IL-17 Rabbit Polyclonal Antibody
cat.: ER1706-91
| Product Type: | Rabbit polyclonal IgG, primary antibodies |
|---|---|
| Species reactivity: | Human |
| Applications: | WB, IHC-P, FC |
| Clonality: | Polyclonal |
| Form: | Liquid |
| Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles. |
| Storage buffer: | 1*PBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide. |
| Concentration: | 1ug/ul |
| Purification: | Immunogen affinity purified. |
| Molecular weight: | Predicted band size: 18 kDa |
| Isotype: | IgG |
| Immunogen: | Synthetic peptide within Human IL-17 aa 60-109 / 155. |
| Positive control: | Human tonsil tissue, Jurkat. |
| Subcellular location: | Secreted. |
| Recommended Dilutions:
WB IHC-P FC |
1:500-1:2000 1:1,000 1:50-1:100 |
| Uniprot #: | SwissProt: Q16552 Human | Q61453 Rat |
| Alternative names: | CTLA 8 CTLA-8 CTLA8 Cytotoxic T lymphocyte associated antigen 8 Cytotoxic T lymphocyte associated protein 8 Cytotoxic T lymphocyte associated serine esterase 8 Cytotoxic T-lymphocyte-associated antigen 8 IL 17A IL-17 IL-17A IL17 IL17_HUMAN Il17a Interleukin 17 (cytotoxic T lymphocyte associated serine esterase 8) Interleukin 17A Interleukin-17A Interleukin17 Interleukin17A OTTHUMP00000016597 OTTMUSP00000046003 |
Images
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Fig1:
Western blot analysis of IL-17 on IL-17 recombinant protein with Rabbit anti-IL-17 antibody (ER1706-91) at 1/1,000 dilution. Lysates/proteins at 50 ng/Lane. Predicted band size: 18 kDa Observed band size: 16 kDa Exposure time: 10 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 (ER1706-91) 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. |
|
Fig2:
Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Rabbit anti-IL-17 antibody (ER1706-91) 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 (ER1706-91) 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. |
|
Fig3: Flow cytometric analysis of Jurkat cells with IL-17 antibody at 1/100 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black). |
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.