PrimePCR™ Probe Assay: CIITA, 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: CIITA, 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: CIITA, 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:   qHsaCIP0029590
Assay Design:   Intron-spanning
Chromosome Location:   16:11017139-11017786question
Amplicon Length:   66
Splice Variants Targeted:   ENST00000324288 ENST00000381835

Gene Information

This gene encodes a protein with an acidic transcriptional activation domain 4 LRRs (leucine-rich repeats) and a GTP binding domain. The protein is located in the nucleus and acts as a positive regulator of class II major histocompatibility complex gene transcription and is referred to as the "master control factor" for the expression of these genes. The protein also binds GTP and uses GTP binding to facilitate its own transport into the nucleus. Once in the nucleus it does not bind DNA but rather uses an intrinsic acetyltransferase (AT) activity to act in a coactivator-like fashion. Mutations in this gene have been associated with bare lymphocyte syndrome type II (also known as hereditary MHC class II deficiency or HLA class II-deficient combined immunodeficiency) increased susceptibility to rheumatoid arthritis multiple sclerosis and possibly myocardial infarction. [provided by RefSeq Jul 2008]

Gene Symbol:   CIITA
Gene Name:   class II, major histocompatibility complex, transactivator
Aliases:   C2TA, CIITAIV, MHC2TA, NLRA
RefSeq:   NC_000016.9 NG_009628.1 NT_010393.16
Ensembl:   ENSG00000179583
Entrez:   4261
Chromosome Mapping:   16p13

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