PrimePCR™ ddPCR™ Expression Probe Assay: FANCA, Human

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PrimePCR Primer Assays for Real-Time PCR oligo primer pair tube for SYBR Green gene expression

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

Info:   HEX; Same primer pair and probe as used in qPCR assay qHsaCIP0031497; Intron-spanning

 
Fluorophore:   HEX
List Price:    $195.00
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Assay Information

Technology:   ddPCR
Assay Type:   Probe
Application:   Gene Expression
Unique Assay ID:   dHsaCPE5056149
Chromosome Location:   16:89880938-89882379question
Amplicon Length:   149

Gene Information

The Fanconi anemia complementation group (FANC) currently includes FANCA FANCB FANCC FANCD1 (also called BRCA2) FANCD2 FANCE FANCF FANCG FANCI FANCJ (also called BRIP1) FANCL FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability hypersensitivity to DNA crosslinking agents increased chromosomal breakage and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group A. Alternative splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are the most common cause of Fanconi anemia. [provided by RefSeq Jul 2008]

Gene Symbol:   FANCA
Gene Name:   Fanconi anemia, complementation group A
Aliases:   FA, FA-H, FA1, FAA, FACA, FAH, FANCH, MGC75158
RefSeq:   NC_000016.9 NG_011706.1 NT_010542.15
Ensembl:   ENSG00000187741
Entrez:   2175
UniGene:   Hs.290154
Chromosome Mapping:   16q24.3

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