PE and anti-mouse CD45R/B220 (clone RA3-6B2) APC
PE anti-mouse Ly108
Balb/c mouse splenocytes double stained with 330-AJ PE (lower panel ) or mouse IgG2a PE isotype control ( upper panel ) and anti-mouse CD45R/B220 (clone RA3-6B2) APC
Pacific Blue™ anti-mouse Ly108
C57BL/6 splenocytes stained with 330-AJ Pacific Blue™ and CD45R/B220 (RA3-6B2) PE
C57BL/6 splenocytes double stained with mouse IgG2a isotype control Pacific Blue™ and CD45R/B220 (RA3-6B2) PE
