Gene-specific Copy Number Variation Probe-FGFR1OP
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| Catalog: |
CNVFP-FGFR1OP-05414 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FGFR1OP). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
| Application: |
FGFR1OP Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FGFR1OP genes. This product achieves the purpose of detection by hybridizing with the FGFR1OP gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
| Category: |
Copy Number Variation |
| Probe Kits Volume (µL): |
40 μL |
| Quantity: |
20 Tests |
| Hybridization Solution (µL): |
200 μL |
| Turnaround Time: |
7-10 Business Days |
| Shipping Time: |
1-2 Day Expedited Shipping |
| Storage Conditions: |
Store at -20℃ and avoid light; |
| Shipping Conditions: |
-20℃ |
Gene Details
| Gene Name |
FGFR1 Oncogene Partner |
| Gene Summary [Provided by RefSeq] |
This gene encodes a largely hydrophilic centrosomal protein that is required for anchoring microtubules to subcellular structures. A t(6;8)(q27;p11) chromosomal translocation, fusing this gene and the fibroblast growth factor receptor 1 (FGFR1) gene, has been found in cases of myeloproliferative disorder. The resulting chimeric protein contains the N-terminal leucine-rich region of this encoded protein fused to the catalytic domain of FGFR1. Alterations in this gene may also be associated with Crohn's disease, Graves' disease, and vitiligo. Alternatively spliced transcript variants that encode different proteins have been identified. [provided by RefSeq, Jul 2013] |
| Gene Symbol |
FGFR1OP |
| Location |
6q27 |
| Chromosome |
Chromosome6 |
| Coordinates |
This gene maps to 167412815-167454066 in GRCh37 coordinates. |
| Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
| Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
| 1 |
OR
|
CNVFP-FGFR1OP-05414-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FGFR1OP-05414-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FGFR1OP-05414-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FGFR1OP-05414-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FGFR1OP-05414-AQ |
467nm |
418nm |
|
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