FAM168A-UVRAG Fusion FISH Probe
The FAM168A-UVRAG Fusion FISH Probe is used to confirm a fusion of the FAM168A and UVRAG genes. The fusion of the FAM168A and UVRAG genes has been associated with Breast Invasive 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.
SKU | Test Kits | Buffer | Dye Color | Order Now |
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FAM168A-UVRAG-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-RERE | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-REOR | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-REGO | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-REGR | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-REAQ | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-ORRE | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-OROR | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-ORGO | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-ORAQ | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-GORE | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-GOOR | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-GOGO | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-GOGR | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-GOAQ | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-GRRE | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-GROR | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-GRGO | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-GRGR | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-GRAQ | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-AQRE | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-AQOR | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-AQGO | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-AQGR | 20 (40 μL) | 200 μL | ||
FAM168A-UVRAG-20-AQAQ | 20 (40 μL) | 200 μL |
UVRAG Gene Summary
This gene complements the ultraviolet sensitivity of xeroderma pigmentosum group C cells and encodes a protein with a C2 domain. The protein activates the Beclin1-PI(3)KC3 complex, promoting autophagy and suppressing the proliferation and tumorigenicity of human colon cancer cells. Chromosomal aberrations involving this gene are associated with left-right axis malformation and mutations in this gene have been associated with colon cancer. [provided by RefSeq, Jul 2008]
Gene Name: UV Radiation Resistance Associated
Chromosome: CHR11: 75526211 -75855282
Locus: 11q13.5
FAM168A Gene Summary
The Family With Sequence Similarity 168 Member A (FAM168A) gene is located on chr11 :73117027-73309228 at 11q13.4.
Gene Name: Family With Sequence Similarity 168 Member A
Chromosome: CHR11: 73117027 -73309228
Locus: 11q13.4
Gene Diseases
The FAM168A UVRAG Fusion has been associated with the following diseases:
Disease Name |
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Breast Invasive Carcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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