SLC35A2 Break Apart FISH Probe
Empire Genomics’ SLC35A2 Break Apart FISH Probe is designed to flank the SLC35A2 gene and is typically used for detecting SLC35A2 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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| SLC35A2BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC35A2BA-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC35A2BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC35A2BA-20-GORE | 20 (40 μL) | 200 μL |
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| SLC35A2BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC35A2BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC35A2BA-20-ORGR | 20 (40 μL) | 200 μL |
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| SLC35A2BA-20-REGO | 20 (40 μL) | 200 μL |
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| SLC35A2BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes a member of the nucleotide-sugar transporter family. The encoded protein is a multi-pass membrane protein. It transports UDP-galactose from the cytosol into Golgi vesicles, where it serves as a glycosyl donor for the generation of glycans. Mutations in this gene cause congenital disorder of glycosylation type IIm (CDG2M). Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Oct 2014]
Gene Details
Gene Symbol: SLC35A2
Gene Name: Solute Carrier Family 35 Member A2
Chromosome: CHRX: 48760458-48768917
Locus: Xp11.23
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SLC35A2 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC35A2-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping