Gene-specific Copy Number Variation Probe-FGG
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| Catalog: |
CNVFP-FGG-05409 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FGG). 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: |
FGG Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FGG genes. This product achieves the purpose of detection by hybridizing with the FGG 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 |
Fibrinogen Gamma Chain |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is the gamma component of fibrinogen, a blood-borne glycoprotein comprised of three pairs of nonidentical polypeptide chains. Following vascular injury, fibrinogen is cleaved by thrombin to form fibrin which is the most abundant component of blood clots. In addition, various cleavage products of fibrinogen and fibrin regulate cell adhesion and spreading, display vasoconstrictor and chemotactic activities, and are mitogens for several cell types. Mutations in this gene lead to several disorders, including dysfibrinogenemia, hypofibrinogenemia and thrombophilia. Alternative splicing results in transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015] |
| Gene Symbol |
FGG |
| Location |
4q32.1 |
| Chromosome |
Chromosome4 |
| Coordinates |
This gene maps to 155525285-155533902 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-FGG-05409-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FGG-05409-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FGG-05409-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FGG-05409-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FGG-05409-AQ |
467nm |
418nm |
|
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