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CD158a/h (KIR2DL1/DS1)
Overview
The antibody is suitable for the identification and enumeration of CD158a (KIR2DL2)+ and CD158h (KIR2DS1)+ cells by flow cytometry and fluorescence microscopy. The family of killer immunoglobulin-like receptors (KIR) contributes to the regulation of NK cell–mediated cytotoxicity.
Details
Background information
Clone 11PB6, also referred to as EB6, recognizes CD158a (KIR2DL1) and CD158h (KIR2DS1), two members of the killer immunoglobulin-like receptor (KIR) family expressed on CD56dimCD16+ natural killer (NK) cells and CD8+ T cells.
Recent findings also showed reactivity of 11PB6 with KIR2DL3*005.1
CD158a (KIR2DL1) is involved in the transduction of an inhibitory signal whereas CD158h (KIR2DS1) is an activating receptor. The ligands of CD158a (KIR2DL1) are HLA-Cw4 and related molecules.
Clone Isotype
11PB6Mouse IgG1
 
Figure 1
Human PBMCs were stained with CD158a/h (KIR2DL1/DS1)-FITC (A), -PE (B), -APC (C), or VioBlue (D) and CD56-PE or -APC, respectively. Cells stained with CD158a/h (KIR2DL1/DS1)-Biotin were stained with Anti-Biotin-APC in addition (E). Cells were analyzed by flow cytometry using the MACSQuant® Analyzer.
A
B
C
D
E
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Products
CD158a/h (KIR2DL1/DS1)-FITC, human
- for 100 tests (1)
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130-092-811
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CD158a/h (KIR2DL1/DS1)-PE, human
- for 100 tests (1)
Download datasheet
130-092-684
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CD158a/h (KIR2DL1/DS1)-APC, human
- for 100 tests (1)
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130-092-685
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CD158a/h (KIR2DL1/DS1)-VioBlue, human
- for 100 tests (1)
Download datasheet
130-095-233
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CD158a/h (KIR2DL1/DS1)-Biotin, human
- for 100 tests (2)
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130-092-683
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CD158a/h (KIR2DL1/DS1) pure, human
- 100 µg in 1 mL
Download datasheet
130-092-682
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(1) One test corresponds to fluorescent labeling of up to 107 cells in a total volume of 100 µL.
(2) One test corresponds to labeling of up to 107 cells in a total volume of 100 µL.
Related products
MACS® Cell Separation Reagents for human NK cells
CD16 Antibodies
CD56 Antibodies
CD158e (KIR3DL1) Antibodies
CD158b (KIR2DL2/DL3) Antibodies
Anti-Biotin Antibodies
Mouse IgG1 - isotype control Antibodies
References
1. Falco M. et al. (2010) J. Immunol. 185: 433–441.
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