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Natural Killer Cell Activation Pathway Bioinformatics

Disease and disorder research has been conducted in relation to the Natural Killer Cell Activation Pathway and Neoplasms, Malignant Neoplasms, Infective Disorder, Virus Diseases, Cytomegalovirus Infections. The study of the Natural Killer Cell Activation Pathway has been mentioned in research publications which can be found using our bioinformatics tool below. The Natural Killer Cell Activation Pathway has been researched in relation to Cell Activation, Immune Response, Secretion, Cell Proliferation, Cell Differentiation. The Natural Killer Cell Activation Pathway complements our catalog of research reagents including antibodies and ELISA kits against NK, NK1.1, CD69, CTLA4, DCX.

Natural Killer Cell Activation Bioinformatics Tool

Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Natural Killer Cell Activation below! For more information on how to use Laverne, please read the How to Guide.
Vizit™, under license from BioVista Inc.

Top Research Reagents

We have 2872 products for the study of the Natural Killer Cell Activation Pathway that can be applied to Flow Cytometry, Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.


Mouse Monoclonal
Species Human
Applications WB, Flow, CostimT

41 Publications

Rat Monoclonal
Species Mouse
Applications B/N, ELISA, Func

3 Publications
Western Blot: NOD2 Antibody (2D9) [NB100-524] - Western Blot Image of anti-NOD2 (2D9) Whole cell protein from THP-1 cells was separated on a 7.5% gel by SDS-PAGE, transferred to PVDF membrane and blocked in 5% non-fat milk in TBST. The membrane was probed with 2 ug/ml anti-NOD2 in 1% milk, and detected with an anti-mouse HRP secondary antibody using chemiluminescence.Immunocytochemistry/Immunofluorescence: NOD2 Antibody (2D9) [NB100-524] - A431 cells were fixed for 10 minutes using 10% formalin and then permeabilized for 5 minutes using 1X TBS + 0.5% Triton-X100. The cells were incubated with anti-NOD2 (2D9) NB100-524 at a 1:200 dilution overnight at 4C and detected with an anti-mouse Dylight 488 (Green) at a 1:500 dilution. Actin was counterstained with Phalloidin 568 (Red) at a 1:200 dilution. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 40X objective.

Mouse Monoclonal
Species Human, Mouse
Applications WB, ICC/IF, IHC

     1 Review

12 Publications
Western Blot: HLA DQA1 Antibody [NBP1-84550] - Lane 1: Marker [KDa] 250, 130, 100, 70, 55, 35, 25, 15, 10. Lane 2: Human cell line Daudi.Immunocytochemistry/Immunofluorescence: HLA DQA1 Antibody [NBP1-84550] - Staining of human cell line U-251MG shows positivity in cytoplasm.

Rabbit Polyclonal
Species Human
Applications WB, ICC/IF, IHC

Western Blot: CD161 Antibody (14F1F11) [NBP2-14845] - Western blot analysis of a partial CD161 recombinant protein using CD161 antibody at 1 ug/ml.

Mouse Monoclonal
Species Human
Applications WB

Western Blot: CD69 Antibody (15B5G2) [NBP2-25236] - analysis of CD69 in A) a partial recombinant protein and B) ThP1 lysate using CD69 antibody at 0.5 ug/ml. goat anti-mouse Ig HRP secondary antibody and PicoTect ECL substrate solution were used for this test.Immunohistochemistry-Paraffin: CD69 Antibody (15B5G2) [NBP2-25236] - Formalin-fixed, paraffin-embedded human tonsil stained with CD69 antibody (1 ug/ml), peroxidase-conjugate and DAB chromogen.

Mouse Monoclonal
Species Human
Applications WB, IHC, IHC-P

     1 Review

Western Blot: TRIF/TICAM1 Antibody [NB120-13810] - Analysis of TRIF in mouse spleen probed with TRIF antibody, in the A) presence and B) absence of immunizing peptide, at 1:1000.Immunocytochemistry/Immunofluorescence: TRIF/TICAM1 Antibody [NB120-13810] - TRIF antibody was tested in A431 cells with Dylight 488 (green). Nuclei and alpha-tubulin were counterstained with DAPI (blue) and Dylight 550 (red). Image objective 40x. An antibody dilution of 1:10 was used.

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications WB, Simple Western, ICC/IF

21 Publications
Western Blot: Doublecortin Antibody (3E1) [NBP1-92684] - Western blot of crude rat brain extract from a postnatal 3 day animal stained with NBP1-92684. Two bands at ~45kDa and ~35kDa show that NBP1-92684 binds to an epitope in the region of Doublecortin shared by Lis-A, and Lis-B, Lis-C and Lis-D, the C terminal 360 amino acids of Lis-A.Immunocytochemistry/Immunofluorescence: Doublecortin Antibody (3E1) [NBP1-92684] - Rat brain neural cultures stained with NBP1-92684 (green), a chicken polyclonal antibody to GFAP (NB300-213, red) and DNA (blue). The NBP1-92684 antibody reveals strong cytoplasmic staining in a population of small developing neurons. These cells are often found in small clumps as in these cultures, as in this example. Note that they are not positive for MAP2, which is characteristic of more mature neurons, and that the mature neuron shown is negative for NBP1-92684. This Doublecortin antibody is therefore an excellent marker of developing neuronal cells.

Mouse Monoclonal
Species Human, Mouse, Rat
Applications WB, ICC/IF

Western Blot: TLR3 Antibody (40C1285.6) [NBP2-24875] - analysis of TLR3 in lysates from A) untransfected 293, B) 293 cells transfected with human TLR3 cDNA, C) human intestine, D) placenta, E) heart and F) ovary using TLR3 antibody at 3 ug/ml. Goat anti-mouse HRP conjugate was used as secondary.Immunohistochemistry-Paraffin: TLR3 Antibody (40C1285.6) [NBP2-24875] - IHC analysis of a formalin fixed paraffin embedded tissue section of mouse intestine using TLR3 antibody (clone 40C1285.6) at 1:500 dilution with HRP-DAB detection and hematoxylin counterstaining. The representative image shows a punctate staining of the ER and endosomes in a subset of cells in Peyer's patches (organized lymphoid nodules) in the tested section.

Mouse Monoclonal
Species Human, Mouse, Canine
Applications WB, Flow, ICC/IF

61 Publications