SLC35A4-PEX1 Fusion FISH Probe
The SLC35A4-PEX1 Fusion FISH Probe is used to confirm a fusion of the SLC35A4 and PEX1 genes. The fusion of the SLC35A4 and PEX1 genes has been associated with Kidney Renal Papillary 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| SLC35A4-PEX1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-RERE | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-REOR | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-REGO | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-REGR | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-REAQ | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-ORRE | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-OROR | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-ORGO | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-ORAQ | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-GORE | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-GOOR | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-GOGO | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-GOAQ | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-GROR | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-GRGR | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-GRAQ | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-AQRE | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-AQGO | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-AQGR | 20 (40 μL) | 200 μL |
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| SLC35A4-PEX1-20-AQAQ | 20 (40 μL) | 200 μL |
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PEX1 Gene Summary
This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2013]
Gene Name: Peroxisomal Biogenesis Factor 1
Chromosome: CHR7: 92116336 -92157845
Locus: 7q21.2
SLC35A4 Gene Summary
The Solute Carrier Family 35 Member A4 (SLC35A4) gene is located on chr5 :139944419-139948683 at 5q31.3.
Gene Name: Solute Carrier Family 35 Member A4
Chromosome: CHR5: 139944419 -139948683
Locus: 5q31.3
Gene Diseases
The SLC35A4 PEX1 Fusion has been associated with the following diseases:
| Disease Name |
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| Kidney Renal Papillary Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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