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Each lot of this antibody is quality control tested by ELISA assay. For ELISA capture applications, a concentration range of 0.5-2.0 μg/ml is recommended. To obtain a linear standard curve, serial dilutions of IL-6 recombinant protein ranging from 1000 to 8 pg/ml are recommended for each ELISA plate. It is recommended that the reagent be titrated for optimal performance for each application.
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Application Notes:
ELISA or ELISPOT Capture1-3,8: The purified MQ2-13A5 antibody is useful as the capture antibody in a sandwich ELISA or ELISPOT assay, when used in conjunction with the biotinylated MQ2-39C3 antibody (Cat. No. 501202/501203) as the detecting antibody. The LEAF™ purified antibody is suggested for ELISPOT capture. Neutralization1-3,6,7: The LEAF™ purified antibody (Endotoxin <0.1 EU/μg, Azide-Free, 0.2 μm sterile-filtered) is recommended for neutralization of human IL-6 bioactivity (Cat. No. 501110).
Application References:
1. Abrams, J., et al. 1992. Immunol. Rev. 127:5. 2. Abrams, J. 1995. Curr. Prot. Immunol.. John Wiley and Sons, New York. Unit 6.20. 3. Gaines Das, R., et al. 1993. J. Immunol. Meth. 160:147. 4. Enriquez, J., et al. 2002. Adv. Perit Dial. 18:177. 5. Andersson, U., et al. 1999. Detection and quantification of gene expression. New York:Springer-Verlag. 6. Zou, J-p., et al. 1999. J. Immunol. 162:4882. 7. Wyant, T. L., et al. 1999. Infect. Immun. 67:1338. 8. Lesmeister, M. J., et al. 2005. Reproductive Biology and Endocrinology 3:74. 9. Teresaka, Y., et al. 2010. Invest Opthalmol Vis Sci. 51:2441. PubMed
IL-6 is a potent lymphoid cell growth factor that stimulates the growth and survival of certain B cells and T cells. IL-6 plays a role in host defense, acute phase reactions, immune response, and hematopoiesis. IL-6 is expressed by T cells, B cells, monocytes, fibroblasts, hepatocytes, endothelial cells and keratinocytes. The MQ2-13A5 antibody can neutralize the bioactivity of natural or recombinant IL-6.
Other Names:
Interleukin-6, B cell stimulating factor-2 (BSF-2), Cytotoxic T cell differentiation factor (CDF), Hepatocyte stimulating factor (HSF), Hybridoma/plasmacytoma growth factor (HPGF)
Structure:
Neuropoietic cytokine family; 26 kD (Mammalian)
Regulation:
Upregulated by IL-1, TNF, PDGF, IFN-β, TNF-α, NGF, IL-17; downregulated by glucocorticoids IL-4, TGF-β
Cellular Sources:
T cells, B cells, macrophages, bone marrow stromal cells, fibroblasts, keratinocytes, mesangium, astrocytes, endothelial cells
Cellular Targets:
T cells, B cells, hepatocytes, cholinergic neurons
1. Fitzgerald, K., et al. Eds. 2001. The Cytokine FactsBook. Academic Press, San Diego. 2. Hirano, T. 1998. Intl. Rev. Immunol. 16:249. 3. Patterson, P. 1992. Curr. Opin. Neurobiol. 2:94. 4. Van Oers, M., et al. 1993. Ann. Hematology 66:219.
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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.
FITC anti-human IL-6
LPS-stimulated (6 hours) human peripheral blood monocytes surface stained with CD14 APC and intracellular stained with MQ2-13A5 FITC
LEAF™ Purified anti-human IL-6
PE anti-human IL-6
LPS-stimulated (6 hours) human peripheral blood monocytes were surface stained with CD14 FITC and then intracellular stained with MQ2-13A5 PE
Purified anti-human IL-6
APC anti-human IL-6
LPS-stimulated (6 hours) human peripheral blood monocytes surface stained with CD14 PE/Cy7 and intracellular stained with MQ2-13A5 APC