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How is PIN1 fused to its partner? (A01090 PIN1 Antibody, pAb, Rabbit)
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Is there any cross-reactivity between the fusion partner and PIN1? (A01090 PIN1 Antibody, pAb, Rabbit)
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What is the fusion partner? (A01090 PIN1 Antibody, pAb, Rabbit)
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The MW of the target protein is about 18 kDa, so why is the band in the WB test picture almost 60 kDa. (A01090 PIN1 Antibody, pAb, Rabbit)
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In which species does antibody A01622 (GAPDH Antibody, mAb, Mouse) recognize GAPDH?
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Does Catalog No. A00160 (Goat Anti-Mouse IgG Antibody (H&L) [HRP], pAb) cross react with rabbit?
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Is Catalog No. A00166 (Goat Anti-Human IgG Antibody (H&L) [HRP], pAb) specific for human IgG. Does it cross-react with non-human primates or rodents?
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I've purchased A01428-100 (THE™ DYKDDDDK Tag Antibody [HRP], mAb, Mouse). I was wondering if the presence of HRP will interfere with secondary antibody binding (either Goat anti-Mouse secondary or Protein G secondary).
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Do you have any information on antibody stability after reconstitution? I'm concerned that an IgM antibody may have fragmented during the lyophilization process or became aggregated upon reconstitution.
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Can I use A01795 (THE™ PEG Antibody, mAb, Mouse) in building an affinity column.
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Can A01795 (THE™ PEG Antibody, mAb, Mouse) recognize PEG5?
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I need a rabbit anti-His tag antibody which can recognize a His-tag fused on an internal site of a protein. I want to perform Flow Cytometry with this antibody. Which antibody should I use?
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We are using your ELISA kit L00436 (His Tag ELISA Detection Kit) and we like to use the same anti-His monoclonal antibody for western blot. What is the Catalog No. for the mAb used in the L00436 ELISA kit? What is its recommended concentration for WB?
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For A00186 (THE™ His Tag Antibody, mAb, Mouse), what is the working concentration range for Immunofluorescence?
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Which antibody should I use to detect a very small amount of His protein in a Flow Cytometry assay?
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Will using a brighter fluorophore allow better detection of a molecule on a cell that is in low abundance?
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How do you guarantee the quality of the antibodies?
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In general, how should I preserve the antibody?
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When I analyze cytoplasmic protein detection by FACS, the result is negative. However the result is positive when analyzing by Western Blot showing a band with the right M.W. What is the possible reason?
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The protein band in the western blot is different from the predicted molecular weight of the protein. What might be the possible reason?
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What are the reasons for high background in WB test?
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Do you have any antibody products mainly designed for pharmaceutical manufactures?
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In general, what is the recommended working concentration of your primary antibody?
