SLC35A1 Break Apart FISH Probe
Empire Genomics’ SLC35A1 Break Apart FISH Probe is designed to flank the SLC35A1 gene and is typically used for detecting SLC35A1 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 |
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| SLC35A1BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC35A1BA-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC35A1BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC35A1BA-20-GORE | 20 (40 μL) | 200 μL |
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| SLC35A1BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC35A1BA-20-GROR | 20 (40 μL) | 200 μL |
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| SLC35A1BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC35A1BA-20-REGO | 20 (40 μL) | 200 μL |
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| SLC35A1BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
The protein encoded by this gene is found in the membrane of the Golgi apparatus, where it transports nucleotide sugars into the Golgi. One such nucleotide sugar is CMP-sialic acid, which is imported into the Golgi by the encoded protein and subsequently glycosylated. Defects in this gene are a cause of congenital disorder of glycosylation type 2F (CDG2F). Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Dec 2009]
Gene Details
Gene Symbol: SLC35A1
Gene Name: Solute Carrier Family 35 Member A1
Chromosome: CHR6: 88182642-88222057
Locus: 6q15
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SLC35A1 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC35A1-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping