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CNBP-ALDH1L1 Fusion FISH Probe

The CNBP-ALDH1L1 Fusion FISH Probe is used to confirm a fusion of the CNBP and ALDH1L1 genes. The fusion of the CNBP and ALDH1L1 genes has been associated with Brain Lower Grade Glioma. 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.

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

SKU Test Kits Buffer Dye Color Order Now
CNBP-ALDH1L1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-RERE 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-REOR 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-REGO 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-REGR 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-REAQ 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-ORRE 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-OROR 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-ORGO 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-ORAQ 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-GORE 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-GOOR 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-GOGO 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-GOGR 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-GOAQ 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-GRRE 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-GROR 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-GRGO 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-GRGR 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-GRAQ 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-AQRE 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-AQOR 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-AQGO 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-AQGR 20 (40 μL) 200 μL
CNBP-ALDH1L1-20-AQAQ 20 (40 μL) 200 μL

CNBP Gene Summary

This gene encodes a nucleic-acid binding protein with seven zinc-finger domains. The protein has a preference for binding single stranded DNA and RNA. The protein functions in cap-independent translation of ornithine decarboxylase mRNA, and may also function in sterol-mediated transcriptional regulation. A CCTG expansion from <30 repeats to 75-11000 repeats in the first intron of this gene results in myotonic dystrophy type 2. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2016]

Gene Name: CCHC-type Zinc Finger Nucleic Acid Binding Protein

Chromosome: CHR3: 128886657 -128902810

Locus: 3q21.3

ALDH1L1 Gene Summary

The protein encoded by this gene catalyzes the conversion of 10-formyltetrahydrofolate, nicotinamide adenine dinucleotide phosphate (NADP+), and water to tetrahydrofolate, NADPH, and carbon dioxide. The encoded protein belongs to the aldehyde dehydrogenase family. Loss of function or expression of this gene is associated with decreased apoptosis, increased cell motility, and cancer progression. There is an antisense transcript that overlaps on the opposite strand with this gene locus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]

Gene Name: Aldehyde Dehydrogenase 1 Family Member L1

Chromosome: CHR3: 125822407 -125899485

Locus: 3q21.3

Gene Diseases

The CNBP ALDH1L1 Fusion has been associated with the following diseases:

Disease Name
Brain Lower Grade Glioma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.