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CIITA-PRDM16 Fusion FISH Probe

The CIITA-PRDM16 Fusion FISH Probe is used to confirm a fusion of the CIITA and PRDM16 genes. The fusion of the CIITA and PRDM16 genes has been associated with Lymphoid Neoplasm Diffuse Large B-cell Lymphoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.

** This product is for in vitro and research use only. This product is not intended for diagnostic use.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
CIITA-PRDM16-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
CIITA-PRDM16-20-RERE 20 (40 μL) 200 μL
CIITA-PRDM16-20-REOR 20 (40 μL) 200 μL
CIITA-PRDM16-20-REGO 20 (40 μL) 200 μL
CIITA-PRDM16-20-REGR 20 (40 μL) 200 μL
CIITA-PRDM16-20-REAQ 20 (40 μL) 200 μL
CIITA-PRDM16-20-ORRE 20 (40 μL) 200 μL
CIITA-PRDM16-20-OROR 20 (40 μL) 200 μL
CIITA-PRDM16-20-ORGO 20 (40 μL) 200 μL
CIITA-PRDM16-20-ORAQ 20 (40 μL) 200 μL
CIITA-PRDM16-20-GORE 20 (40 μL) 200 μL
CIITA-PRDM16-20-GOOR 20 (40 μL) 200 μL
CIITA-PRDM16-20-GOGO 20 (40 μL) 200 μL
CIITA-PRDM16-20-GOGR 20 (40 μL) 200 μL
CIITA-PRDM16-20-GOAQ 20 (40 μL) 200 μL
CIITA-PRDM16-20-GRRE 20 (40 μL) 200 μL
CIITA-PRDM16-20-GROR 20 (40 μL) 200 μL
CIITA-PRDM16-20-GRGO 20 (40 μL) 200 μL
CIITA-PRDM16-20-GRGR 20 (40 μL) 200 μL
CIITA-PRDM16-20-GRAQ 20 (40 μL) 200 μL
CIITA-PRDM16-20-AQRE 20 (40 μL) 200 μL
CIITA-PRDM16-20-AQOR 20 (40 μL) 200 μL
CIITA-PRDM16-20-AQGO 20 (40 μL) 200 μL
CIITA-PRDM16-20-AQGR 20 (40 μL) 200 μL
CIITA-PRDM16-20-AQAQ 20 (40 μL) 200 μL

CIITA Gene Summary

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. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013]

Gene Name: Class II Major Histocompatibility Complex Transactivator

Chromosome: CHR16: 10971054 -11018840

Locus: 16p13.13

PRDM16 Gene Summary

The reciprocal translocation t(1;3)(p36;q21) occurs in a subset of myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). This gene is located near the 1p36.3 breakpoint and has been shown to be specifically expressed in the t(1:3)(p36,q21)-positive MDS/AML. The protein encoded by this gene is a zinc finger transcription factor and contains an N-terminal PR domain. The translocation results in the overexpression of a truncated version of this protein that lacks the PR domain, which may play an important role in the pathogenesis of MDS and AML. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]

Gene Name: PR/SET Domain 16

Chromosome: CHR1: 2985741 -3355185

Locus: 1p36.32

Gene Diseases

The CIITA PRDM16 Fusion has been associated with the following diseases:

Disease Name
Lymphoid Neoplasm Diffuse Large B-cell Lymphoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.