Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IHC-P, IF-Cell |
Clonality: | Monoclonal |
Clone number: | JB49-18 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. 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: 44 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide of C terminal Human SNF5. |
Positive control: | Daudi cell lysate, PC-12 cell lysate, Human lung tissue lysate, Mouse brain tissue lysate, Rat brain tissue lysate, NIH/3T3, human kidney tissue, mouse large intestine tissue, rat kidney tissue, mouse colon tissue. |
Subcellular location: | Nucleus. |
Recommended Dilutions:
WB IHC-P IF-Cell |
1:1,000 1:50-1:500 1:100 |
Uniprot #: | SwissProt: Q12824 Human | Q9Z0H3 Mouse | Q4KLI0 Rat |
Alternative names: | BAF47 BRG1-associated factor 47 hSNF5 INI1 Integrase interactor 1 protein Malignant rhabdoid tumor suppressor RDT RTPS1 Sfh1p SMARCB1 SNF5 homolog SNF5_HUMAN SNF5L1 Snr1 Sucrose nonfermenting yeast homolog like 1 SWI/SNF complex component SNF5 SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1 SWI10 Transcription factor TYE4 Transcription regulatory protein SNF5 TYE4 |
Fig1:
Western blot analysis of SNF5 on different lysates with Rabbit anti-SNF5 antibody (ET7107-84) at 1/1,000 dilution. Lane 1: Daudi cell lysate (20 µg/Lane) Lane 2: PC-12 cell lysate (20 µg/Lane) Lane 3: Human lung tissue lysate (40 µg/Lane) Lane 4: Mouse brain tissue lysate (40 µg/Lane) Lane 5: Rat brain tissue lysate (40 µg/Lane) Predicted band size: 44 kDa Observed band size: 44 kDa Exposure time: Lane 1: 20 seconds; Lane 2-5: 40 seconds; ECL: K1802; 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 (ET7107-84) 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:
Immunocytochemistry analysis of NIH/3T3 cells labeling SNF5 with Rabbit anti-SNF5 antibody (ET7107-84) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-SNF5 antibody (ET7107-84) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (HA601187, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution. |
Fig3:
Immunohistochemical analysis of paraffin-embedded human kidney tissue with Rabbit anti-SNF5 antibody (ET7107-84) at 1/200 dilution. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 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 (ET7107-84) 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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Fig4:
Immunohistochemical analysis of paraffin-embedded mouse large intestine tissue with Rabbit anti-SNF5 antibody (ET7107-84) at 1/500 dilution. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 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 (ET7107-84) at 1/500 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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Fig5: Immunohistochemical analysis of paraffin-embedded rat kidney tissue using anti-SNF5 antibody. Counter stained with hematoxylin. | |
Fig6: Immunohistochemical analysis of paraffin-embedded mouse colon tissue using anti-SNF5 antibody. Counter stained with hematoxylin. |