PrimePCR™ Probe Assay: IMPDH1, Human

RT

Real-time PCR probe assay designed for gene expression analysis. Probe assays consist of unlabeled PCR primers and a dual labeled fluorescent probe.

List Price:    $255.00
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Assay Information

Technology:   qPCR
Assay Type:   Probe
Application:   Gene Expression
Unique Assay ID:   qHsaCIP0040696
Assay Design:   Intron-spanning
Chromosome Location:   7:128037014-128038536question
Amplicon Length:   102
Splice Variants Targeted:   ENST00000419067 ENST00000338791 ENST00000496200 ENST00000354269 ENST00000348127 ENST00000470772 ENST00000480861 ENST00000378717 ENST00000343214 ENST00000395148

Gene Information

The protein encoded by this gene acts as a homotetramer to regulate cell growth. The encoded protein is an enzyme that catalyzes the synthesis of xanthine monophosphate (XMP) from inosine-5'-monophosphate (IMP). This is the rate-limiting step in the de novo synthesis of guanine nucleotides. Defects in this gene are a cause of retinitis pigmentosa type 10 (RP10). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq Dec 2008]

Gene Symbol:   IMPDH1
Gene Name:   IMP (inosine 5'-monophosphate) dehydrogenase 1
Aliases:   DKFZp781N0678, IMPD, IMPD1, LCA11, RP10, sWSS2608
RefSeq:   NC_000007.13 NG_009194.1 NT_007933.15
Ensembl:   ENSG00000106348
Entrez:   3614
Chromosome Mapping:   7q31.3-q32

The below validation information is for the Primer Pair only   Download Validation Data (.pdf)


Products used to generate validation data:

Real-Time PCR Instrument CFX384 Real-Time PCR Detection System
Reverse Transcription Reagent iScript™ Advanced cDNA Synthesis Kit for RT-qPCR
Real-Time PCR Supermix SsoAdvanced™ SYBR® Green Supermix
Experimental Sample qPCR Human Reference Total RNA

Summary Data:

R2 0.999300
y-intercept 35.690000
Efficiency 98

Amplification Plot
Amplification of cDNA generated from universal RNA.

Amplification of cDNA generated from universal RNA.

Melt Peak
Melt curve analysis of above amplification.

Melt curve analysis of above amplification.

Standard Curve
Standard curve generated using 20 million copies of template diluted 10 fold to 20 copies.

Standard curve generated using 20 million copies of template diluted 10 fold to 20 copies.

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