LCP2-SLC34A1 Fusion FISH Probe
The LCP2-SLC34A1 Fusion FISH Probe is used to confirm a fusion of the LCP2 and SLC34A1 genes. The fusion of the LCP2 and SLC34A1 genes has been associated with Skin Cutaneous Melanoma. 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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| LCP2-SLC34A1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-RERE | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-REOR | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-REGO | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-REGR | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-REAQ | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-ORRE | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-OROR | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-ORGO | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-ORAQ | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-GORE | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-GOOR | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-GOGO | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-GOGR | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-GOAQ | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-GRRE | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-GROR | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-GRGO | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-GRGR | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-GRAQ | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-AQRE | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-AQOR | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-AQGO | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-AQGR | 20 (40 μL) | 200 μL |
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| LCP2-SLC34A1-20-AQAQ | 20 (40 μL) | 200 μL |
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LCP2 Gene Summary
This gene encodes an adapter protein that acts as a substrate of the T cell antigen receptor (TCR)-activated protein tyrosine kinase pathway. The encoded protein associates with growth factor receptor bound protein 2, and is thought to play a role TCR-mediated intracellular signal transduction. A similar protein in mouse plays a role in normal T-cell development and activation. Mice lacking this gene show subcutaneous and intraperitoneal fetal hemorrhaging, dysfunctional platelets and impaired viability. [provided by RefSeq, Nov 2016]
Gene Name: Lymphocyte Cytosolic Protein 2
Chromosome: CHR5: 169675087 -169724822
Locus: 5q35.1
SLC34A1 Gene Summary
This gene encodes a member of the type II sodium-phosphate cotransporter family. Mutations in this gene are associated with hypophosphatemia nephrolithiasis/osteoporosis 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2009]
Gene Name: Solute Carrier Family 34 Member 1
Chromosome: CHR5: 176811431 -176825849
Locus: 5q35.3
Gene Diseases
The LCP2 SLC34A1 Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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