Gene-specific Copy Number Variation Probe-F9
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| Catalog: |
CNVFP-F9-04923 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (F9). 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: |
F9 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to F9 genes. This product achieves the purpose of detection by hybridizing with the F9 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 |
Coagulation Factor IX |
| Gene Summary [Provided by RefSeq] |
This gene encodes vitamin K-dependent coagulation factor IX that circulates in the blood as an inactive zymogen. This factor is converted to an active form by factor XIa, which excises the activation peptide and thus generates a heavy chain and a light chain held together by one or more disulfide bonds. The role of this activated factor IX in the blood coagulation cascade is to activate factor X to its active form through interactions with Ca+2 ions, membrane phospholipids, and factor VIII. Alterations of this gene, including point mutations, insertions and deletions, cause factor IX deficiency, which is a recessive X-linked disorder, also called hemophilia B or Christmas disease. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Sep 2015] |
| Gene Symbol |
F9 |
| Location |
Xq27.1 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 138612894-138645617 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-F9-04923-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-F9-04923-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-F9-04923-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-F9-04923-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-F9-04923-AQ |
467nm |
418nm |
|
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