Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human |
Applications: | WB, IF-Cell, IHC-P |
Clonality: | Monoclonal |
Clone number: | JE62-21 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. 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: | Predicted band size: 30 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within human MRPS15 aa 158-257/257. |
Positive control: | HL-60 cell lysate, 293 cell lysate, HepG2 cell lysate, human tonsil tissue lysate, human breast carcinoma tissue, human small intestine tissue, Hela. |
Subcellular location: | Mitochondrion. |
Recommended Dilutions:
WB IF-Cell IHC-P |
1:500-1:2,000 1:50 1:100-1:400 |
Uniprot #: | SwissProt: P82914 Human |
Alternative names: | 28S ribosomal protein S15 28S ribosomal protein S15, mitochondrial [Precursor] DC37 FLJ11564 mitochondrial mitochondrial ribosomal protein S15 MPR S15 MRP-S15 MRPS15 RPMS15 RT15_HUMAN S15mt |
Fig1:
Western blot analysis of MRPS15 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (HA720106, 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: HL-60 cell lysate Lane 2: 293 cell lysate Lane 3: HepG2 cell lysate Lane 4: Human tonsil tissue lysate |
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Fig2: Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue using anti-MRPS15 antibody. 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 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA720106, 1/400) for 30 minutes 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. | |
Fig3: Immunohistochemical analysis of paraffin-embedded human small intestine tissue using anti-MRPS15 antibody. 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 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA720106, 1/100) for 30 minutes 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. |
Fig4:
Immunocytochemistry analysis of Hela cells labeling MRPS15 with Rabbit anti-MRPS15 antibody (HA720106) at 1/50 dilution. Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-MRPS15 antibody (HA720106) at 1/50 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) was used as the secondary antibody at 1/1,000 dilution. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (M1305-2, red) was stained at 1/200 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (Alexa Fluor® 647) were used as the secondary antibody at 1/1,000 dilution. |