| Description | This product is a human monoclonal antibody that reacts with IL17A. The antibody is expressed with mammalian cell transient expression system, serum-free and purified by affinity chromatography. The purity and integrity are tested via SDS-PAGE and SEC-HPLC analysis. Given an antigen, additional QC measures are also desired such as affinity testing and binding validation. Specifically, the antibody is provided in multiple formats for in vivo and in vitro assays. The Invivo version features greater than 95% purity, ultra-low endotoxin levels (<1 EU/mg or 0.1 EU/mg), and is preservative, stabilizer, and carrier protein-free. |
| Clonality | Monoclonal |
| Host Species | Human |
| Target Species | Human |
| Immunogen | HuIL-17 coupled 10 KLH mixed 1:1 with huIL-17 in Gerbu adjuvant |
| Isotype | IgG |
| Expression Species | HEK293F or CHO |
| Conjugation | None |
| Purity | >95%, determined by SDS-PAGE and/or SEC-HPLC |
| Endotoxin | <1 EU/mg, determined by LAL method |
| Purification | Protein A affinity purified |
| Sterility | 0.2 μM filtered |
| Formulation | PBS, pH 7.4 |
| Preservation | No preservatives |
| Stabilizer | No stabilizers |
| Storage | Store at 4⁰C within a week. For longer storage, aliquot and store at -20⁰C. |
| Application | WB; DB; FC; IP; ELISA; Neut; FuncS; IF; IHC |
| Application Notes | The antibody is recommended for detection of IL17A by FC, IP, ELISA, Neut, FuncS, IF, IHC assays. |
| ELISA | Enzyme-Linked Immunosorbent Assay Protocol |
| WB | Western Blot Protocol |
| FC | Flow Cytometry Protocol |
| Target | IL17A |
| Alternative Name | interleukin 17A; CTLA8, IL17, interleukin 17 (cytotoxic T lymphocyte associated serine esterase 8); interleukin-17A; cytotoxic T lymphocyte associated protein 8; IL 17; IL 17A; CTLA-8; cytotoxic T-lymphocyte-a |
| Gene ID | 3605 |
| UniProt | Q16552 |
| Research Area | Cardiovascular |
Figure 1 Anti-Human IL17A Monoclonal Antibody (V3S-0622-YC1891) in ELISA
ELISA analysis of V3S-0622-YC1891 was performed by coating with Human IL17A Protein (No Tag). Then blocked with BSA and incubated with V3S-0622-YC1891. The HRP-conjugated goat anti-human IgG as a secondary antibody (1: 5000). Detection was performed using TMB substrate and stopped with sulfuric acid. The absorbances were read on a spectrophotometer at 450 nm.
Figure 1 Anti-Human IL17A Monoclonal Antibody (V3S-0622-YC1891) in ELISA
Figure 2 Anti-Human IL17A Monoclonal Antibody (V3S-0622-YC1891) in WB
Western blot analysis of V3S-0622-YC1891 was performed by loading Human IL17A Protein (No Tag) in reduced condition Lane 1, Lane 2 and Lane 3 (0.1 μg, 0.3 μg and 0.6 μg respectively) onto a 12% Tris-HCl polyacrylamide gel. Proteins were transferred to a CN membrane and blocked with 5% skim milk for at least one hour. Membranes were probed with V3S-0622-YC1891 (2 μg/mL) and HRP-conjugated goat anti-human IgG as a secondary antibody (1: 6000). Chemiluminescent detection was performed.
Figure 2 Anti-Human IL17A Monoclonal Antibody (V3S-0622-YC1891) in WB
Figure 3 Anti-Human IL17A Monoclonal Antibody (V3S-0622-YC1891) in DB
Dot Blot analysis of V3S-0622-YC1891 was performed by coating with Human IL17A Protein (No Tag).
V3S-0622-YC1891 incubation concentration: 2 μg/mL.
HRP goat anti-human IgG as a secondary antibody (1: 6000)
NC: Negative control PC: Positive control
Figure 3 Anti-Human IL17A Monoclonal Antibody (V3S-0622-YC1891) in DB
