PrimePCR™ SYBR® Green Assay: RP11-155D18.11, Human

PrimePCR Primer Assays for Real-Time PCR oligo primer pair tube for SYBR Green gene expression

Real-time PCR primer assay designed for SYBR® Green gene expression analysis.

Info:   Same primer pair as used in probe assay qHsaCEP0039794

List Price:    $179.00
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PrimePCR™ PreAmp for SYBR® Green Assay: RP11-155D18.11, Human
Reaction:     400 reactions
Gene-specific PCR primers for the unbiased preamplification of small quantities of cDNA for subsequent use in downstream gene expression analysis.

PrimePCR™ Template for SYBR® Green Assay: RP11-155D18.11, Human
Reaction:     200 x 20 µl reactions desalted
Gene-specific synthetic DNA template designed to give a positive real-time PCR result when used with the corresponding primer assay.


Wet Lab Validated

Assay Information

Technology:   qPCR
Assay Type:   SYBR® Green
Application:   Gene Expression
Unique Assay ID:   qHsaCED0037071
Assay Design:   exonic
Chromosome Location:   3:52023035-52023155question
Amplicon Length:   91
Splice Variants Targeted:   ENST00000340908 ENST00000530271 ENST00000537687 ENST00000315939 ENST00000535572 ENST00000300648 ENST00000534313 ENST00000527525 ENST00000394224 ENST00000394227 ENST00000445101 ENST00000431721 ENST00000446860 ENST00000443964 ENST00000332271 ENST00000263253 ENST00000522555 ENST00000522236 ENST00000316059 ENST00000263801 ENST00000382039 ENST00000382044 ENST00000450115 ENST00000522455 ENST00000518566 ENST00000517638 ENST00000523850 ENST00000521376 ENST00000476854 ENST00000476351 ENST00000494103 ENST

Gene Information

This gene encodes a cytosolic homodimeric zinc-binding enzyme that catalyzes the hydrolysis of acylated L-amino acids to L-amino acids and an acyl group and has been postulated to function in the catabolism and salvage of acylated amino acids. This gene is located on chromosome 3p21.1 a region reduced to homozygosity in small-cell lung cancer (SCLC) and its expression has been reported to be reduced or undetectable in SCLC cell lines and tumors. The amino acid sequence of human aminoacylase-1 is highly homologous to the porcine counterpart and this enzyme is the first member of a new family of zinc-binding enzymes. Mutations in this gene cause aminoacylase-1 deficiency a metabolic disorder characterized by central nervous system defects and increased urinary excretion of N-acetylated amino acids. Alternative splicing of this gene results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ABHD14A (abhydrolase domain containing 14A) gene as represented in GeneID:100526760. A related pseudogene has been identified on chromosome 18. [provided by RefSeq Nov 2010]

Gene Symbol:   RP11-155D18.11
Gene Name:   Aminoacylase-1
Aliases:   ACY-1, ACY1D
RefSeq:   NC_000003.11 NG_012036.1 NT_022517.18
Ensembl:   ENSG00000114786
Entrez:   95
Chromosome Mapping:   3p21.1

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