Anti-Parkin monoclonal antibody (DMAB6629)

Mouse anti-Human Parkin monoclonal antibody for ICC, IP Datasheet

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Host Species
Antibody Isotype
Species Reactivity
Synthetic peptide of the C-terminal part of human parkin (AYRVDERAAEQARWEAA).


Alternative Names
Entrez Gene ID
UniProt ID

Product Background

Gene summary
PARK2 (Parkin RBR E3 Ubiquitin Protein Ligase) is a Protein Coding gene. Diseases associated with PARK2 include parkinson disease, juvenile, type 2 and leprosy. Among its related pathways are Transport to the Golgi and subsequent modification and Immune System. GO annotations related to this gene include identical protein binding and enzyme binding. The precise function of this gene is unknown; however, the encoded protein is a component of a multiprotein E3 ubiquitin ligase complex that mediates the targeting of substrate proteins for proteasomal degradation. Mutations in this gene are known to cause Parkinson disease and autosomal recessive juvenile Parkinson disease. Alternative splicing of this gene produces multiple transcript variants encoding distinct isoforms. Additional splice variants of this gene have been described but currently lack transcript support.


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Orimo, S; Amino, T; et al. Preserved cardiac sympathetic nerve accounts for normal cardiac uptake of MIBG in PARK2. MOVEMENT DISORDERS 20:1350-1353(2005).
Ramsey, CP; Giasson, BI; et al. Identification and characterization of a novel endogenous murine parkin mutation. JOURNAL OF NEUROCHEMISTRY 113:402-417(2010).

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We offer labeled antibodies using our catalogue antibody products and a broad range of intensely fluorescent dyes and labels including HRP, biotin, ALP, Alexa Fluor® dyes, DyLight® Fluor dyes, R-phycoerythrin (R-PE), at scales from less than 100 μg up to 1 g of IgG antibody. Learn More

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