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Affinity Purified anti-human interleukin-10 (IL-10)

 
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Contents: Affinity Purified anti-human interleukin-10 (IL-10)
Catalog Number: 14-7108
Formulation: Phosphate buffer pH 7.2,
150 mM NaCl, 0.09% NaN3
Storage Conditions: Store at 4°C.
Avoid repeated freeze/thaw cycles.
Clone: JES3-9D7
Isotype: Rat IgG1, κ

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14-7108-81 50 ug
14-7108-85 500 ug


   
data image 1
Human peripheral blood mononuclear cells were stimulated with PMA and ionomycin in the presence of Brefeldin A for 5 hours. The cells were surface stained with FITC anti-human CD4 (RPA-T4) and intracellularly stained with PE anti-human IL-10 (JES3-9D7).
Available Formats of This Product
Cat. No. Format Excite
(nm)
Emit
(nm)
Reported Applications
14-7108 Affinity Purified anti-human IL-10 (Interleukin-10, IL10) N/A N/A ELISA cap  ELISPOT cap  IHC(Paraffin) 
16-7108 Functional Grade* Purified anti-human IL-10 (Interleukin-10, IL10) N/A N/A ELISPOT cap  NU 
12-7108 PE anti-human IL-10 (Interleukin-10, IL10) 488 575 IC Flow 
51-7108 Alexa Fluor® 647 anti-human IL-10 (Interleukin-10, IL10) 633 668 IC Flow 
53-7108 Alexa Fluor® 488 anti-human IL-10 (Interleukin-10, IL10) 488 519 IC Flow 
57-7108 Pacific Blue® anti-human IL-10 (Interleukin-10, IL10) 402 421 IC Flow 
*Functional Grade™ (FG™) Purified: Azide-free, sterile-filtered, and endotoxin < 0.001 ng/µg  (unless otherwise noted).
*Functional Grade™ (FG™) Biotin: Azide-free, sterile-filtered, and endotoxin < 0.05 ng/µg.
  Purified: Contains azide, not sterile-filtered, and not endotoxin tested.
Flow Cytometry Product Notes:
Test Sizes: To accommodate multicolor flow cytometry, eBioscience is in the process of reducing test size volumes from 20 µl to 5 µl. Please check your antibody vial for the recommended test size.
Fluorochrome Replacements: eBioscience is in the process of replacing all Pacific Blue® and APC-Alexa Fluor® 750 conjugated products with eFluor™ 450 and APC-eFluor™ 780 conjugated products, respectively.

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Description


The JES3-9D7 monoclonal antibody reacts with human interleukin-10 (IL-10).


Applications Reported


For research use only, not for diagnostic or therapeutic use. The JES3-9D7 antibody has been reported for use in capture of human IL-10 by ELISA, intracellular flow cytometric analysis, and for neutralizing IL-10 bioactivity. (Use Functional Grade purified for functional studies cat.16-7108).


Applications Tested


The JES3-9D7 antibody has been tested as the capture antibody in a sandwich ELISA for analysis of human Interleukin-10 (IL-10) in combination with the biotin JES3-12G8 (13-7109) antibody for detection and recombinant human IL-10 (14-8109) as the standard. A suitable range of concentrations of this antibody for ELISA capture is 1-4 µg/ml. A standard curve consisting of doubling dilutions of the recombinant standard over the range of 1000 pg/ml - 8 pg/ml should be included in each ELISA plate.


References


Nowacki TM, Kuerten S, Zhang W, Shive CL, Kreher CR, Boehm BO, Lehmann PV, Tary-Lehmann M. Granzyme B production distinguishes recently activated CD8(+) memory cells from resting memory cells. Cell Immunol. 2007 May;247(1):36-48. (JES3-9D7, ELISPOT, PubMed)

Sendide K, Deghmane AE, Pechkovsky D, Av-Gay Y, Talal A, Hmama Z. Mycobacterium bovis BCG attenuates surface expression of mature class II molecules through IL-10-dependent inhibition of cathepsin S. J Immunol. 2005 Oct 15;175(8):5324-32. (JES3-9D7, FA, PubMed)

Martin M, Schifferle RE, Cuesta N, Vogel SN, Katz J, Michalek SM. Role of the phosphatidylinositol 3 kinase-Akt pathway in the regulation of IL-10 and IL-12 by Porphyromonas gingivalis lipopolysaccharide. J Immunol. 2003 Jul 15;171(2):717-25. (JES3-9D7, NU in vitro, PubMed)

Chandler SW, Rassekh CH, Rodman SM, Ducatman BS. Immunohistochemical localization of interleukin-10 in human oral and pharyngeal carcinomas. Laryngoscope. 2002 May;112(5):808-15. (JES3-9D7, IHC paraffin)

Abrams JS, Roncarolo MG, Yssel H, Andersson U, Gleich GJ, Silver JE. Strategies of anti-cytokine monoclonal antibody development: immunoassay of IL-10 and IL-5 in clinical samples.Immunol Rev. 1992 Jun;127:5-24.




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