SLC52A1 Break Apart FISH Probe
Empire Genomics’ SLC52A1 Break Apart FISH Probe is designed to flank the SLC52A1 gene and is typically used for detecting SLC52A1 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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| SLC52A1BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC52A1BA-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC52A1BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC52A1BA-20-GORE | 20 (40 μL) | 200 μL |
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| SLC52A1BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC52A1BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC52A1BA-20-ORGR | 20 (40 μL) | 200 μL |
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| SLC52A1BA-20-REGO | 20 (40 μL) | 200 μL |
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| SLC52A1BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
Biological redox reactions require electron donors and acceptor. Vitamin B2 is the source for the flavin in flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) which are common redox reagents. This gene encodes a member of the riboflavin (vitamin B2) transporter family. Haploinsufficiency of this protein can cause maternal riboflavin deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jan 2013]
Gene Details
Gene Symbol: SLC52A1
Gene Name: Solute Carrier Family 52 Member 1
Chromosome: CHR17: 5035457-5032601
Locus: 17p13.2
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SLC52A1 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC52A1-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping