PrimePCR™ Probe Assay: GTPBP4, 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:   qHsaCIP0032902
Assay Design:   Intron-spanning
Chromosome Location:   10:1042107-1044947question
Amplicon Length:   151
Splice Variants Targeted:   ENST00000360803 ENST00000360059 ENST00000545048 ENST00000538293

Gene Information

GTP-binding proteins are GTPases and function as molecular switches that can flip between two states: active when GTP is bound and inactive when GDP is bound. 'Active' in this context usually means that the molecule acts as a signal to trigger other events in the cell. When an extracellular ligand binds to a G-protein-linked receptor the receptor changes its conformation and switches on the trimeric G proteins that associate with it by causing them to eject their GDP and replace it with GTP. The switch is turned off when the G protein hydrolyzes its own bound GTP converting it back to GDP. But before that occurs the active protein has an opportunity to diffuse away from the receptor and deliver its message for a prolonged period to its downstream target. [provided by RefSeq Jul 2008]

Gene Symbol:   GTPBP4
Gene Name:   GTP binding protein 4
Aliases:   CRFG, FLJ10686, FLJ10690, FLJ39774, NGB, NOG1
RefSeq:   NC_000010.10 NT_008705.16
Ensembl:   ENSG00000107937
Entrez:   23560
Chromosome Mapping:   10p15-p14

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 0.999500
y-intercept 34.900000
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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