Render Target: STATIC
Render Timestamp: 2024-11-12T10:29:28.485Z
Commit: 3c1f305a63297e594ac8d7bb5424007d592d68be
XML generation date: 2024-08-01 15:24:39.270
Product last modified at: 2024-08-28T22:15:07.701Z
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PDP - Template Name: Polyclonal Antibody
PDP - Template ID: *******59c6464

NDRG2 Antibody #5667

Filter:
  • WB

    Supporting Data

    REACTIVITY H M R
    SENSITIVITY Endogenous
    MW (kDa) 45
    SOURCE Rabbit
    Application Key:
    • WB-Western Blotting 
    Species Cross-Reactivity Key:
    • H-Human 
    • M-Mouse 
    • R-Rat 

    Product Information

    Product Usage Information

    Application Dilution
    Western Blotting 1:1000

    Storage

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

    Protocol

    Specificity / Sensitivity

    NDRG2 Antibody recognizes endogenous levels of total NDRG2 protein.

    Species Reactivity:

    Human, Mouse, Rat

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Lys25 of human NDRG2 protein. Antibodies are purified by protein A and peptide affinity chromatography.

    Background

    The NDRG (N-Myc downstream-regulated gene) family consisting of NDRG1, NDRG2, NDRG3, and NDRG4 are structurally related proteins with roles in cell proliferation, differentiation, apoptosis, stress responses, and cell migration/metastasis (1-3). NDRG1 was originally identified as a protein that was upregulated in N-Myc knockout mice (1). Proteins in the NDRG family, particularly NDRG1 and NDRG2, have been reported to be down-regulated in various cancer tissues and have been suggested to function as a tumor suppressors (4,5).
    Expression of NDRG1 and NDRG2 is up-regulated by p53 and HIF-1, and contributes to apoptosis driven by those pathways (6-11). NDRG1 and NDRG2 are also associated with pathological conditions in the nervous system. Nonsense mutation of the NDRG1 gene has been shown to cause hereditary motor and sensory neuropathy-Lom (HMSNL), which is supported by studies demonstrating the role of NDRG1 in maintaining myelin sheaths and axonal survival (12, 13). Elevated expression of NDRG2 has been observed with Alzheimer's disease (14). Both NDGR1 and NDGR2 are phosphorylated at multiple sites by Akt and/or SGK1, although the precise physiological role of this phosphorylation is not known (15, 16).
    1. Shimono, A. et al. (1999) Mech Dev 83, 39-52.
    2. Qu, X. et al. (2002) Mol Cell Biochem 229, 35-44.
    3. Zhou, R.H. et al. (2001) Genomics 73, 86-97.
    4. Yao, L. et al. (2008) Acta Biochim Biophys Sin (Shanghai) 40, 625-35.
    5. Ellen, T.P. et al. (2008) Carcinogenesis 29, 2-8.
    6. Kurdistani, S.K. et al. (1998) Cancer Res 58, 4439-44.
    7. Park, H. et al. (2000) Biochem Biophys Res Commun 276, 321-8.
    8. Stein, S. et al. (2004) J Biol Chem 279, 48930-40.
    9. Cangul, H. (2004) BMC Genet 5, 27.
    10. Wang, L. et al. (2008) Cell Physiol Biochem 21, 239-50.
    11. Liu, N. et al. (2008) Nucleic Acids Res 36, 5335-49.
    12. Kalaydjieva, L. et al. (2000) Am J Hum Genet 67, 47-58.
    13. Okuda, T. et al. (2004) Mol Cell Biol 24, 3949-56.
    14. Mitchelmore, C. et al. (2004) Neurobiol Dis 16, 48-58.
    15. Murray, J.T. et al. (2004) Biochem J 384, 477-88.
    16. Burchfield, J.G. et al. (2004) J Biol Chem 279, 18623-32.
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