StarBright Blue 700 and StarBright Blue 520 Fluorescent Secondary Antibodies, and the hFAB Rhodamine Housekeeping Protein Primary Antibodies are part of Bio-Rad’s family of instruments, reagents, and antibodies created to obtain fluorescent western blot results reliably, reproducibly, and with high-quality data. The release of the StarBright 520 Fluorescent Secondary Antibodies completes Bio-Rad’s high-sensitivity triplex western blotting solution. The StarBright Blue 520 Fluorescent Secondary Antibodies can detect low-abundance protein targets in exposure times that are two to four times shorter than those of traditional fluorescent antibodies. It conjugates to highly cross-adsorbed IgG, which leads to low nonspecific binding ![]() The product’s 520 nm emission wavelength means the StarBright Blue 520 Fluorescent Secondary Antibody can pair with a StarBright Blue 700 Fluorescent Secondary Antibody or with other traditional fluorescent antibodies. This property stems from the presence of multiple donor-acceptor pairs in each polymer molecule, which enable it to efficiently absorb and emit light. The StarBright Blue 520 Fluorescent Secondary Antibodies are labeled with a particularly bright fluorescent dye, resulting in short exposure times and a high signal-to-noise ratio. The antibodies work seamlessly on nitrocellulose or low-fluorescence PVDF membranes and all other aspects of the standard western blotting workflow remain unchanged. These plug-and-play antibodies allow simultaneous detection of up to three proteins (two targets of interest and one housekeeping protein) on the same blot when used with the hFAB Rhodamine Housekeeping Protein Fluorescent Primary Antibodies. To address these workflow challenges, Bio-Rad created the StarBright Blue line of secondary antibodies that enable highly sensitive fluorescent detection, short exposure times, and easy multiplexing for western blotting. An alternate method involves attempting to sequentially probe a single blot with multiple fluorescent antibodies to distinguish the signals from each one however, these protocols are cumbersome to optimize and execute. Scientists often resort to cutting or reprobing blots, which introduces variability and results in protein loss, thereby rendering the blot irreproducible and unsuitable for quantitation. ![]() Using traditional chemiluminescent methods to detect and quantify multiple proteins simultaneously can be challenging. They exhibit a two- to threefold lower limit of detection than traditional green emission fluorophore-labeled antibodies such as Alexa Fluor 488 or DyLight 488, the current industry standards. announced the launch of StarBright Blue 520 Fluorescent Secondary Antibodies, fluorescent dye–labeled secondary antibodies for use in multiplex western blotting.
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