PrimePCR™ SYBR® Green Assay: SENP1, 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:   Recommended - best coverage; Same primer pair as used in probe assay qHsaCEP0049701

List Price:    $146.00
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Assay Information

Technology:   qPCR
Assay Type:   SYBR® Green
Application:   Gene Expression
Unique Assay ID:   qHsaCED0042439
Assay Design:   exonic
Chromosome Location:   12:48477517-48482658question
Amplicon Length:   74
Splice Variants Targeted:   ENST00000551330 ENST00000549595 ENST00000549518 ENST00000551798 ENST00000004980 ENST00000448372 ENST00000339976

Gene Information

The covalent modification of proteins by the small ubiquitin (UBB; MIM 191339)-like protein SUMO (see SUMO1 MIM 601912) is implicated in the regulation of nucleocytoplasmic transport genomic stability gene transcription and other processes. Sumoylation is catalyzed on target lysine residues by a multienzyme process and is reversed by desumoylating enzymes such as SENP1 (Yamaguchi et al. 2005 [PubMed 15923632]).[supplied by OMIM Jul 2008]

Gene Symbol:   SENP1
Gene Name:   SUMO1/sentrin specific peptidase 1
Aliases:   SuPr-2
RefSeq:   NG_016199.1 NC_000012.11 NT_029419.12
Ensembl:   ENSG00000079387
Entrez:   29843
UniGene:   Hs.371957
Chromosome Mapping:   12q13.1

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™ Universal SYBR® Green Supermix
Experimental Sample qPCR Human Reference Total RNA

Summary Data:

R2 0.999800
y-intercept 35.730000
Efficiency 99

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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