PLXNB1-SLC26A6 Fusion FISH Probe
The PLXNB1-SLC26A6 Fusion FISH Probe is used to confirm a fusion of the PLXNB1 and SLC26A6 genes. The fusion of the PLXNB1 and SLC26A6 genes has been associated with Liver Hepatocellular 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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PLXNB1-SLC26A6-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-RERE | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-REOR | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-REGO | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-REGR | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-REAQ | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-ORRE | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-OROR | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-ORGO | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-ORAQ | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-GORE | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-GOOR | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-GOGO | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-GOGR | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-GOAQ | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-GRRE | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-GROR | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-GRGO | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-GRGR | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-GRAQ | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-AQRE | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-AQOR | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-AQGO | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-AQGR | 20 (40 μL) | 200 μL | ||
PLXNB1-SLC26A6-20-AQAQ | 20 (40 μL) | 200 μL |
PLXNB1 Gene Summary
The Plexin B1 (PLXNB1) gene is located on chr3 :48445260-48471460 at 3p21.31.
Gene Name: Plexin B1
Chromosome: CHR3: 48445260 -48471460
Locus: 3p21.31
SLC26A6 Gene Summary
This gene belongs to the solute carrier 26 family, whose members encode anion transporter proteins. This particular family member encodes a protein involved in transporting chloride, oxalate, sulfate and bicarbonate. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Aug 2013]
Gene Name: Solute Carrier Family 26 Member 6
Chromosome: CHR3: 48663155 -48672926
Locus: 3p21.31
Gene Diseases
The PLXNB1 SLC26A6 Fusion has been associated with the following diseases:
Disease Name |
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Liver Hepatocellular Carcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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