PrimePCR™ ddPCR™ Expression Probe Assay: SLC16A2, Human


ddPCR probe assay designed for gene expression analysis. Probe assays consist of unlabeled PCR primers and a dual labeled fluorescent probe.

Info:   FAM; Same primer pair and probe as used in qPCR assay qHsaCIP0030081; Intron-spanning

Fluorophore:   FAM
List Price:    $207.00
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Assay Information

Technology:   ddPCR
Assay Type:   Probe
Application:   Gene Expression
Unique Assay ID:   dHsaCPE5053490
Chromosome Location:   X:73740856-73744258question
Amplicon Length:   149

Gene Information

This gene encodes an integral membrane protein that functions as a transporter of thyroid hormone. The encoded protein facilitates the cellular importation of thyroxine (T4) triiodothyronine (T3) reverse triiodothyronine (rT3) and diidothyronine (T2). This gene is expressed in many tissues and likely plays an important role in the development of the central nervous system. Loss of function mutations in this gene are associated with psychomotor retardation in males while females exhibit no neurological defects and more moderate thyroid-deficient phenotypes. This gene is subject to X-chromosome inactivation. Mutations in this gene are the cause of Allan-Herndon-Dudley syndrome. [provided by RefSeq Mar 2012]

Gene Symbol:   SLC16A2
Gene Name:   solute carrier family 16, member 2 (monocarboxylic acid transporter 8)
Aliases:   AHDS, DXS128, DXS128E, MCT 7, MCT 8, MCT7, MCT8, MRX22, XPCT
RefSeq:   NC_000023.10 NG_011641.1 NT_011669.17
Ensembl:   ENSG00000147100
Entrez:   6567
UniGene:   Hs.75317
Chromosome Mapping:   Xq13.2

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