PrimePCR™ Probe Assay: SLC7A7, 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:   qHsaCEP0052941
Assay Design:   exonic
Chromosome Location:   14:23282302-23282442question
Amplicon Length:   111
Splice Variants Targeted:   ENST00000285850 ENST00000555702 ENST00000397532 ENST00000397529 ENST00000397528 ENST00000554758 ENST00000488800 ENST00000555251 ENST00000557629 ENST00000555911 ENST00000557129

Gene Information

The protein encoded by this gene is the light subunit of a cationic amino acid transporter. This sodium-independent transporter is formed when the light subunit encoded by this gene dimerizes with the heavy subunit transporter protein SLC3A2. This transporter is found in epithelial cell membranes where it transfers cationic and large neutral amino acids from the cell to the extracellular space. Defects in this gene are a cause of lysinuric protein intolerance (LPI). Alternative splicing results in multiple transcript variants. [provided by RefSeq Jul 2011]

Gene Symbol:   SLC7A7
Gene Name:   solute carrier family 7 (cationic amino acid transporter, y+ system), member 7
Aliases:   LAT3, LPI, MOP-2, Y+LAT1, y+LAT-1
RefSeq:   NC_000014.8 NT_026437.12 NG_012851.1
Ensembl:   ENSG00000155465
Entrez:   9056
Chromosome Mapping:   14q11.2

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 0.998900
y-intercept 36.240000
Efficiency 95

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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