PrimePCR™ SYBR® Green Assay: TRPM6, 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 qHsaCIP0027501

List Price:    $142.00
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Assay Information

Technology:   qPCR
Assay Type:   SYBR® Green
Application:   Gene Expression
Unique Assay ID:   qHsaCID0010242
Assay Design:   Intron-spanning
Chromosome Location:   9:77457191-77473609question
Amplicon Length:   103
Splice Variants Targeted:   ENST00000360774 ENST00000359047 ENST00000451710 ENST00000376872 ENST00000376871 ENST00000449912 ENST00000361255 ENST00000376870 ENST00000376864 ENST00000448641

Gene Information

This gene is predominantly expressed in the kidney and colon and encodes a protein containing an ion channel domain and a protein kinase domain. It is crucial for magnesium homeostasis and plays an essential role in epithelial magnesium transport and in the active magnesium absorption in the gut and kidney. Mutations in this gene are associated with hypomagnesemia with secondary hypocalcemia. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq Apr 2010]

Gene Symbol:   TRPM6
Gene Name:   transient receptor potential cation channel, subfamily M, member 6
Aliases:   CHAK2, HMGX, HOMG, HOMG1, HSH
RefSeq:   NC_000009.11 NT_008470.19 NG_017036.1
Ensembl:   ENSG00000119121
Entrez:   140803
UniGene:   Hs.272225
Chromosome Mapping:   9q21.13

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 0.998800
y-intercept 34.640000
Efficiency 102

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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