Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human |
Applications: | WB, IF-Cell, FC |
Clonality: | Monoclonal |
Clone number: | JU33-05 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Protein A affinity purified. |
Molecular weight: | 52 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within Human NR0B1 aa 1-50 / 470. |
Positive control: | A549, Hela, SH-SY-5Y. |
Subcellular location: | Cytoplasm. Nucleus. |
Recommended Dilutions:
WB IF-Cell FC |
1:500 1:50-1:200 1:50-1:100 |
Uniprot #: | SwissProt: P51843 Human |
Alternative names: | AHC AHCH AHX DAX 1 DAX1 Dosage sensitive sex reversal DSS DSS AHC critical region on the X chromosome protein 1 DSS-AHC critical region on the X chromosome protein 1 GTD HHG Nr0b1 NR0B1_HUMAN NROB1 Nuclear hormone receptor Nuclear receptor 0B1 Nuclear receptor DAX 1 Nuclear receptor DAX-1 Nuclear receptor DAX1 Nuclear receptor subfamily 0 group B member 1 SRXY2 |
Fig1: Western blot analysis of NR0B1 on A549 cell lysate using anti-NR0B1 antibody at 1/500 dilution. | |
Fig2: ICC staining NR0B1 in A549 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. | |
Fig3: ICC staining NR0B1 in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. | |
Fig4: ICC staining NR0B1 in SH-SY-5Y cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. |
Fig5: Flow cytometric analysis of A549 cells with NR0B1 antibody at 1/100 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black). Alexa Fluor 488-conjugated goat anti-rabbit IgG was used as the secondary antibody. |