Gene-specific Copy Number Variation Probe-ROR2
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| Catalog: |
CNVFP-ROR2-17594 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ROR2). 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: |
ROR2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ROR2 genes. This product achieves the purpose of detection by hybridizing with the ROR2 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 |
Receptor Tyrosine Kinase Like Orphan Receptor 2 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
ROR2 |
| Location |
9q22.31 |
| Chromosome |
Chromosome9 |
| Coordinates |
This gene maps to 94484877-94712444 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-ROR2-17594-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ROR2-17594-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ROR2-17594-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ROR2-17594-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ROR2-17594-AQ |
467nm |
418nm |
|
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