• Product nameAnti-AP1S2 antibody
  • Description
    Rabbit polyclonal to AP1S2
  • Tested applicationsSuitable for: WBmore details
  • Species reactivity
    Reacts with: Human
    Predicted to work with: Mouse, Cow, Zebrafish
  • Immunogen

    Recombinant fragment containing a sequence corresponding to a region within amino acids 1-122 of Human AP1S2 (NP_003907).

  • Positive control
    • Raji whole cell lysate; A431 cell lysate


  • FormLiquid
  • Storage instructionsShipped at 4°C. Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
  • Storage bufferPreservative: 0.01% Thimerosal (merthiolate)
    Constituents: 10% Glycerol, 0.1M Tris, 0.1M Glycine, pH 7.0
  • Concentration information loading...
  • PurityImmunogen affinity purified
  • ClonalityPolyclonal
  • IsotypeIgG
  • Research areas

Associated products


Our Abpromise guarantee covers the use of ab97590 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 - 1/3000. Predicted molecular weight: 19 kDa.


  • FunctionSubunit of clathrin-associated adaptor protein complex 1 that plays a role in protein sorting in the late-Golgi/trans-Golgi network (TGN) and/or endosomes. The AP complexes mediate both the recruitment of clathrin to membranes and the recognition of sorting signals within the cytosolic tails of transmembrane cargo molecules.
  • Tissue specificityWidely expressed.
  • Involvement in diseaseDefects in AP1S2 are the cause of mental retardation X-linked type 59 (MRX59) [MIM:300630]. It is characterized by significantly sub-average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period. In contrast to syndromic or specific X-linked mental retardation which also present with associated physical, neurological and/or psychiatric manifestations, intellectual deficiency is the only primary symptom of non-syndromic X-linked mental retardation. MRX59 consists of a mild-to-profound mental retardation. Other features includes hypotonia early in life and delay in walking.
  • Sequence similaritiesBelongs to the adaptor complexes small subunit family.
  • Cellular localizationGolgi apparatus. Cytoplasmic vesicle membrane. Membrane > clathrin-coated pit. Component of the coat surrounding the cytoplasmic face of coated vesicles located at the Golgi complex.
  • Information by UniProt
  • Database links
  • Alternative names
    • Adapter related protein complex 1 sigma 1B subunit antibody
    • Adapter-related protein complex 1 sigma-1B subunit antibody
    • Adaptor protein complex AP 1 sigma 1B subunit antibody
    • Adaptor protein complex AP-1 sigma-1B subunit antibody
    • Adaptor related protein complex 1 sigma 2 subunit antibody
    • AP 1 complex subunit sigma 2 antibody
    • AP-1 complex subunit sigma-2 antibody
    • ap1s2 antibody
    • AP1S2_HUMAN antibody
    • Clathrin adaptor complex AP1 sigma 1B subunit antibody
    • Clathrin assembly protein complex 1 sigma 1B small chain antibody
    • Clathrin assembly protein complex 1 sigma-1B small chain antibody
    • Clathrin associated assembly adaptor protein small 1 like antibody
    • DC22 antibody
    • Golgi adaptor HA1 AP1 adaptin sigma 1B subunit antibody
    • Golgi adaptor HA1/AP1 adaptin sigma-1B subunit antibody
    • mental retardation X linked 59 antibody
    • MGC:1902 antibody
    • MRX59 antibody
    • Sigma 1B subunit of AP 1 clathrin antibody
    • Sigma 1B subunit of AP-1 clathrin antibody
    • Sigma adaptin 1B antibody
    • Sigma-adaptin 1B antibody
    • Sigma1B adaptin antibody
    • SIGMA1B antibody
    • Sigma1B-adaptin antibody
    see all

Anti-AP1S2 antibody images

  • Anti-AP1S2 antibody (ab97590) at 1/1000 dilution + Raji whole cell lysate at 30 µg

    Predicted band size : 19 kDa

References for Anti-AP1S2 antibody (ab97590)

ab97590 has not yet been referenced specifically in any publications.

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