Overview

  • Product nameAnti-VPS53 antibody
    See all VPS53 primary antibodies
  • Description
    Mouse polyclonal to VPS53
  • SpecificityThis antibody is reactive against mammalian transfected lysate.
  • Tested applicationsSuitable for: WBmore details
  • Species reactivity
    Reacts with: Human
  • Immunogen

    VPS53 (NP_060759, 1 a.a. ~ 670 a.a) full-length human protein.

  • Positive control
    • Transfected 293T cell lysate.

Properties

Applications

Our Abpromise guarantee covers the use of ab69422 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 1/500 - 1/1000. Detects a band of approximately 76 kDa (predicted molecular weight: 76 kDa).

Target

  • FunctionMay be involved in retrograde transport of early and late endosomes to the late Golgi.
  • Sequence similaritiesBelongs to the VPS53 family.
  • Cellular localizationGolgi apparatus > trans-Golgi network membrane. Endosome membrane.
  • Information by UniProt
  • Database links
  • Alternative names
    • FLJ10979 antibody
    • FLJ41112 antibody
    • FLJ61757 antibody
    • HCCS1 antibody
    • hVps53L antibody
    • MGC39512 antibody
    • pp13624 antibody
    • Vacuolar protein sorting 53 (yeast) antibody
    • Vacuolar protein sorting 53 antibody
    • Vacuolar protein sorting 53 homolog (S. cerevisiae) antibody
    • Vacuolar protein sorting-associated protein 53 homolog antibody
    • VPS53 antibody
    • VPS53_HUMAN antibody
    see all

Anti-VPS53 antibody images

  • All lanes : Anti-VPS53 antibody (ab69422) at 1/500 dilution

    Lane 1 : VPS53 transfected 293T cell lysate
    Lane 2 : Non-transfected 293T cell lysate

    Lysates/proteins at 25 µg per lane.

    Secondary
    Goat Anti-Mouse IgG (H&L)-HRP Conjugate at 1/2500 dilution

    Predicted band size : 76 kDa
    Observed band size : 76 kDa

References for Anti-VPS53 antibody (ab69422)

ab69422 has not yet been referenced specifically in any publications.

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