PKM2-SLC1A3 Fusion FISH Probe
The PKM2-SLC1A3 Fusion FISH Probe is used to confirm a fusion of the PKM2 and SLC1A3 genes. The fusion of the PKM2 and SLC1A3 genes has been associated with Brain Lower Grade Glioma. 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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PKM2-SLC1A3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-RERE | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-REOR | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-REGO | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-REGR | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-REAQ | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-ORRE | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-OROR | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-ORGO | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-ORAQ | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-GORE | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-GOOR | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-GOGO | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-GOGR | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-GOAQ | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-GRRE | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-GROR | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-GRGO | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-GRGR | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-GRAQ | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-AQRE | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-AQOR | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-AQGO | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-AQGR | 20 (40 μL) | 200 μL | ||
PKM2-SLC1A3-20-AQAQ | 20 (40 μL) | 200 μL |
SLC1A3 Gene Summary
This gene encodes a member of a member of a high affinity glutamate transporter family. This gene functions in the termination of excitatory neurotransmission in central nervous system. Mutations are associated with episodic ataxia, Type 6. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2014]
Gene Name: Solute Carrier Family 1 Member 3
Chromosome: CHR5: 36606456 -36688436
Locus: 5p13.2
Gene Diseases
The PKM2 SLC1A3 Fusion has been associated with the following diseases:
Disease Name |
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Brain Lower Grade Glioma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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