SLC7A14 Break Apart FISH Probe
Empire Genomics’ SLC7A14 Break Apart FISH Probe is designed to flank the SLC7A14 gene and is typically used for detecting SLC7A14 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in green and orange 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 |
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SLC7A14BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL | ||
SLC7A14BA-20-AQOR | 20 (40 μL) | 200 μL | ||
SLC7A14BA-20-GOGR | 20 (40 μL) | 200 μL | ||
SLC7A14BA-20-GORE | 20 (40 μL) | 200 μL | ||
SLC7A14BA-20-GRGO | 20 (40 μL) | 200 μL | ||
SLC7A14BA-20-GRRE | 20 (40 μL) | 200 μL | ||
SLC7A14BA-20-ORGR | 20 (40 μL) | 200 μL | ||
SLC7A14BA-20-REGO | 20 (40 μL) | 200 μL | ||
SLC7A14BA-20-REGR | 20 (40 μL) | 200 μL |
Gene Summary
This gene is predicted to encode a glycosylated, cationic amino acid transporter protein with 14 transmembrane domains. This gene is primarily expressed in skin fibroblasts, neural tissue, and primary endothelial cells and its protein is predicted to mediate lysosomal uptake of cationic amino acids. Mutations in this gene are associated with autosomal recessive retinitis pigmentosa. In mice, this gene is expressed in the photoreceptor layer of the retina where its expression increases over the course of retinal development and persists in the mature retina. [provided by RefSeq, Apr 2014]
Gene Details
Gene Symbol: SLC7A14
Gene Name: Solute Carrier Family 7 Member 14
Chromosome: CHR3: 170177341-170303863
Locus: 3q26.2
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SLC7A14 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC7A14-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping