PrimePCR™ Probe Assay: TFPI, 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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PrimePCR™ PreAmp for Probe Assay: TFPI, Human
Reaction:     400 reactions
Gene-specific PCR primers for the unbiased preamplification of small quantities of cDNA for subsequent use in downstream gene expression analysis.

PrimePCR™ Template for Probe Assay: TFPI, Human
Reaction:     200 x 20 µl reactions
Gene-specific synthetic DNA template designed to give a positive real-time PCR result when used with the corresponding probe assay.


Wet Lab Validated

Assay Information

Technology:   qPCR
Assay Type:   Probe
Application:   Gene Expression
Unique Assay ID:   qHsaCIP0033673
Assay Design:   Intron-spanning
Chromosome Location:   2:188361768-188368464question
Amplicon Length:   98
Splice Variants Targeted:   ENST00000392365 ENST00000426055 ENST00000435414 ENST00000409676 ENST00000339091 ENST00000437725 ENST00000421427 ENST00000453013 ENST00000417013 ENST00000420747 ENST00000233156

Gene Information

This gene encodes a protease inhibitor that regulates the tissue factor (TF)-dependent pathway of blood coagulation. The coagulation process initiates with the formation of a factor VIIa-TF complex which proteolytically activates additional proteases (factors IX and X) and ultimately leads to the formation of a fibrin clot. The product of this gene inhibits the activated factor X and VIIa-TF proteases in an autoregulatory loop. The encoded protein is glycosylated and predominantly found in the vascular endothelium and plasma in both free forms and complexed with plasma lipoproteins. Several alternatively spliced transcript variants of this gene have been described but the full-length nature of some of these variants has not been confirmed. [provided by RefSeq Jul 2008]

Gene Symbol:   TFPI
Gene Name:   tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor)
Aliases:   EPI, LACI, TFI, TFPI1
RefSeq:   NC_000002.11 NT_005403.17
Ensembl:   ENSG00000003436
Entrez:   7035
Chromosome Mapping:   2q32

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