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Render Timestamp: 2024-11-21T12:45:47.431Z
Commit: 5c4accf06eb7154018ba3f54329c7590f97f534a
XML generation date: 2024-09-30 01:55:26.284
Product last modified at: 2024-11-18T23:45:07.594Z
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PDP - Template Name: Monoclonal Antibody
PDP - Template ID: *******c5e4b77
  1. Products /
  2. Primary Antibodies /
  3. BNIP3 (D7U1T) Rabbit mAb
R Recombinant
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.

BNIP3 (D7U1T) Rabbit mAb #44060

Filter:
  • WB
  • IP
  • IHC
  • IF

    Supporting Data

    REACTIVITY H
    SENSITIVITY Endogenous
    MW (kDa) 22-28, 50-55
    Source/Isotype Rabbit IgG
    Application Key:
    • WB-Western Blotting 
    • IP-Immunoprecipitation 
    • IHC-Immunohistochemistry 
    • IF-Immunofluorescence 
    Species Cross-Reactivity Key:
    • H-Human 

    Product Information

    Product Usage Information

    Application Dilution
    Western Blotting 1:1000
    Immunoprecipitation 1:100
    Immunohistochemistry (Paraffin) 1:100
    Immunofluorescence (Immunocytochemistry) 1:800

    Storage

    Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.

    Protocol

    Specificity / Sensitivity

    BNIP3 (D7U1T) Rabbit mAb recognizes endogenous levels of total BNIP3 protein.

    Species Reactivity:

    Human

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues near the amino terminus of human BNIP3 protein.

    Background

    BNIP3 (Bcl-2/E1B-19kDa interacting protein 3) is a pro-apoptotic mitochondrial protein and Bcl-2 family member that contains a Bcl-2 homology 3 (BH3) domain and a carboxyl-terminal transmembrane (TM) domain (1-3). While BNIP3 has a predicted molecular weight of about 22 kDa, it runs anomalously on SDS-PAGE and includes a band of around 60 kDa that may be a dimeric form that is not reduced (2). BNIP3 associates with anti-apoptotic family members Bcl-2, Bcl-xL, and the adenovirus homologue E1B-19kDa. BNIP3 is distinct from other Bcl-2 family members that contain only the BH3 domain in that the TM domain, and not the BH3 domain, is required for mitochondrial targeting and pro-apoptotic activity (4). In addition to apoptosis, BNIP3 has been implicated in necrosis (5) and autophagy (6-11). In hypoxic conditions, BNIP3 can induce mitochondrial autophagy (mitophagy) by disrupting the Bcl-2-Beclin-1 complex (9). BNIP3 can also promote mitophagy by triggering the translocation of the E3 ubiquitin ligase Parkin to the mitochondria (10) or by directly binding LC3 on the autophagosome (11). BNIP3 may also localize to the endoplasmic reticulum (ER) where it can selectively induce the autophagic clearance of ER (ERphagy) (11). Increased expression of BNIP3 under hypoxic conditions is mainly regulated by the transcription factor HIF-1α (12-14). Silencing of the BNIP3 promoter by methylation has been observed in several types of cancer cells and may play an important role in their survival (14-18).
    1. Boyd, J.M. et al. (1994) Cell 79, 341-51.
    2. Chen, G. et al. (1997) J Exp Med 186, 1975-83.
    3. Yasuda, M. et al. (1998) J Biol Chem 273, 12415-21.
    4. Ray, R. et al. (2000) J Biol Chem 275, 1439-48.
    5. Vande Velde, C. et al. (2000) Mol Cell Biol 20, 5454-68.
    6. Daido, S. et al. (2004) Cancer Res 64, 4286-93.
    7. Tracy, K. et al. (2007) Mol Cell Biol 27, 6229-42.
    8. Quinsay, M.N. et al. (2010) Autophagy 6, 855-62.
    9. Bellot, G. et al. (2009) Mol Cell Biol 29, 2570-81.
    10. Lee, Y. et al. (2011) Am J Physiol Heart Circ Physiol 301, H1924-31.
    11. Hanna, R.A. et al. (2012) J Biol Chem 287, 19094-104.
    12. Bruick, R.K. (2000) Proc Natl Acad Sci USA 97, 9082-7.
    13. Guo, K. et al. (2001) Cell Death Differ 8, 367-76.
    14. Sowter, H.M. et al. (2001) Cancer Res 61, 6669-73.
    15. de Angelis, P.M. et al. (2004) Int J Oncol 24, 1279-88.
    16. Okami, J. et al. (2004) Cancer Res 64, 5338-46.
    17. Murai, M. et al. (2005) Clin Cancer Res 11, 1021-7.
    18. Murai, M. et al. (2005) Br J Cancer 92, 1165-72.

    Database Links

    UniProt ID: Q12983


    Entrez-Gene Id: 664


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