Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IF-Cell, IHC-P, IF-Tissue |
Clonality: | Monoclonal |
Clone number: | JE40-90 |
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: 17 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within Human TTC11 aa 1-125 / 152. |
Positive control: | Mouse spleen tissue lysate, mouse brain tissue lysate, rat spleen tissue lysate, rat brain tissue lysate, MCF-7, SH-SY-5Y, SK-Br-3, human kidney tissue, human small intestine tissue, human uterus tissue, mouse brain tissue, mouse colon tissue, rat brain tissue, rat colon tissue. |
Subcellular location: | Peroxisome. Mitochondrion. |
Recommended Dilutions:
WB IF-Cell IHC-P IF-Tissue |
1:500-1:2,000 1:50-1:200 1:1,000 1:200 |
Uniprot #: | SwissProt: Q9Y3D6 Human | Q9CQ92 Mouse | P84817 Rat |
Alternative names: | 2010003O14Rik CGI 135 CGI135 FIS 1 FIS1 Fis1 homolog FIS1, S. cerevisiae, homolog of FIS1_HUMAN Fission 1 (mitochondrial outer membrane) homolog (S. cerevisiae) Fission 1 (mitochondrial outer membrane) homolog (yeast) Fission 1 (mitochondrial outer membrane) homolog Fission 1 homolog H NH0132A01.6 hFis 1 hFis1 Mitochondrial fission 1 protein mitochondrial fission molecule Tetratricopeptide repeat domain 11 Tetratricopeptide repeat protein 11 TPR repeat protein 11 TTC 11 |
Fig1:
Western blot analysis of TTC11/FIS1 on different lysates with Rabbit anti-TTC11/FIS1 antibody (ET7109-17) at 1/1,000 dilution. Lane 1: Mouse spleen tissue lysate Lane 2: Mouse brain tissue lysate Lane 3: Rat spleen tissue lysate Lane 4: Rat brain tissue lysate Lysates/proteins at 40 µg/Lane. Predicted band size: 17 kDa Observed band size: 15 kDa Exposure time: 25 seconds; 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 (ET7109-17) 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: Western blot analysis of TTC11 on SK-Br-3 cell using anti-TTC11 antibody at 1/2,000 dilution. | |
Fig3: ICC staining TTC11 in MCF-7 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. |
Fig4: ICC staining TTC11 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: ICC staining TTC11 in SK-Br-3 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. | |
Fig6:
Immunohistochemical analysis of paraffin-embedded mouse brain tissue with Rabbit anti-TTC11/FIS1 antibody (ET7109-17) at 1/1,000 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 (ET7109-17) at 1/1,000 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. |
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Fig7:
Immunohistochemical analysis of paraffin-embedded mouse colon tissue with Rabbit anti-TTC11/FIS1 antibody (ET7109-17) at 1/1,000 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 (ET7109-17) at 1/1,000 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. |
Fig8:
Immunohistochemical analysis of paraffin-embedded rat brain tissue with Rabbit anti-TTC11/FIS1 antibody (ET7109-17) at 1/1,000 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 (ET7109-17) at 1/1,000 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. |
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Fig9:
Immunohistochemical analysis of paraffin-embedded rat colon tissue with Rabbit anti-TTC11/FIS1 antibody (ET7109-17) at 1/1,000 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 (ET7109-17) at 1/1,000 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. |