Overview

  • Product name

  • Description

    Goat polyclonal to Hemopexin
  • Host species

    Goat
  • Tested applications

    Suitable for: WBmore details
  • Species reactivity

    Reacts with: Human
    Predicted to work with: Orangutan
  • Immunogen

    Synthetic peptide corresponding to Human Hemopexin aa 32-45 (internal sequence) (Cysteine residue). (NP_000604.1)
    Sequence:

    C-HGNVAEGETKPDPD


    Database link: P02790

  • Positive control

    • WB: Human placenta lysate.

Properties

Applications

Our Abpromise guarantee covers the use of ab223210 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
WB Use a concentration of 0.1 - 0.3 µg/ml. Detects a band of approximately 80 kDa (predicted molecular weight: 52 kDa).

Target

  • Function

    Binds heme and transports it to the liver for breakdown and iron recovery, after which the free hemopexin returns to the circulation.
  • Tissue specificity

    Expressed by the liver and secreted in plasma.
  • Sequence similarities

    Belongs to the hemopexin family.
    Contains 5 hemopexin-like domains.
  • Post-translational
    modifications

    N- and O-glycosylated. O-glycosylated with core 1 or possibly core 8 glycans.
  • Cellular localization

    Secreted.
  • Information by UniProt
  • Database links

  • Alternative names

    • Beta 1B glycoprotein antibody
    • Beta-1B-glycoprotein antibody
    • FLJ56652 antibody
    • HEMO antibody
    • HEMO_HUMAN antibody
    • Hemopexin antibody
    • Hpx antibody
    • HX antibody
    see all

Images

  • Anti-Hemopexin antibody (ab223210) at 0.1 µg/ml + Human placenta lysate (in RIPA buffer) at 35 µg

    Developed using the ECL technique.

    Predicted band size: 52 kDa
    Observed band size: 80 kDa
    why is the actual band size different from the predicted?



    Primary incubation was 1 hour.

References

ab223210 has not yet been referenced specifically in any publications.

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