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Human LAMP2 ELISA Kit (ab277449)

Human LAMP2 ELISA Kit (ab277449)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Sensitivity: 0.3 ng/ml
  • Range: 0.307 ng/ml - 75 ng/ml
  • Sample type: Cell culture supernatant, Plasma, Serum
  • Detection method: Colorimetric
  • Assay type: Sandwich (quantitative)
  • Reacts with: Human

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Overview

  • Product name

    Human LAMP2 ELISA Kit
    See all LAMP2 kits
  • Detection method

    Colorimetric
  • Precision

    Intra-assay
    Sample n Mean SD CV%
    Overall
    Inter-assay
    Sample n Mean SD CV%
    Overall
  • Sample type

    Cell culture supernatant, Serum, Plasma
  • Assay type

    Sandwich (quantitative)
  • Sensitivity

    0.3 ng/ml
  • Range

    0.307 ng/ml - 75 ng/ml
  • Recovery

    Sample specific recovery
    Sample type Average % Range
    Serum 107.2 86% - 129%
    Plasma 105.1 93% - 117%
    Cell culture media 113 103% - 130%
  • Assay duration

    Multiple steps standard assay
  • Species reactivity

    Reacts with: Human
  • Product overview

    Human LAMP2 ELISA Kit (ab277449) is an in-vitro enzyme-linked immunosorbent assay for the quantitative measurement of Human LAMP2 in serum, plasma and cell culture supernatants.


    This assay employs an antibody specific for Human LAMP2 coated on a 96-well plate. Standards and samples are pipetted into the wells and Human LAMP2 present in a sample is bound to the wells by the immobilized antibody. The wells are washed, and biotinylated anti-Human LAMP2 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 Human LAMP2 bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm.

  • Tested applications

    Suitable for: Sandwich ELISAmore details
  • Platform

    Pre-coated microplate (12 x 8 well strips)

Properties

  • Storage instructions

    Store at -20°C. Please refer to protocols.
  • Components 1 x 96 tests
    150X HRP-Streptavidin Concentrate 1 x 200µl
    20X Wash Buffer Concentrate 1 x 25ml
    5X Assay Diluent B 1 x 15ml
    5X Assay Diluent D 1 x 15ml
    Biotinylated Anti-Human LAMP2 Antibody 2 vials
    Anti-Human LAMP2 coated Microplate 1 unit
    Human LAMP2 standard protein (Lyophilized) 2 vials
    Stop Solution 1 x 8ml
    TMB One-Step Substrate Reagent 1 x 12ml
  • Research areas

    • Tags & Cell Markers
    • Subcellular Markers
    • Organelles
    • Lysosome
    • Signal Transduction
    • Metabolism
    • Energy Metabolism
    • Immunology
    • Secreted Molecules
    • Other secreted molecules
    • Cardiovascular
    • Heart
    • Autophagy
    • Autophagosome
    • Stem Cells
    • Hematopoietic Progenitors
    • Myeloid
    • Myeloid Progenitor
    • Stem Cells
    • Hematopoietic Progenitors
    • Myeloid
    • Monocytic Lineage
    • Metabolism
    • Pathways and Processes
    • Metabolic signaling pathways
    • Energy transfer pathways
    • Energy Metabolism
    • Metabolism
    • Pathways and Processes
    • Metabolism processes
    • Autophagy and mitophagy
    • Autophagosome
    • Cancer
    • Cell Death
    • Autophagy
    • Autophagosome
  • Function

    Implicated in tumor cell metastasis. May function in protection of the lysosomal membrane from autodigestion, maintenance of the acidic environment of the lysosome, adhesion when expressed on the cell surface (plasma membrane), and inter-and intracellular signal transduction. Protects cells from the toxic effects of methylating mutagens.
  • Tissue specificity

    Isoform LAMP-2A is highly expressed in placenta, lung and liver, less in kidney and pancreas, low in brain and skeletal muscle. Isoform LAMP-2B is highly expressed in skeletal muscle, less in brain, placenta, lung, kidney and pancreas, very low in liver.
  • Involvement in disease

    Defects in LAMP2 are the cause of Danon disease (DAND) [MIM:300257]; also known as glycogen storage disease type 2B (GSD2B). DAND is a lysosomal glycogen storage disease characterized by the clinical triad of cardiomyopathy, vacuolar myopathy and mental retardation. It is often associated with an accumulation of glycogen in muscle and lysosomes.
  • Sequence similarities

    Belongs to the LAMP family.
  • Post-translational
    modifications

    O- and N-glycosylated; some of the 16 N-linked glycans are polylactosaminoglycans.
  • Cellular localization

    Cell membrane. Endosome membrane. Lysosome membrane. This protein shuttles between lysosomes, endosomes, and the plasma membrane.
  • Target information above from: UniProt accession P13473 The UniProt Consortium
    The Universal Protein Resource (UniProt) in 2010
    Nucleic Acids Res. 38:D142-D148 (2010) .

    Information by UniProt
  • Alternative names

    • CD107 antigen like family member B
    • CD107 antigen-like family member B
    • CD107b
    • LAMP 2
    • LAMP 2C
    • LAMP-2
    • LAMP2
    • LAMP2_HUMAN
    • LAMPB
    • LGP 96
    • LGP110
    • LGP96
    • Lysosomal associated membrane protein 2
    • Lysosome associated membrane glycoprotein 2
    • Lysosome associated membrane protein 2
    • Lysosome-associated membrane glycoprotein 2
    • Lysosome-associated membrane protein 2
    • MAC3
    see all
  • Database links

    • Entrez Gene: 3920 Human
    • Omim: 309060 Human
    • SwissProt: P13473 Human
    • Unigene: 496684 Human

    Images

    • Example data
      Example data

      These standard curves are for demonstration only. A standard curve must be run with each assay.

    Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
    For licensing inquiries, please contact partnerships@abcam.com

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