SRD5A3 Break Apart FISH Probe
Empire Genomics’ SRD5A3 Break Apart FISH Probe is designed to flank the SRD5A3 gene and is typically used for detecting SRD5A3 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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| SRD5A3BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SRD5A3BA-20-AQOR | 20 (40 μL) | 200 μL |
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| SRD5A3BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SRD5A3BA-20-GORE | 20 (40 μL) | 200 μL |
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| SRD5A3BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SRD5A3BA-20-GROR | 20 (40 μL) | 200 μL |
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| SRD5A3BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SRD5A3BA-20-REGO | 20 (40 μL) | 200 μL |
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| SRD5A3BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
The protein encoded by this gene belongs to the steroid 5-alpha reductase family, and polyprenol reductase subfamily. It is involved in the production of androgen 5-alpha-dihydrotestosterone (DHT) from testosterone, and maintenance of the androgen-androgen receptor activation pathway. This protein is also necessary for the conversion of polyprenol into dolichol, which is required for the synthesis of dolichol-linked monosaccharides and the oligosaccharide precursor used for N-linked glycosylation of proteins. Mutations in this gene are associated with congenital disorder of glycosylation type Iq. [provided by RefSeq, Mar 2011]
Gene Details
Gene Symbol: SRD5A3
Gene Name: Steroid 5 Alpha-reductase 3
Chromosome: CHR4: 56212387-56239266
Locus: 4q12
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SRD5A3 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SRD5A3-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping