Product Type: | Rabbit polyclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse |
Applications: | WB, IF-Cell, IHC-P, FC |
Clonality: | Polyclonal |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | 1*PBS (pH7.4), 0.2% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Immunogen affinity purified. |
Molecular weight: | Predicted band size: 21 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within C-terminal residues of PUMA. |
Positive control: | Hela cell lysate, Mouse kidney tissue lysate, SKOV-3, Hela, Lovo, human breast cancer tissue, mouse small intestine tissue, Jurkat. |
Subcellular location: | Mitochondrion. |
Recommended Dilutions:
WB IF-Cell IHC-P FC |
1:500-1:1,000 1:200 1:200 1:100 |
Uniprot #: | SwissProt: Q9BXH1 Human |
Alternative names: | BBC 3 Bbc3 BBC3_HUMAN BCL 2 binding component 3 Bcl-2-binding component 3 BCL2 binding component 3 JFY 1 JFY-1 JFY1 p53 up regulated modulator of apoptosis p53 up-regulated modulator of apoptosis p53 Upregulated Modulator of Apoptosis PUMA alpha PUMA/JFY1 |
Fig1:
Western blot analysis of PUMA on different cell lysate using anti- PUMA antibody at 1/1,000 dilution. Positive control: Lane 1: Hela cell lysate Lane 2: Mouse kidney tissue lysate |
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Fig2: ICC staining PUMA in SKOV-3 cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. | |
Fig3: ICC staining PUMA in Hela cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. | |
Fig4: ICC staining PUMA in Lovo cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. |
Fig5: Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue using anti-PUMA antibody. Counter stained with hematoxylin. | |
Fig6: Immunohistochemical analysis of paraffin-embedded mouse small intestine tissue using anti-PUMA antibody. Counter stained with hematoxylin. | |
Fig7: Flow cytometric analysis of Jurkat cells with PUMA antibody at 1/100 dilution (blue) compared with an unlabelled control (cells without incubation with primary antibody; red). Goat anti rabbit IgG (FITC) was used as the secondary antibody. |