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Validated All-in-One™ qPCR Primer for EMSY(NM_020193.5) Search again
Product ID:
HQP179419
(click here to view gene annotation page)
Species:
Human
Symbol:
Alias:
C11orf30, GL002
Gene Description:
EMSY transcriptional repressor, BRCA2 interacting
Target Gene Accession:
NM_020193.5(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
- The remarkable clinical overlap between sporadic EMSY amplification and familial BRCA2 deletion implicates a BRCA2 pathway in sporadic breast and ovarian cancer.
- The crystal structure of residues 1-108 of EMSY at 2.0 A resolution is reported; the structure contains both the ENT domain and the HP1beta/BS69-binding motif.
- report the crystal structure of the ENT domain of EMSY; dimerisation of EMSY mediated by the ENT domain could provide flexibility for it to bind two or more different substrates simultaneously
- common genetic variation in EMSY does not appear to have a role in development of breast or ovarian cancer
- These results support the hypothesis that EMSY overexpression can play a role in the genesis of human breast cancer.
- Findings support the role of EMSY as a key oncogene within the 11q13 amplicon in ovarian cancer.
- In an ovarian carcinoma cohort, RSF1 was amplified in 16% of the cases. It was correlated with serous histology and a worse prognosis. The 11q13 amplicon in ovarian cancer is likely driven by a cassette of genes rather than by a single oncogene.
- gene copy numbers of EMSY in breast cancers
- Data examine possible allelic imbalance in papillary thyroid cancer at EMSY, CAPN5, and PAK1, as candidate genes within 11q13.5-q14 region using a single nucleotide polymorphism-based analysis.
