Antibody conjugation kits from Novus simplify the antibody labeling process. You can now label almost any primary antibody in less than 30 seconds hands-on time. Choose from over 40 enzymatic, fluorescent, or biotin labels for use in western blot, immunohistochemistry, flow cytometry, or your application of choice.
Alexa Fluor - 488, 555, 568, 594, 647, 700
Atto – 390, 488, 565, 633, 700
Cyanine Dye - Cy3, Cy5, Cy5.5
DyLightTM - 350, 405, 488, 550, 594, 633, 650, 680, 755, 800
The presence of low molecular weight substances in commercially available antibodies impacts the efficiency of the labeling process. Common antibody additives such as BSA, glycine, and azide contain lysine residues. As the majority of labeling methods exploit the lysine residue, forming a strong bond between the lysine and conjugate, any primary amine containing additive will be conjugated during the labeling reaction.
For efficient labeling, we recommend an antibody be greater than 95% pure and at a concentration greater than 0.5 mg/ml. We do not recommend conjugating antibodies harvested from ascites fluid, crude serum, or hybridoma culture supernatant. These antibodies contain protein and cell culture nutrients (amino acids) that impact conjugation. If your antibody is provided in one of these formulations, we recommend a purification or concentration step to remove unwanted additives prior to antibody labeling.
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