ERBB2-SLC29A3 Fusion FISH Probe
The ERBB2-SLC29A3 Fusion FISH Probe is used to confirm a fusion of the ERBB2 and SLC29A3 genes. The fusion of the ERBB2 and SLC29A3 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| ERBB2-SLC29A3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-RERE | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-REOR | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-REGO | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-REGR | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-REAQ | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-ORRE | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-OROR | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-ORGO | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-ORAQ | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-GORE | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-GOOR | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-GOGO | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-GOGR | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-GOAQ | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-GRRE | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-GROR | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-GRGO | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-GRGR | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-GRAQ | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-AQRE | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-AQOR | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-AQGO | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-AQGR | 20 (40 μL) | 200 μL |
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| ERBB2-SLC29A3-20-AQAQ | 20 (40 μL) | 200 μL |
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ERBB2 Gene Summary
This gene encodes a member of the epidermal growth factor (EGF) receptor family of receptor tyrosine kinases. This protein has no ligand binding domain of its own and therefore cannot bind growth factors. However, it does bind tightly to other ligand-bound EGF receptor family members to form a heterodimer, stabilizing ligand binding and enhancing kinase-mediated activation of downstream signalling pathways, such as those involving mitogen-activated protein kinase and phosphatidylinositol-3 kinase. Allelic variations at amino acid positions 654 and 655 of isoform a (positions 624 and 625 of isoform b) have been reported, with the most common allele, Ile654/Ile655, shown here. Amplification and/or overexpression of this gene has been reported in numerous cancers, including breast and ovarian tumors. Alternative splicing results in several additional transcript variants, some encoding different isoforms and others that have not been fully characterized. [provided by RefSeq, Jul 2008]
Gene Name: Erb-b2 Receptor Tyrosine Kinase 2
Chromosome: CHR17: 37844392 -37884915
Locus: 17q12
SLC29A3 Gene Summary
This gene encodes a nucleoside transporter. The encoded protein plays a role in cellular uptake of nucleosides, nucleobases, and their related analogs. Mutations in this gene have been associated with H syndrome, which is characterized by cutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism. A related disorder, PHID (pigmented hypertrichosis with insulin-dependent diabetes mellitus), has also been associated with mutations at this locus. Alternatively spliced transcript variants have been described.[provided by RefSeq, Mar 2010]
Gene Name: Solute Carrier Family 29 Member 3
Chromosome: CHR10: 73079009 -73123147
Locus: 10q22.1
Gene Diseases
The ERBB2 SLC29A3 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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