KCTD17 Break Apart FISH Probe
Empire Genomics’ KCTD17 Break Apart FISH Probe is designed to flank the KCTD17 gene and is typically used for detecting KCTD17 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 |
---|---|---|---|---|
KCTD17BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
KCTD17BA-20-AQOR | 20 (40 μL) | 200 μL | ||
KCTD17BA-20-GOGR | 20 (40 μL) | 200 μL | ||
KCTD17BA-20-GORE | 20 (40 μL) | 200 μL | ||
KCTD17BA-20-GRGO | 20 (40 μL) | 200 μL | ||
KCTD17BA-20-GROR | 20 (40 μL) | 200 μL | ||
KCTD17BA-20-GRRE | 20 (40 μL) | 200 μL | ||
KCTD17BA-20-REGO | 20 (40 μL) | 200 μL | ||
KCTD17BA-20-REGR | 20 (40 μL) | 200 μL |
Gene Summary
This gene encodes a protein that belongs to a conserved family of potassium channel tetramerization domain (KCTD)-containing proteins. The encoded protein functions in ciliogenesis by acting as a substrate adaptor for the cullin3-based ubiquitin-conjugating enzyme E3 ligase, and targets trichoplein, a keratin-binding protein, for degradation via polyubiquitinylation. A mutation in this gene is associated with autosomal dominant myoclonic dystonia 26. [provided by RefSeq, Nov 2016]
Gene Details
Gene Symbol: KCTD17
Gene Name: Potassium Channel Tetramerization Domain Containing 17
Chromosome: CHR22: 37447778-37459430
Locus: 22q12.3
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: KCTD17 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: KCTD17-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping