C1QL1-SLC16A5 Fusion FISH Probe
The C1QL1-SLC16A5 Fusion FISH Probe is used to confirm a fusion of the C1QL1 and SLC16A5 genes. The fusion of the C1QL1 and SLC16A5 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.
SKU | Test Kits | Buffer | Dye Color | Order Now |
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C1QL1-SLC16A5-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-RERE | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-REOR | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-REGO | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-REGR | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-REAQ | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-ORRE | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-OROR | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-ORGO | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-ORAQ | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-GORE | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-GOOR | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-GOGO | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-GOGR | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-GOAQ | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-GRRE | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-GROR | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-GRGO | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-GRGR | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-GRAQ | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-AQRE | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-AQOR | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-AQGO | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-AQGR | 20 (40 μL) | 200 μL | ||
C1QL1-SLC16A5-20-AQAQ | 20 (40 μL) | 200 μL |
SLC16A5 Gene Summary
This gene encodes a member of the monocarboxylate transporter family and the major facilitator superfamily. The encoded protein is localized to the cell membrane and acts as a proton-linked transporter of bumetanide. Transport by the encoded protein is inhibited by four loop diuretics, nateglinide, thiazides, probenecid, and glibenclamide. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]
Gene Name: Solute Carrier Family 16 Member 5
Chromosome: CHR17: 73084054 -73102248
Locus: 17q25.1
C1QL1 Gene Summary
The Complement C1q Like 1 (C1QL1) gene is located on chr17 :43037060-43045644 at 17q21.31.
Gene Name: Complement C1q Like 1
Chromosome: CHR17: 43037060 -43045644
Locus: 17q21.31
Gene Diseases
The C1QL1 SLC16A5 Fusion has been associated with the following diseases:
Disease Name |
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Lung Squamous Cell Carcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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