Compare | Product No. | Description | SDS | Pricing |
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S7951 | ≥97% (HPLC) | |||
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SML2233 | ≥98% (HPLC) | |||
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I6279 | vial of 10 nmol, monoisotopic mol wt 5,729.6087 Da | |||
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SML2632 | ≥98% (HPLC) | |||
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MABF2791 | 7E7, monoclonal | FACS, IF, IHC (p) | mouse, human | |||||||
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D6790 | ≥95% (HPLC) | |||
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I5523 | powder, ≥27 USP units/mg | |||
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MABN2427 | MW1, monoclonal | ICC, IHC, WB | mouse, rat, human | 4 | ||||||
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MABN1794 | FIG4, monoclonal | DB, ELISA, FACS, IHC, WB | human | |||||||
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286888 | Mobilizes Ca2+ specifically from Ins(1,4,5)P3-sensitive Ca2+ stores by inhibiting microsomal and sarcoplasmic reticulum Ca2+-ATPase activity. | |||
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MAB1920-C | 2E8, monoclonal | ELISA, ICC, IF, WB | mouse, rat, feline, human | |||||||
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539481-M | ||||
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MAB3420-AF555 | PC1C6, monoclonal | ICC, IF | human, rat, bovine, mouse | |||||||
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382065 | Cell-permeable, adenine-thymine-specific fluorescent stain. | |||
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676377 | A cyclododecadepsi-peptide ionophore antibiotic. | |||
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C7249 | ≥98% (HPLC) | |||
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344911 | Acetoxymethyl (AM) derivative of FURA-PE3 with spectral properties similar to the parent compound. | |||
Compare | Product No. | Description | Pricing | |
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495604 | Okadaic Acid, CAS 78111-17-8, is a highly potent inhibitor of protein phosphatase 1 (IC₅₀ = 10-15 nM) and 2A (IC₅₀ = 0.1 nM). | |||
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540411 | Puromycin, CAS 58-58-2, is a protein synthesis inhibitor that causes premature release of nascent polypeptide chains. | |||
Compare | Product No. | Clonality | Application | Species Reactivity | Citations | SDS | ||
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ZRB1245 | 1B13, recombinant monoclonal | FACS, ICC, IHC (p), WB, affinity binding assay | human | |||||
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5.08838 | ||||
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475815-M | Cyclic heptapeptide toxin isolated from the freshwater cyanobacteria Microcystis aeruginosa. | |||
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506350 | ||||
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420321 | Highly specific, cell-permeable, reversible, and ATP-competitive inhibitor of protein kinase G (Ki = 234 nM). | |||