CBLL1-SLC26A4 Fusion FISH Probe
The CBLL1-SLC26A4 Fusion FISH Probe is used to confirm a fusion of the CBLL1 and SLC26A4 genes. The fusion of the CBLL1 and SLC26A4 genes has been associated with Lung Adenocarcinoma. 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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| CBLL1-SLC26A4-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-RERE | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-REOR | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-REGO | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-REGR | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-REAQ | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-ORRE | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-OROR | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-ORGO | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-ORAQ | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-GORE | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-GOOR | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-GOGO | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-GOGR | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-GOAQ | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-GRRE | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-GROR | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-GRGO | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-GRGR | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-GRAQ | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-AQRE | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-AQOR | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-AQGO | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-AQGR | 20 (40 μL) | 200 μL |
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| CBLL1-SLC26A4-20-AQAQ | 20 (40 μL) | 200 μL |
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SLC26A4 Gene Summary
Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters. [provided by RefSeq, Jul 2008]
Gene Name: Solute Carrier Family 26 Member 4
Chromosome: CHR7: 107301079 -107358252
Locus: 7q22.3
CBLL1 Gene Summary
This gene encodes an E3 ubiquitin-ligase for the E-cadherin complex and mediates its ubiquitination, endocytosis, and degradation in the lysosomes. The encoded protein contains a RING-finger domain and is also thought to have a role in control of cell proliferation. A related pseudogene has been identified on chromosome X. Alternative splicing results in a non-coding transcript variant. [provided by RefSeq, Aug 2011]
Gene Name: Cbl Proto-oncogene Like 1
Chromosome: CHR7: 107384278 -107402083
Locus: 7q22.3
Gene Diseases
The CBLL1 SLC26A4 Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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