KLHL24-ATP11B Fusion FISH Probe
The KLHL24-ATP11B Fusion FISH Probe is used to confirm a fusion of the KLHL24 and ATP11B genes. The fusion of the KLHL24 and ATP11B genes has been associated with Kidney Renal Papillary Cell 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
SKU | Test Kits | Buffer | Dye Color | Order Now |
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KLHL24-ATP11B-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-RERE | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-REOR | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-REGO | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-REGR | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-REAQ | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-ORRE | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-OROR | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-ORGO | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-ORAQ | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-GORE | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-GOOR | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-GOGO | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-GOGR | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-GOAQ | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-GRRE | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-GROR | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-GRGO | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-GRGR | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-GRAQ | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-AQRE | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-AQOR | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-AQGO | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-AQGR | 20 (40 μL) | 200 μL |
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KLHL24-ATP11B-20-AQAQ | 20 (40 μL) | 200 μL |
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ATP11B Gene Summary
P-type ATPases, such as ATP11B, are phosphorylated in their intermediate state and drive uphill transport of ions across membranes. Several subfamilies of P-type ATPases have been identified. One subfamily transports heavy metal ions, such as Cu(2+) or Cd(2+). Another subfamily transports non-heavy metal ions, such as H(+), Na(+), K(+), or Ca(+). A third subfamily transports amphipaths, such as phosphatidylserine.[supplied by OMIM, Feb 2005]
Gene Name: ATPase Phospholipid Transporting 11B (putative)
Chromosome: CHR3: 182511290 -182639421
Locus: 3q26.33
KLHL24 Gene Summary
The protein encoded by this gene is a ubiquitin ligase substrate receptor and is regulated by autoubiquitination. Variations in the translation initiation codon of this gene have been found, which result in an N-terminally truncated but more stable protein due to loss of the autoubiquitination function. The more stable mutant protein causes an increased ubiquitin and degradation of keratin 14, which leads to skin fragility and the potentially life-threatening disease epidermolysis bullosa. The encoded protein is also involved in the regulation of kainate receptors. [provided by RefSeq, Mar 2017]
Gene Name: Kelch Like Family Member 24
Chromosome: CHR3: 183353410 -183402304
Locus: 3q27.1
Gene Diseases
The KLHL24 ATP11B Fusion has been associated with the following diseases:
Disease Name |
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Kidney Renal Papillary Cell Carcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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