• Product name
    Human LIMP II ELISA Kit
  • Detection method
  • Sample type
    Cell culture supernatant, Serum, Plasma
  • Assay type
    Sandwich (quantitative)
  • Sensitivity
    < 10 pg/ml
  • Range
    10.24 pg/ml - 2500 pg/ml
  • Recovery

    86 %

    Sample specific recovery
    Sample type Average % Range
    Cell culture supernatant 95.06 74% - 107%
    Serum 83 74% - 92%
    Plasma 79.65 71% - 86%

  • Assay duration
    Multiple steps standard assay
  • Species reactivity
    Reacts with: Human
  • Product overview

    Abcam’s LIMP II Human ELISA (Enzyme-Linked Immunosorbent Assay) kit is an in vitro enzyme-linked immunosorbent assay for the quantitative measurement of Human LIMP-II in serum, plasma, cell culture supernatants.

    This assay employs an antibody specific for Human LIMP II coated on a 96-well plate. Standards and samples are pipetted into the wells and LIMP II present in a sample is bound to the wells by the immobilized antibody. The wells are washed and biotinylated anti-Human LIMP II antibody is added. After washing away unbound biotinylated antibody, HRP-conjugated streptavidin is pipetted to the wells. The wells are again washed, a TMB substrate solution is added to the wells and color develops in proportion to the amount of LIMP II bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm.

  • Notes

    Optimization may be required with urine samples.

  • Tested applications
    Suitable for: Sandwich ELISAmore details
  • Platform


  • Storage instructions
    Store at -20°C. Please refer to protocols.
  • Components 1 x 96 tests
    200X HRP-Streptavidin Concentrate 1 x 200µl
    20X Wash Buffer Concentrate 1 x 25ml
    5X Assay Diluent B 1 x 15ml
    Assay Diluent C 1 x 30ml
    Biotinylated anti-Human LIMP II 2 vials
    LIMP II Microplate (12 strips x 8 wells) 1 unit
    Recombinant Human LIMP II Standard 2 vials
    Stop Solution 1 x 8ml
    TMB One-Step Substrate Reagent 1 x 12ml
  • Research areas
  • Function
    Act as a lysosomal receptor for glucosylceramidase (GBA) targeting.
  • Involvement in disease
    Defects in SCARB2 are the cause of progressive myoclonic epilepsy type 4 with or without renal failure (EPM4) [MIM:254900]. An autosomal recessive progressive myoclonic epilepsy associated with renal failure in some cases. Cognitive function is preserved. Myoclonus is a brief, involuntary twitching of a muscle or a group of muscles. Cognitive function is preserved.
    Note=Genetic variants in SCARB2 can act as modifier of the phenotypic expression and severity of Gaucher disease.
  • Sequence similarities
    Belongs to the CD36 family.
  • Cellular localization
    Lysosome membrane.
  • Information by UniProt
  • Alternative names
    • 85 kDa lysosomal membrane sialoglycoprotein
    • CD36
    • CD36 antigen-like 2
    • LGP85
    • LIMP II
    • Lysosome membrane protein 2
    • Lysosome membrane protein II
    • Scarb2
    • Scavenger receptor class B member 2
    see all
  • Database links


Our Abpromise guarantee covers the use of ab113336 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
Sandwich ELISA Use at an assay dependent concentration.


  • Representative Standard Curve using ab113336



ab113336 has not yet been referenced specifically in any publications.

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