IRAK-M Antibody (XX-6) recommended for detection of IRAK-M of human origin by WB, IP and ELISA

IRAK-M Antibody (XX-6): sc-100389

IRAK-M Antibody (XX-6) is rated 5.0 out of 5 by 3.
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Datasheets

    • Anti-IRAK-M Antibody (XX-6) is a mouse monoclonal IgG1 (kappa light chain) IRAK-M antibody provided at 100 µg/ml
    • raised against a partial recombinant protein mapping within amino acids 497-596 of IRAK-M of human origin
    • recommended for detection of IRAK-M of human origin by WB, IP and ELISA
    • See m-IgGκ BP-HRP (mouse IgGκ binding protein-HRP), our highly recommended recombinant alternative to conventional secondary anti-mouse IgG reagents.
    • Contact our Technical Service Department (or your local Distributor) for more information on how to receive a FREE 10 µg sample of IRAK-M (XX-6): sc-100389.

i got two bands in THP-1 cells with this antibody, one is less signal at ~70kDa, another very stronger band is located at ~50kDa, is that correct?

Asked by: Hui1019
Thank you for your question. Please contact our Technical Service Department for assistance in troubleshooting this antibody.
Answered by: Technical Support
Date published: 2018-12-11

I need to use an antibody to detect the protein in samples of equine origin. Do you know if this mouse monoclonal antibody will work?

Asked by: jerojero
Please contact our Technical Service Department and we would be happy to perform sequence analysis and review our data to answer any questions you may have about additional species reactivity.
Answered by: Technical Support 7
Date published: 2017-02-15
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Rated 5 out of 5 by from Good IRAK-M antibody for WB Works well in western blotting for IRAK-M in primary human monocytes. Strong band easily visualised with only a few very minor background bands.
Date published: 2018-04-17
Rated 5 out of 5 by from Clean blot! Single band seen in Western Blot for IRAK-M, with no additional banding.
Date published: 2017-01-20
Rated 5 out of 5 by from Great Great, crisp band seen in WB using HeLa whole cell lysate. -SCBT QC
Date published: 2013-04-16
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