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Validated All-in-One™ qPCR Primer for HUWE1(NM_031407.6) Search again
Product ID:
HQP000096
(click here to view gene annotation page)
Species:
Human
Symbol:
Alias:
ARF-BP1, HECTH9, HSPC272, Ib772, LASU1, MRXST, MULE, URE-B1, UREB1
Gene Description:
HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1
Target Gene Accession:
NM_031407.6(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.
Validated result:
Gene References into function
- Ubiquitin ligase activity of ARF-BP1 (HUWE1) is inhibited by Arf.
- study modifies the current view of ARF-mediated p53 activation and reveals that ARF-BP1 is a critical mediator of both the p53-independent and p53-dependent tumor suppressor functions of ARF
- Mule (HUWE1) poly-ubiquitinates anti-apoptotic gene Mcl-1.
- Mule is both required and sufficient for the polyubiquitination of Mcl-1; Mule is a unique BH3-containing E3 ubiquitin ligase apical to Bcl-2 family proteins during DNA damage-induced apoptosis
- LASU1 is an E3 ligase that ubiquitinates Mcl-1 in vitro and is required for its proteasome-dependent degradation, the BH3 domain of LASU1 interactes with Mcl-1.
- HectH9-mediated ubiquitination of Myc is required for transactivation of multiple target genes.
- These findings demonstrate an important and conserved role for Huwe1 in regulating Cdc6 abundance after DNA damage.
- An increased gene dosage of HSD17B10, HUWE1, or both contribute to the etiology of X-Linked Mental Retardation and suggest that point mutations in HUWE1 are associated with this disease too.
- Huwe1 links destruction of N-Myc to the quiescent state that complements differentiation in the neural tissue
- Miz1 and Myc affect the activity of the Atr checkpoint through their effect on TopBP1 chromatin association and stability.
