SOHLH2 Break Apart FISH Probe
Empire Genomics’ SOHLH2 Break Apart FISH Probe is designed to flank the SOHLH2 gene and is typically used for detecting SOHLH2 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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| SOHLH2BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| SOHLH2BA-20-AQOR | 20 (40 μL) | 200 μL |
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| SOHLH2BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SOHLH2BA-20-GORE | 20 (40 μL) | 200 μL |
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| SOHLH2BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SOHLH2BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SOHLH2BA-20-ORGR | 20 (40 μL) | 200 μL |
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| SOHLH2BA-20-REGO | 20 (40 μL) | 200 μL |
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| SOHLH2BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes one of testis-specific transcription factors which are essential for spermatogenesis, oogenesis and folliculogenesis. This gene is located on chromosome 13. The proteins encoded by this gene and another testis-specific transcription factor, SOHLH1, can form heterodimers, in addition to homodimers. There is a read-through locus (GeneID: 100526761) that shares sequence identity with this gene and the upstream CCDC169 (GeneID: 728591). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]
Gene Details
Gene Symbol: SOHLH2
Gene Name: Spermatogenesis And Oogenesis Specific Basic Helix-loop-helix 2
Chromosome: CHR13: 36742344-36788752
Locus: 13q13.3
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SOHLH2 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SOHLH2-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping