Product Type: | Rabbit polyclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IF-Cell, IHC-P, FC |
Clonality: | Polyclonal |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. 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: 45 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within human BMP2 aa 51-100. |
Positive control: | Caco-2 cell lysate, Saos-2 cell lysate, C2C12 cell lysate, C6 cell lysate, Hela, MCF-7, rat small intestine tissue, human breast cancer tissue, mouse small intestine tissue. |
Subcellular location: | Secreted. |
Recommended Dilutions:
WB IF-Cell IHC-P FC |
1:1,000 1:200 1:200 1:100-1:200 |
Uniprot #: | SwissProt: P12643 Human | P21274 Mouse | P49001 Rat |
Alternative names: | BDA2 BMP-2 BMP-2A Bmp2 BMP2_HUMAN BMP2A Bone morphogenetic protein 2 Bone morphogenetic protein 2A |
Fig1:
Western blot analysis of BMP2 on different lysates with Rabbit anti-BMP2 antibody (ER80602) at 1/1,000 dilution. Lane 1: Caco-2 cell lysate Lane 2: Saos-2 cell lysate Lane 3: C2C12 cell lysate Lane 4: C6 cell lysate Predicted band size: 45 kDa Observed band size: 38 kDa Exposure time: 2 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 (ER80602) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature. |
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Fig2: ICC staining BMP2 in Hela cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. DAPI was used to stain the cell nuclei (blue). | |
Fig3: ICC staining BMP2 in MCF-7 cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. DAPI was used to stain the cell nuclei (blue). |
Fig4: Immunohistochemical analysis of paraffin-embedded rat small intestine tissue using anti-BMP2 antibody. Counter stained with hematoxylin. | |
Fig5: Immunohistochemical analysis of paraffin-embedded human breast cancer tissue using anti-BMP2 antibody. Counter stained with hematoxylin. | |
Fig6: Immunohistochemical analysis of paraffin-embedded mouse small intestine tissue using anti-BMP2 antibody. Counter stained with hematoxylin. | |
Fig7: Flow cytometric analysis of Hela cells with BMP2 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. |