KCTD1 Break Apart FISH Probe
Empire Genomics’ KCTD1 Break Apart FISH Probe is designed to flank the KCTD1 gene and is typically used for detecting KCTD1 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 |
---|---|---|---|---|
KCTD1BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL | ||
KCTD1BA-20-AQOR | 20 (40 μL) | 200 μL | ||
KCTD1BA-20-GOGR | 20 (40 μL) | 200 μL | ||
KCTD1BA-20-GORE | 20 (40 μL) | 200 μL | ||
KCTD1BA-20-GRGO | 20 (40 μL) | 200 μL | ||
KCTD1BA-20-GRRE | 20 (40 μL) | 200 μL | ||
KCTD1BA-20-ORGR | 20 (40 μL) | 200 μL | ||
KCTD1BA-20-REGO | 20 (40 μL) | 200 μL | ||
KCTD1BA-20-REGR | 20 (40 μL) | 200 μL |
Gene Summary
This gene encodes a protein containing a BTB (Broad-complex, tramtrack and bric a brac), also known as a POZ (POxvirus and zinc finger) protein-protein interaction domain. The encoded protein negatively regulates the AP-2 family of transcription factors and the Wnt signaling pathway. A mechanism for the modulation of Wnt signaling has been proposed in which the encoded protein enhances ubiquitination and degradation of the beta-catenin protein. Mutations in this gene have been identified in Scalp-ear-nipple (SEN) syndrome. [provided by RefSeq, May 2017]
Gene Details
Gene Symbol: KCTD1
Gene Name: Potassium Channel Tetramerization Domain Containing 1
Chromosome: CHR18: 24034874-24220308
Locus: 18q11.2
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: KCTD1 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: KCTD1-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping