Rabbit Recombinant Monoclonal KLRF1 antibody - conjugated to PE. Suitable for Flow Cyt and reacts with Human samples.
pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: 98% PBS, 1% BSA
Flow Cyt | |
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Human | Tested |
Species | Dilution info | Notes |
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Species Human | Dilution info 1/2500 | Notes - |
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Functions as an activating receptor involved in immunosurveillance upon binding to various ligands displayed at the surface of myeloid cells. Upon interaction with CLEC2B ligand, stimulates NK-cell cytotoxicity and cytokine production leading to the cytolysis of malignant CLEC2B-expressing myeloid cells. Actviation of the common cytotoxicity pathway involves SRC and SYK kinases (PubMed:21149606).
CLEC5C, ML, KLRF1, Killer cell lectin-like receptor subfamily F member 1, Lectin-like receptor F1, Activating coreceptor NKp80, C-type lectin domain family 5 member C
Rabbit Recombinant Monoclonal KLRF1 antibody - conjugated to PE. Suitable for Flow Cyt and reacts with Human samples.
pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: 98% PBS, 1% BSA
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
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KLRF1 also known as CD314 or NKp80 is a receptor protein found primarily on natural killer (NK) cells with a significant mass of about 30 kDa. Researchers have identified its expression mainly in tissues rich in NK cells such as the spleen and peripheral blood. This receptor structurally belongs to the C-type lectin-like domain family and plays an important role in the immune response by binding to the CLEC2B ligand on target cells facilitating NK cell activation and cytotoxicity.
In immune surveillance and homeostasis KLRF1 acts as an important activating receptor on natural killer cells. It does not form a complex but works independently to control cellular immune responses by recognizing stress-induced ligands on target cells. Upon interaction with its ligand KLRF1 triggers a cascade of intracellular signals that promote cytotoxic activity and cytokine secretion contributing to the elimination of virally infected or transformed cells.
In the context of innate immune response signaling KLRF1 interacts with pathways involving NK cell-mediated cytotoxicity. KLRF1 engagement stimulates pathways similar to those activated by other receptors in the natural killer cell repertoire such as KLRK1 (NKG2D). These interactions play roles in maintaining balance within the immune system by modulating NK cell activity and ensuring efficient target cell elimination.
KLRF1 has implications in immune system-related conditions such as cancers and viral infections. Altered expression or function of KLRF1 may contribute to the escape of tumor cells from immune surveillance or decreased viral clearance. Associations with proteins like KLRD1 (CD94) in certain hematological malignancies suggest a role for KLRF1 in disease pathogenesis where NK cell dysfunction is present underlining its significance in developing therapeutic interventions.
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This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
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Flow cytometry staining of human peripheral blood mononuclear cells (PBMCs) with ab315145 (right) or Rabbit IgG (monoclonal) Phycoerythrin Isotype Control (PE Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab209478) (left). PBMCs were incubated for 30 min on ice in 1x PBS containing 10 µg/ml human IgG and 10 % normal goat serum to block FC receptors and non-specific protein-protein interaction followed by the antibody ab315145 or Rabbit IgG (monoclonal) Phycoerythrin Isotype Control (PE Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab209478) (1x 106in 100 µl at 0.2 µg/ml (1/2500)) for 30min on ice. The cells were simultaneously stained with CD56.
Acquisition of >30000 events were collected using a 50 mW Yellow/Green laser (561nm) and 585/42 bandpass filter. Events were gated on viable cells.
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