Gene-specific Copy Number Variation Probe-RTTN
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| Catalog: |
CNVFP-RTTN-17680 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RTTN). 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: |
RTTN Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RTTN genes. This product achieves the purpose of detection by hybridizing with the RTTN 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 |
Rotatin |
| Gene Summary [Provided by RefSeq] |
This gene encodes a large protein whose specific function is unknown. Absence of the orthologous protein in mouse results in embryonic lethality with deficient axial rotation, abnormal differentiation of the neural tube, and randomized looping of the heart tube during development. In human, mutations in this gene are associated with polymicrogyria with seizures. In human fibroblasts this protein localizes at the ciliary basal bodies. Given the intracellular localization of this protein and the phenotypic effects of mutations, this gene is suspected of playing a role in the maintenance of normal ciliary structure which in turn effects the developmental process of left-right organ specification, axial rotation, and perhaps notochord development. [provided by RefSeq, Jan 2013] |
| Gene Symbol |
RTTN |
| Location |
18q22.2 |
| Chromosome |
Chromosome18 |
| Coordinates |
This gene maps to 67671042-67872962 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-RTTN-17680-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RTTN-17680-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RTTN-17680-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RTTN-17680-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RTTN-17680-AQ |
467nm |
418nm |
|
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