TTC8 Break Apart FISH Probe
Empire Genomics’ TTC8 Break Apart FISH Probe is designed to flank the TTC8 gene and is typically used for detecting TTC8 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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| TTC8BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| TTC8BA-20-AQOR | 20 (40 μL) | 200 μL |
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| TTC8BA-20-GOGR | 20 (40 μL) | 200 μL |
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| TTC8BA-20-GORE | 20 (40 μL) | 200 μL |
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| TTC8BA-20-GRGO | 20 (40 μL) | 200 μL |
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| TTC8BA-20-GROR | 20 (40 μL) | 200 μL |
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| TTC8BA-20-GRRE | 20 (40 μL) | 200 μL |
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| TTC8BA-20-REGO | 20 (40 μL) | 200 μL |
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| TTC8BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is involved in the formation of cilia. A mutation in this gene has also been implicated in nonsyndromic retinitis pigmentosa. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]
Gene Details
Gene Symbol: TTC8
Gene Name: Tetratricopeptide Repeat Domain 8
Chromosome: CHR14: 89290977-89344335
Locus: 14q31.3
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: TTC8 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: TTC8-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping