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PDXP-SLC17A9 Fusion FISH Probe

The PDXP-SLC17A9 Fusion FISH Probe is used to confirm a fusion of the PDXP and SLC17A9 genes. The fusion of the PDXP and SLC17A9 genes has been associated with Bladder Urothelial 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.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
PDXP-SLC17A9-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
PDXP-SLC17A9-20-RERE 20 (40 μL) 200 μL
PDXP-SLC17A9-20-REOR 20 (40 μL) 200 μL
PDXP-SLC17A9-20-REGO 20 (40 μL) 200 μL
PDXP-SLC17A9-20-REGR 20 (40 μL) 200 μL
PDXP-SLC17A9-20-REAQ 20 (40 μL) 200 μL
PDXP-SLC17A9-20-ORRE 20 (40 μL) 200 μL
PDXP-SLC17A9-20-OROR 20 (40 μL) 200 μL
PDXP-SLC17A9-20-ORGO 20 (40 μL) 200 μL
PDXP-SLC17A9-20-ORAQ 20 (40 μL) 200 μL
PDXP-SLC17A9-20-GORE 20 (40 μL) 200 μL
PDXP-SLC17A9-20-GOOR 20 (40 μL) 200 μL
PDXP-SLC17A9-20-GOGO 20 (40 μL) 200 μL
PDXP-SLC17A9-20-GOGR 20 (40 μL) 200 μL
PDXP-SLC17A9-20-GOAQ 20 (40 μL) 200 μL
PDXP-SLC17A9-20-GRRE 20 (40 μL) 200 μL
PDXP-SLC17A9-20-GROR 20 (40 μL) 200 μL
PDXP-SLC17A9-20-GRGO 20 (40 μL) 200 μL
PDXP-SLC17A9-20-GRGR 20 (40 μL) 200 μL
PDXP-SLC17A9-20-GRAQ 20 (40 μL) 200 μL
PDXP-SLC17A9-20-AQRE 20 (40 μL) 200 μL
PDXP-SLC17A9-20-AQOR 20 (40 μL) 200 μL
PDXP-SLC17A9-20-AQGO 20 (40 μL) 200 μL
PDXP-SLC17A9-20-AQGR 20 (40 μL) 200 μL
PDXP-SLC17A9-20-AQAQ 20 (40 μL) 200 μL

PDXP Gene Summary

Pyridoxal 5-prime-phosphate (PLP) is the active form of vitamin B6 that acts as a coenzyme in maintaining biochemical homeostasis. The preferred degradation route from PLP to 4-pyridoxic acid involves the dephosphorylation of PLP by PDXP (Jang et al., 2003 [PubMed 14522954]).[supplied by OMIM, Mar 2008]

Gene Name: Pyridoxal Phosphatase

Chromosome: CHR22: 38054736 -38062939

Locus: 22q13.1

SLC17A9 Gene Summary

This gene encodes a member of a family of transmembrane proteins that are involved in the transport of small molecules. The encoded protein participates in the vesicular uptake, storage, and secretion of adenoside triphosphate (ATP) and other nucleotides. A mutation in this gene was found in individuals with autosomal dominant disseminated superficial actinic porokeratosis-8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]

Gene Name: Solute Carrier Family 17 Member 9

Chromosome: CHR20: 61583998 -61599949

Locus: 20q13.33

Gene Diseases

The PDXP SLC17A9 Fusion has been associated with the following diseases:

Disease Name
Bladder Urothelial Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.