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C3ORF55-CHRD Fusion FISH Probe

The C3ORF55-CHRD Fusion FISH Probe is used to confirm a fusion of the C3ORF55 and CHRD genes. The fusion of the C3ORF55 and CHRD genes has been associated with Lung Squamous Cell Carcinoma. 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
C3ORF55-CHRD-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
C3ORF55-CHRD-20-RERE 20 (40 μL) 200 μL
C3ORF55-CHRD-20-REOR 20 (40 μL) 200 μL
C3ORF55-CHRD-20-REGO 20 (40 μL) 200 μL
C3ORF55-CHRD-20-REGR 20 (40 μL) 200 μL
C3ORF55-CHRD-20-REAQ 20 (40 μL) 200 μL
C3ORF55-CHRD-20-ORRE 20 (40 μL) 200 μL
C3ORF55-CHRD-20-OROR 20 (40 μL) 200 μL
C3ORF55-CHRD-20-ORGO 20 (40 μL) 200 μL
C3ORF55-CHRD-20-ORAQ 20 (40 μL) 200 μL
C3ORF55-CHRD-20-GORE 20 (40 μL) 200 μL
C3ORF55-CHRD-20-GOOR 20 (40 μL) 200 μL
C3ORF55-CHRD-20-GOGO 20 (40 μL) 200 μL
C3ORF55-CHRD-20-GOGR 20 (40 μL) 200 μL
C3ORF55-CHRD-20-GOAQ 20 (40 μL) 200 μL
C3ORF55-CHRD-20-GRRE 20 (40 μL) 200 μL
C3ORF55-CHRD-20-GROR 20 (40 μL) 200 μL
C3ORF55-CHRD-20-GRGO 20 (40 μL) 200 μL
C3ORF55-CHRD-20-GRGR 20 (40 μL) 200 μL
C3ORF55-CHRD-20-GRAQ 20 (40 μL) 200 μL
C3ORF55-CHRD-20-AQRE 20 (40 μL) 200 μL
C3ORF55-CHRD-20-AQOR 20 (40 μL) 200 μL
C3ORF55-CHRD-20-AQGO 20 (40 μL) 200 μL
C3ORF55-CHRD-20-AQGR 20 (40 μL) 200 μL
C3ORF55-CHRD-20-AQAQ 20 (40 μL) 200 μL

CHRD Gene Summary

This gene encodes a secreted protein that dorsalizes early vertebrate embryonic tissues by binding to ventralizing TGF-beta-like bone morphogenetic proteins and sequestering them in latent complexes. The encoded protein may also have roles in organogenesis and during adulthood. It has been suggested that this gene could be a candidate gene for Cornelia de Lange syndrome. Reduced expression of this gene results in enhanced bone regeneration. Alternative splicing results in multiple transcript variants. Other alternative splice variants have been described but their full length sequence has not been determined. [provided by RefSeq, Jan 2015]

Gene Name: Chordin

Chromosome: CHR3: 184097860 -184107617

Locus: 3q27.1

Gene Diseases

The C3ORF55 CHRD Fusion has been associated with the following diseases:

Disease Name
Lung Squamous Cell Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.