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Validated All-in-One™ qPCR Primer for LMO3(NM_001243611.1) Search again
Product ID:
HQP059149
(click here to view gene annotation page)
Powered by BiozSpecies:
Human
Symbol:
Alias:
RBTN3, RBTNL2, RHOM3, Rhom-3
Gene Description:
LIM domain only 3
Target Gene Accession:
NM_001243611.1(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 deregulated expression of neuronal-specific LMO3 and HEN2 contributes to the genesis and progression of human neuroblastoma in a lineage-specific manner.
- The current findings have implications for treatment response to drugs currently in use (or being developed) for the treatment of overeating and overweight.
- This study found that SNP rs463379 was significantly associated with ADHD.
- did not demonstrate a significant association between methylphenidate treatment response and the polymorphisms DRD4 VNTR, CHRNA4 (rs1044396 and rs6090384) and the long (L(A) and L(G)) and short (S) forms of the serotonin transporter promoter region
- Analyses revealed that two of the three polymorphisms (i.e., His452Tyr and DAT1) were associated with adolescent ASB.
- Evidence for association between hyperactive-impulsive ADHD symptoms and DAT1 and between inattentive ADHD symptoms and DRD4.