Overview

Properties

Associated products

Applications

Our Abpromise guarantee covers the use of ab11928 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 1 - 2 µg/ml. Detects a band of approximately 45 kDa.

Target

  • FunctionInvolved in mediating interferon-gamma-induced cell death.
  • Tissue specificityUbiquitous.
  • Cellular localizationMitochondrion.
  • Information by UniProt
  • Database links
  • Alternative names
    • 28S ribosomal protein S29 antibody
    • 28S ribosomal protein S29 mitochondrial antibody
    • bMRP10 antibody
    • DAP 3 antibody
    • DAP-3 antibody
    • Dap3 antibody
    • Death associated protein 3 antibody
    • Death-associated protein 3 antibody
    • DKFZp686G12159 antibody
    • FLJ12817 antibody
    • Ionizing radiation resistance conferring protein antibody
    • MGC126058 antibody
    • MGC126059 antibody
    • Mitochondrial 28S ribosomal protein S29 antibody
    • mitochondrial antibody
    • MITOCHONDRIAL RIBOSOMAL PROTEIN S29 antibody
    • MRP S29 antibody
    • MRP-S29 antibody
    • MRPS29 antibody
    • OTTHUMP00000033480 antibody
    • OTTHUMP00000033481 antibody
    • PSD-95/SAP90-binding protein 3 antibody
    • RT29_HUMAN antibody
    • S29mt antibody
    • SAP90/PSD-95-associated protein 3 antibody
    • SAPAP3 antibody
    see all

Anti-DAP3 antibody [42C617] images

  • Anti-DAP3 antibody [42C617] (ab11928) at 2 µg/ml + HepG2 (Human hepatocellular liver carcinoma cell line) Whole Cell Lysate at 10 µg

    Secondary
    Goat polyclonal to Mouse IgG - H&L - Pre-Adsorbed (HRP) at 1/3000 dilution

    Observed band size : 43 kDa (why is the actual band size different from the predicted?)

References for Anti-DAP3 antibody [42C617] (ab11928)

This product has been referenced in:
  • Hornig-Do HT  et al. Human mitochondrial leucyl tRNA synthetase can suppress non cognate pathogenic mt-tRNA mutations. EMBO Mol Med 6:183-93 (2014). WB ; Human . Read more (PubMed: 24413189) »
  • Carroll CJ  et al. Whole-exome sequencing identifies a mutation in the mitochondrial ribosome protein MRPL44 to underlie mitochondrial infantile cardiomyopathy. J Med Genet 50:151-9 (2013). Read more (PubMed: 23315540) »

See all 6 Publications for this product

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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"