SQSTM1-IQCE Fusion FISH Probe
The SQSTM1-IQCE Fusion FISH Probe is used to confirm a fusion of the SQSTM1 and IQCE genes. The fusion of the SQSTM1 and IQCE genes has been associated with Adrenocortical Carcinoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.
** 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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SQSTM1-IQCE-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-RERE | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-REOR | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-REGO | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-REGR | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-REAQ | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-ORRE | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-OROR | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-ORGO | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-ORAQ | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-GORE | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-GOOR | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-GOGO | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-GOGR | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-GOAQ | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-GRRE | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-GROR | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-GRGO | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-GRGR | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-GRAQ | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-AQRE | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-AQOR | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-AQGO | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-AQGR | 20 (40 μL) | 200 μL | ||
SQSTM1-IQCE-20-AQAQ | 20 (40 μL) | 200 μL |
SQSTM1 Gene Summary
This gene encodes a multifunctional protein that binds ubiquitin and regulates activation of the nuclear factor kappa-B (NF-kB) signaling pathway. The protein functions as a scaffolding/adaptor protein in concert with TNF receptor-associated factor 6 to mediate activation of NF-kB in response to upstream signals. Alternatively spliced transcript variants encoding either the same or different isoforms have been identified for this gene. Mutations in this gene result in sporadic and familial Paget disease of bone. [provided by RefSeq, Mar 2009]
Gene Name: Sequestosome 1
Chromosome: CHR5: 179233387 -179265077
Locus: 5q35.3
IQCE Gene Summary
The IQ Motif Containing E (IQCE) gene is located on chr7 :2598631-2654368 at 7p22.3.
Gene Name: IQ Motif Containing E
Chromosome: CHR7: 2598631 -2654368
Locus: 7p22.3
Gene Diseases
The SQSTM1 IQCE Fusion has been associated with the following diseases:
Disease Name |
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Adrenocortical Carcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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