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Validated All-in-One™ qPCR Primer for PENK(NM_001135690.3) Search again
Product ID:
HQP158510
(click here to view gene annotation page)
Powered by BiozSpecies:
Human
Symbol:
Alias:
PE, PENK-A
Gene Description:
proenkephalin
Target Gene Accession:
NM_001135690.3(click here to view gene page)
Estimated Delivery:
Approximately 1-3 weeks, but may vary. Please email sales@genecopoeia.com or call 301-762-0888 to confirm ETA.
Important Note:
By default, qPCR primer pairs are designed to measure the expression level of the splice variant (accession number) you selected for this gene WITHOUT consideration of other possible variants of this gene. If this gene has multiple variants, and you would like to measure the expression levels of one particular variant, multiple variants, or all variants, please contact us for a custom service project at inquiry@genecopoeia.com.
Gene References into function
- Results suggest that methylation-related inactivation of the ppENK gene is an intermediate or late event during pancreatic carcinogenesis.
- Proenkephalin peptide F has varying immunoreactivity in different circulatory biocompartments after exercise
- Proenkephalin A 119-159 is a stable proenkephalin A precursor fragment identified in human circulation
- The discrete cell-phenotype localization and timing of the changes in the level of PEA and of piGABA-R mRNA.
- Smoking was not associated with p16 or ppENK hypermethylation in pancreatic cancer patients
- study provides evidence that the growth-responsive nuclear protein, proenkephalin (Penk), is required, in part, for apoptosis induction, in response to activation or overexpression of p53 and RelA(p65)
- It found widespread expression of preproenkephalin (pPENK) mRNA and production of the enkephalin precursor protein proenkephalin (PENK) in rat and mouse tissues, as well as in tissues and cells from humans and pigs.
- analysis of polymorphisms of proenkephalin (PENK) and prodynorphin (PDYN) genes in relation to heroin abuse and gene expression in the human striatum and the relevance of genetic dopaminergic tone