LRRC8A-CCBL1 Fusion FISH Probe
The LRRC8A-CCBL1 Fusion FISH Probe is used to confirm a fusion of the LRRC8A and CCBL1 genes. The fusion of the LRRC8A and CCBL1 genes has been associated with Breast Invasive 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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| LRRC8A-CCBL1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-RERE | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-REOR | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-REGO | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-REGR | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-REAQ | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-ORRE | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-OROR | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-ORGO | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-ORAQ | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-GORE | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-GOOR | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-GOGO | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-GOGR | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-GOAQ | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-GRRE | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-GROR | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-GRGO | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-GRGR | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-GRAQ | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-AQRE | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-AQOR | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-AQGO | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-AQGR | 20 (40 μL) | 200 μL |
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| LRRC8A-CCBL1-20-AQAQ | 20 (40 μL) | 200 μL |
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LRRC8A Gene Summary
This gene encodes a protein belonging to the leucine-rich repeat family of proteins, which are involved in diverse biological processes, including cell adhesion, cellular trafficking, and hormone-receptor interactions. This family member is a putative four-pass transmembrane protein that plays a role in B cell development. Defects in this gene cause autosomal dominant non-Bruton type agammaglobulinemia, an immunodeficiency disease resulting from defects in B cell maturation. Multiple alternatively spliced transcript variants, which encode the same protein, have been identified for this gene. [provided by RefSeq, Jul 2008]
Gene Name: Leucine Rich Repeat Containing 8 VRAC Subunit A
Chromosome: CHR9: 131644390 -131680317
Locus: 9q34.11
Gene Diseases
The LRRC8A CCBL1 Fusion has been associated with the following diseases:
| Disease Name |
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| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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