Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IHC-P |
Clonality: | Monoclonal |
Clone number: | JE58-81 |
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: 54 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within human Fukutin aa 312-461/461. |
Positive control: | A549 cell lysate, Mouse brain tissue lysate, Mouse liver tissue lysate, Rat cerebellum tissue lysate, Rat kidney tissue lysate, human liver tissue, human prostate carcinoma tissue, mouse liver tissue, rat kidney tissue. |
Subcellular location: | Golgi apparatus membrane, Nucleus, Cytoplasm. |
Recommended Dilutions:
WB IHC-P |
1:5,000 1:50-1:200 |
Uniprot #: | SwissProt: O75072 Human | Q8R507 Mouse Entrez Gene: 362520 Rat |
Alternative names: | CMD1X FCMD FCMD gene FKTN FKTN_HUMAN Fukutin Fukuyama type congenital muscular dystrophy protein Fukuyama-type congenital muscular dystrophy protein LGMD2M MDDGA4 MDDGB4 MDDGC4 MGC126857 MGC134944 MGC134945 MGC138243 OTTHUMP00000021841 patient fukutin |
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Fig1:
Western blot analysis of Fukutin on different lysates with Rabbit anti-Fukutin antibody (HA720031) at 1/5,000 dilution. Lane 1: A549 cell lysate (15 µg/Lane) Lane 2: Mouse brain tissue lysate (30 µg/Lane) Lane 3: Mouse liver tissue lysate (30 µg/Lane) Lane 4: Rat cerebellum tissue lysate (30 µg/Lane) Lane 5: Rat kidney tissue lysate (30 µg/Lane) Predicted band size: 54 kDa Observed band size: 50 kDa Exposure time: 3 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 (HA720031) at 1/5,000 dilution was used in primary antibody dilution (K1803) 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:
Immunohistochemical analysis of paraffin-embedded human liver tissue with Rabbit anti-Fukutin antibody (HA720031) at 1/200 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 (HA720031) at 1/200 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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Fig3: Immunohistochemical analysis of paraffin-embedded human prostate carcinoma tissue using anti-Fukutin antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA720031, 1/200) 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. |
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Fig4: Immunohistochemical analysis of paraffin-embedded mouse liver tissue using anti-Fukutin antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA720031, 1/200) 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. |
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Fig5: Immunohistochemical analysis of paraffin-embedded rat kidney tissue using anti-Fukutin antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA720031, 1/200) 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. |