Gene-specific Copy Number Variation Probe-FTL
Add to Cart
| Catalog: |
CNVFP-FTL-05520 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FTL). 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: |
FTL Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FTL genes. This product achieves the purpose of detection by hybridizing with the FTL 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 |
Ferritin Light Chain |
| Gene Summary [Provided by RefSeq] |
This gene encodes the light subunit of the ferritin protein. Ferritin is the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits of the heavy and light ferritin chains. Variation in ferritin subunit composition may affect the rates of iron uptake and release in different tissues. A major function of ferritin is the storage of iron in a soluble and nontoxic state. Defects in this light chain ferritin gene are associated with several neurodegenerative diseases and hyperferritinemia-cataract syndrome. This gene has multiple pseudogenes. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
FTL |
| Location |
19q13.33 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 49468565-49470136 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-FTL-05520-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FTL-05520-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FTL-05520-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FTL-05520-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FTL-05520-AQ |
467nm |
418nm |
|
Other Products
