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PREPL Antibody (C-term) Blocking peptide

Synthetic peptide

     
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Product Information
Primary Accession Q4J6C6
Other Accession NP_006027.2
Clone Names 91102219
Additional Information
Gene ID 9581
Other Names Prolyl endopeptidase-like, 3421-, Prolylendopeptidase-like, PREPL, KIAA0436
Format Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
StorageMaintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.
PrecautionsThis product is for research use only. Not for use in diagnostic or therapeutic procedures.
Protein Information
Name PREPL
Synonyms KIAA0436
Function Serine peptidase whose precise substrate specificity remains unclear (PubMed:16143824, PubMed:16385448, PubMed:28726805). Does not cleave peptides after a arginine or lysine residue (PubMed:16143824). Regulates trans-Golgi network morphology and sorting by regulating the membrane binding of the AP-1 complex (PubMed:23321636). May play a role in the regulation of synaptic vesicle exocytosis (PubMed:24610330).
Cellular Location Cytoplasm, cytosol. Golgi apparatus, trans-Golgi network {ECO:0000250|UniProtKB:Q8C167}. Cytoplasm, cytoskeleton {ECO:0000250|UniProtKB:Q8C167}. Golgi apparatus {ECO:0000250|UniProtKB:Q8C167}. Nucleus Note=Co-localizes with AP-1 in the trans-Golgi network (By similarity) Co-localizes with MAP2 and ACTB on the cytoskeleton (By similarity) Co-localizes with STX6 and GOSR2 at the Golgi apparatus (By similarity). {ECO:0000250|UniProtKB:Q8C167}
Tissue Location Expressed in pyramidal neurons of the temporal cortex and neocortex (at protein level) (PubMed:23485813). Widely expressed (PubMed:15913950, PubMed:16385448). Expressed at higher level in brain, skeletal muscle, heart and kidney (PubMed:15913950, PubMed:16385448). Expressed at the endplates in the neuromuscular junction (PubMed:24610330).
Research Areas
Citations (0)
citation

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Background

The protein encoded by this gene belongs to the prolyloligopeptidase subfamily of serine peptidases. Mutations in thisgene have been associated with hypotonia-cystinuria syndrome, alsoknown as the 2p21 deletion syndrome.

References

Parvari, R., et al. Genomics 86(2):195-211(2005)Kim, D.K., et al. Biochim. Biophys. Acta 1565(1):112-121(2002)Parvari, R., et al. Am. J. Hum. Genet. 69(4):869-875(2001)Robertson, N.G., et al. Genomics 23(1):42-50(1994)

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$ 277.78
Cat# BP5565b
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