Gene-specific Copy Number Variation Probe-FTH1
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Catalog: |
CNVFP-FTH1-05522 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FTH1). 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: |
FTH1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FTH1 genes. This product achieves the purpose of detection by hybridizing with the FTH1 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 Heavy Chain 1 |
Gene Summary [Provided by RefSeq] |
This gene encodes the heavy subunit of ferritin, 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 ferritin proteins are associated with several neurodegenerative diseases. This gene has multiple pseudogenes. Several alternatively spliced transcript variants have been observed, but their biological validity has not been determined. [provided by RefSeq, Jul 2008] |
Gene Symbol |
FTH1 |
Location |
11q12.3 |
Chromosome |
Chromosome11 |
Coordinates |
This gene maps to 61731756-61735132 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-FTH1-05522-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-FTH1-05522-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-FTH1-05522-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-FTH1-05522-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-FTH1-05522-AQ |
467nm |
418nm |
|
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