SLC6A17 Break Apart FISH Probe
Empire Genomics’ SLC6A17 Break Apart FISH Probe is designed to flank the SLC6A17 gene and is typically used for detecting SLC6A17 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in orange and green by default, but may be customized to meet your needs.
** 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 |
---|---|---|---|---|
SLC6A17BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
SLC6A17BA-20-AQOR | 20 (40 μL) | 200 μL | ||
SLC6A17BA-20-GOGR | 20 (40 μL) | 200 μL | ||
SLC6A17BA-20-GORE | 20 (40 μL) | 200 μL | ||
SLC6A17BA-20-GRGO | 20 (40 μL) | 200 μL | ||
SLC6A17BA-20-GROR | 20 (40 μL) | 200 μL | ||
SLC6A17BA-20-GRRE | 20 (40 μL) | 200 μL | ||
SLC6A17BA-20-REGO | 20 (40 μL) | 200 μL | ||
SLC6A17BA-20-REGR | 20 (40 μL) | 200 μL |
Gene Summary
The protein encoded by this gene is a member of the SLC6 family of transporters, which are responsible for the presynaptic uptake of most neurotransmitters. The encoded vesicular transporter is selective for proline, glycine, leucine and alanine. In mouse, the strongest expression of this gene was in cortical and hippocampal tissues where expression increased during embryonic brain development and peaked postnatally. Defects in this gene cause a form of autosomal recessive intellectual disability. [provided by RefSeq, Jul 2017]
Gene Details
Gene Symbol: SLC6A17
Gene Name: Solute Carrier Family 6 Member 17
Chromosome: CHR1: 110693131-110744823
Locus: 1p13.3
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SLC6A17 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC6A17-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping