Gene-specific Copy Number Variation Probe-FLT1
Add to Cart
| Catalog: |
CNVFP-FLT1-05417 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FLT1). 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: |
FLT1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FLT1 genes. This product achieves the purpose of detection by hybridizing with the FLT1 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 |
Fms Related Tyrosine Kinase 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the vascular endothelial growth factor receptor (VEGFR) family. VEGFR family members are receptor tyrosine kinases (RTKs) which contain an extracellular ligand-binding region with seven immunoglobulin (Ig)-like domains, a transmembrane segment, and a tyrosine kinase (TK) domain within the cytoplasmic domain. This protein binds to VEGFR-A, VEGFR-B and placental growth factor and plays an important role in angiogenesis and vasculogenesis. Expression of this receptor is found in vascular endothelial cells, placental trophoblast cells and peripheral blood monocytes. Multiple transcript variants encoding different isoforms have been found for this gene. Isoforms include a full-length transmembrane receptor isoform and shortened, soluble isoforms. The soluble isoforms are associated with the onset of pre-eclampsia.[provided by RefSeq, May 2009] |
| Gene Symbol |
FLT1 |
| Location |
13q12.3 |
| Chromosome |
Chromosome13 |
| Coordinates |
This gene maps to 28874482-29069265 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-FLT1-05417-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FLT1-05417-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FLT1-05417-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FLT1-05417-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FLT1-05417-AQ |
467nm |
418nm |
|
Other Products
