SNX5 Break Apart FISH Probe
Empire Genomics’ SNX5 Break Apart FISH Probe is designed to flank the SNX5 gene and is typically used for detecting SNX5 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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SNX5BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL | ||
SNX5BA-20-AQOR | 20 (40 μL) | 200 μL | ||
SNX5BA-20-GOGR | 20 (40 μL) | 200 μL | ||
SNX5BA-20-GORE | 20 (40 μL) | 200 μL | ||
SNX5BA-20-GRGO | 20 (40 μL) | 200 μL | ||
SNX5BA-20-GRRE | 20 (40 μL) | 200 μL | ||
SNX5BA-20-ORGR | 20 (40 μL) | 200 μL | ||
SNX5BA-20-REGO | 20 (40 μL) | 200 μL | ||
SNX5BA-20-REGR | 20 (40 μL) | 200 μL |
Gene Summary
This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein functions in endosomal sorting, the phosphoinositide-signaling pathway, and macropinocytosis. This gene may play a role in the tumorigenesis of papillary thyroid carcinoma. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2013]
Gene Details
Gene Symbol: SNX5
Gene Name: Sorting Nexin 5
Chromosome: CHR20: 17922243-17949490
Locus: 20p11.23
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SNX5 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SNX5-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping