Gene-specific Copy Number Variation Probe-IFITM5
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| Catalog: |
CNVFP-IFITM5-07114 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (IFITM5). 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: |
IFITM5 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to IFITM5 genes. This product achieves the purpose of detection by hybridizing with the IFITM5 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 |
Interferon Induced Transmembrane Protein 5 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a membrane protein thought to play a role in bone mineralization. This gene is located on chromosome 11 in a cluster of related genes which are induced by interferon, however, this gene has not been shown to be interferon inducible. A similar gene, located in a gene cluster on mouse chromosome 7, is a member of the interferon-inducible fragilis gene family. The mouse gene encodes a transmembrane protein described as participating in germ cell competence. A mutation in the 5' UTR of this gene has been associated with osteogenesis imperfecta type V (PMID: 22863190, 22863195). [provided by RefSeq, Aug 2012] |
| Gene Symbol |
IFITM5 |
| Location |
11p15.5 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 298202-299526 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-IFITM5-07114-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-IFITM5-07114-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-IFITM5-07114-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-IFITM5-07114-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-IFITM5-07114-AQ |
467nm |
418nm |
|
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