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CD335/NKp46 Rabbit mAb (A25145)

Datasheet

Tested applications:WBIHC-PIF/ICCIPChIPChIP-seqRIPFCFC(Intra)ELISAMeDIPNucleotide ArrayDBFACSCoIPCUT&TagmeRIPInhibitionReactivity:Human

ABclonal:Western blot - CD335/NKp46 Rabbit mAb (A25145)

Western blot analysis of lysates from wild type (WT) and 293F cells transfected with CD335/NKp46 using CD335/NKp46 Rabbit mAb (A25145) at 1:1000 dilution incubated overnight at 4℃.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 20 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020)
.Exposure time: 30s.

ABclonal:Immunofluorescence - CD335/NKp46 Rabbit mAb (A25145)

Confocal imaging of 293F cells transfected with CD335/NKp46 using CD335/NKp46 Rabbit mAb (A25145, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). Objective: 100x.

ABclonal:Flow CytoMetry - CD335/NKp46 Rabbit mAb (A25145)

Flow cytometry: 1X10^6 293F cells (negative control, left) and 293F (Transfection, right) cells were surface-stained with CD335/NKp46 Rabbit mAb (A25145, 2 μg/mL, orange line) or ABflo® 647 Rabbit IgG isotype control (A22070, 5 μl/Test, blue line), followed by Alexa Fluor® 647 conjugated goat anti-rabbit pAb staining. Non-fluorescently stained cells were used as blank control (red line).

ABclonal:Flow CytoMetry - CD335/NKp46 Rabbit mAb (A25145)

Flow cytometry: 1X10^6 293F (Transfection) cells were surface-stained with ABflo® 647 Rabbit IgG isotype control (A22070, 5 μl/Test, left) or CD335/NKp46 Rabbit mAb (A25145, 2 μg/mL, right).

Overview

Product nameCD335/NKp46 Rabbit mAb
Catalog No.A25145
Host speciesRabbit
Purification methodAffinity purification
IsotypeIgG
CloneNo.ARC62449
The natural cytotoxic receptor (NCR) family includes NCR1 (NKp46/CD335), NCR2 (NKp44/CD336), and NCR3 (NKp30/CD337). They are type I single Transmembrane protein belonging to the immunoglobulin (Ig) superfamily. Various pathogenic and host coding molecules have been identified as ligands for NCR. They were initially discovered through their ability to induce cytotoxicity of natural killer (NK) cells to tumor cells in vitro, and animal models have shown that NCR plays a role in tumor monitoring, viral infection, and pregnancy in vivo. NCR1/NKP46 is considered a universal marker of NK cells, and recent studies have found that it is also expressed by other cells, such as the first group of natural lymphocytes (ILC1), a subgroup of the third group of ILC (NCR+ILC3), and γδ T cells. NCR1/NKp46 is also expressed in some malignant NK cells, natural killer T (NKT) cells and T-cell lymphoma, and is considered as a diagnostic marker and therapeutic target for them. The cross-linking of NCR1/NKp46 with antibodies can activate NK cells, which has been studied as a promising therapeutic pathway.
ImmunogenRecombinant fusion protein containing a sequence corresponding to amino acids 22-254 of human CD335/NKp46(NP_004820.2).
SequenceQQQTLPKPFIWAEPHFMVPKEKQVTICCQGNYGAVEYQLHFEGSLFAVDRPKPPERINKVKFYIPDMNSRMAGQYSCIYRVGELWSEPSNLLDLVVTEMYDTPTLSVHPGPEVISGEKVTFYCRLDTATSMFLLLKEGRSSHVQRGYGKVQAEFPLGPVTTAHRGTYRCFGSYNNHAWSFPSEPVKLLVTGDIENTSLAPEDPTFPADTWGTYLLTTETGLQKDHALWDHTAQ
Gene ID
Swiss Prot
SynonymsNCR1; CD335; LY94; NK-p46; NKP46; natural cytotoxicity triggering receptor 1
Calculated MW21kDa/22kDa/23kDa/32kDa/34kDa
Observed MW35-40kDa
ReactivityHuman
Tested applicationsWBIHC-PIF/ICCIPChIPChIP-seqRIPFCFC(Intra)ELISAMeDIPNucleotide ArrayDBFACSCoIPCUT&TagmeRIPInhibition
Recommended dilution
  • WB 1:500-1:1000
  • IF/ICC 1:50-1:200
  • FC 1:100 - 1:500
  • ELISA Recommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.
Storage bufferStore at -20℃. Avoid freeze / thaw cycles.
Buffer: PBS with 0.05% proclin300, 0.05% BSA, 50% glycerol, pH7.3.
Key applicationWestern blotting    Immunofluorescence    Flow Cytometry    
Positive samples293F cells transfected with CD335/NKp46
Cellular locationCell membrane, Single-pass type I membrane protein.

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ABclonal:Western blot - CD335/NKp46 Rabbit mAb (A25145)}

Western blot - CD335/NKp46 Rabbit mAb (A25145)

Western blot analysis of lysates from wild type (WT) and 293F cells transfected with CD335/NKp46 using CD335/NKp46 Rabbit mAb (A25145) at 1:1000 dilution incubated overnight at 4℃.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 20 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020)
.Exposure time: 30s.
ABclonal:Immunofluorescence - CD335/NKp46 Rabbit mAb (A25145)}

Immunofluorescence - CD335/NKp46 Rabbit mAb (A25145)

Confocal imaging of 293F cells transfected with CD335/NKp46 using CD335/NKp46 Rabbit mAb (A25145, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). Objective: 100x.
ABclonal:Flow CytoMetry - CD335/NKp46 Rabbit mAb (A25145)}

Flow CytoMetry - CD335/NKp46 Rabbit mAb (A25145)

Flow cytometry: 1X10^6 293F cells (negative control, left) and 293F (Transfection, right) cells were surface-stained with CD335/NKp46 Rabbit mAb (A25145, 2 μg/mL, orange line) or ABflo® 647 Rabbit IgG isotype control (A22070, 5 μl/Test, blue line), followed by Alexa Fluor® 647 conjugated goat anti-rabbit pAb staining. Non-fluorescently stained cells were used as blank control (red line).
ABclonal:Flow CytoMetry - CD335/NKp46 Rabbit mAb (A25145)}

Flow CytoMetry - CD335/NKp46 Rabbit mAb (A25145)

Flow cytometry: 1X10^6 293F (Transfection) cells were surface-stained with ABflo® 647 Rabbit IgG isotype control (A22070, 5 μl/Test, left) or CD335/NKp46 Rabbit mAb (A25145, 2 μg/mL, right).

* For research use only. Not for therapeutic or diagnostic purposes.

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