PrimePCR™ Probe Assay: NAT6, 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.

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Assay Information

Technology:   qPCR
Assay Type:   Probe
Application:   Gene Expression
Unique Assay ID:   qHsaCEP0041161
Assay Design:   exonic
Chromosome Location:   3:50334731-50334823question
Amplicon Length:   63
Splice Variants Targeted:   ENST00000571600 ENST00000577007 ENST00000573208 ENST00000575928 ENST00000570345 ENST00000571097 ENST00000354862 ENST00000417393 ENST00000443094 ENST00000443842 ENST00000450489 ENST00000442620

Gene Information

This gene encodes a member of the N-acetyltransferase family. N-acetyltransferases modify proteins by transferring acetyl groups from acetyl CoA to the N-termini of protein substrates. The encoded protein is a cytoplasmic N-acetyltransferase with a substrate specificity for proteins with an N-terminal methionine. This gene is located in the tumor suppressor gene region on chromosome 3p21.3 and the encoded protein may play a role in cancer. Alternatively spliced transcript variants encoding multiple isoforms have been observed. This gene overlaps and is on the same strand as hyaluronoglucosaminidase 3 and some transcripts of each gene share a portion of the first exon. [provided by RefSeq Jan 2011]

Gene Symbol:   NAT6
Gene Name:   N-acetyltransferase 6 (GCN5-related)
Aliases:   FUS-2, FUS2
RefSeq:   NG_009295.1 NC_000003.11 NT_022517.18
Ensembl:   ENSG00000243477
Entrez:   24142
Chromosome Mapping:   3p21.3

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 0.999200
y-intercept 36.090000
Efficiency 97

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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