SLC35D1 Break Apart FISH Probe
Empire Genomics’ SLC35D1 Break Apart FISH Probe is designed to flank the SLC35D1 gene and is typically used for detecting SLC35D1 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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| SLC35D1BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC35D1BA-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC35D1BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC35D1BA-20-GORE | 20 (40 μL) | 200 μL |
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| SLC35D1BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC35D1BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC35D1BA-20-ORGR | 20 (40 μL) | 200 μL |
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| SLC35D1BA-20-REGO | 20 (40 μL) | 200 μL |
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| SLC35D1BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
Glycosylation of cellular glycoconjugates occurs in the endoplasmic reticulum (ER) and Golgi compartment, and requires transport of nucleotide sugars from the cytosol into the lumen of the ER and Golgi by specific transporters. The protein encoded by this gene resides in the ER, and transports both UDP-glucuronic acid (UDP-GlcA) and UDP-N-acetylgalactosamine (UDP-GalNAc) from the cytoplasm to the ER lumen. It may participate in glucuronidation and/or chondroitin sulfate biosynthesis. Mutations in this gene are associated with Schneckenbecken dysplasia.[provided by RefSeq, Sep 2009]
Gene Details
Gene Symbol: SLC35D1
Gene Name: Solute Carrier Family 35 Member D1
Chromosome: CHR1: 67465014-67520080
Locus: 1p31.3
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SLC35D1 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC35D1-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping