CD161 Mouse Monoclonal Antibody [A8E1]
cat.: HA601063
Product Type: Mouse monoclonal IgG2b, primary antibodies
Species reactivity: Human
Applications: WB, IHC-P, FC
Clonality: Monoclonal
Clone number: A8E1
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1.1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 25 kDa
Isotype: IgG2b
Immunogen: Synthetic peptide within human CD161 aa 176-225.
Positive control: THP-1 cell lysate, HL-60 cell lysate, K-562 cell lysate, Jurkat cell lysate, human kidney tissue lysate, human kidney tissue, THP-1.
Subcellular location: Membrane
Recommended Dilutions:
  WB
  IHC-P
  FC

1:2,000
1:500
1:500-1:1,000
Uniprot #: SwissProt: Q12918 Human
Alternative names: C-type lectin domain family 5 member B CD161 CLEC5B HNKR-P1a Killer Cell Lectin like Receptor Subfamily B Member 1 Killer cell lectin-like receptor subfamily B member 1 KLRB1 KLRB1_HUMAN Natural killer cell surface protein P1A NKR NKR P1 NKR-P1A NKRP1 NKRP1A
Images
HA601063_1.jpg Fig1: Western blot analysis of CD161 on different lysates with Mouse anti-CD161 antibody (HA601063) at 1/2,000 dilution.

Lane 1: THP-1 cell lysate (20 µg/Lane)
Lane 2: HL-60 cell lysate (20 µg/Lane)
Lane 3: K-562 cell lysate (20 µg/Lane)
Lane 4: Jurkat cell lysate (20 µg/Lane)
Lane 5: Human kidney tissue lysate (40 µg/Lane)

Predicted band size: 25 kDa
Observed band size: 25 kDa

Exposure time: 3 minutes; ECL: K1801;

4-20% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA601063) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Anti-Mouse IgG for IP Nano-secondary antibody (NBI02H) at 1/5,000 dilution was used for 1 hour at room temperature.
HA601063_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human kidney tissue with Mouse anti-CD161 antibody (HA601063) at 1/500 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA601063) at 1/500 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
HA601063_3.jpg Fig3: Flow cytometric analysis of THP-1 cells labeling CD161.

Cells were washed twice with cold PBS and resuspend. Then stained with the primary antibody (HA601063, 1ug/ml) (red) compared with Mouse IgG1 Isotype Control (green). After incubation of the primary antibody at +4℃ for 30 minutes, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Mouse IgG Secondary antibody (HA1125) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.