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Alomone Labs offers one of the most comprehensive, in-house-made portfolios of primary antibodies in the ion channel field, generated in rabbit, mouse, and guinea pig hosts covering voltage-gated and ligand-gated ion channels, regulatory subunits, and related proteins. All antibodies are produced and rigorously validated internally, ensuring high specificity and consistent performance across applications such as Western blotting, immunohistochemistry, immunocytochemistry, flow cytometry, and more. To further support advanced imaging and multiplexing, we also provide a growing selection of fluorophore-conjugated antibody options. This extensive suite of in-house products empowers researchers to precisely detect, visualize, and characterize ion channel expression and function in diverse biological systems.
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The expected molecular weight (MW) listed in the product datasheet is based solely on the size of the target protein’s amino acid sequence. It’s important to remember that many factors can affect the banding pattern of your western blot including: (1) the existence of a splice variant, (2) the quality of the loaded sample, (3) the protein extraction method, and (4) the protein transfer conditions. To achieve accurate results, you may need to systematically adjust the protein extraction method or the protein transfer conditions.
Some toxins and peptides are soluble in DMSO; you can find this information in the product specification section. For these products, prepare a concentrated stock solution first.
Note: We recommend that you maintain a DMSO concentration as low as possible. For cell assays, a final concentration of 0.1–0.5% DMSO (v/v) is considered acceptable. For other experiments, 5% DMSO (v/v) is recommended; adjust this according to your experimental requirements.
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