Gene-specific Copy Number Variation Probe-SEMA4A
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| Catalog: |
CNVFP-SEMA4A-18285 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SEMA4A). 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: |
SEMA4A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SEMA4A genes. This product achieves the purpose of detection by hybridizing with the SEMA4A 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 |
Semaphorin 4A |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the semaphorin family of soluble and transmembrane proteins. Semaphorins are involved in numerous functions, including axon guidance, morphogenesis, carcinogenesis, and immunomodulation. The encoded protein is a single-pass type I membrane protein containing an immunoglobulin-like C2-type domain, a PSI domain and a sema domain. It inhibits axonal extension by providing local signals to specify territories inaccessible for growing axons. It is an activator of T-cell-mediated immunity and suppresses vascular endothelial growth factor (VEGF)-mediated endothelial cell migration and proliferation in vitro and angiogenesis in vivo. Mutations in this gene are associated with retinal degenerative diseases including retinitis pigmentosa type 35 (RP35) and cone-rod dystrophy type 10 (CORD10). Multiple alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Sep 2010] |
| Gene Symbol |
SEMA4A |
| Location |
1q22 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 156119734-156147542 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-SEMA4A-18285-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SEMA4A-18285-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SEMA4A-18285-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SEMA4A-18285-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SEMA4A-18285-AQ |
467nm |
418nm |
|
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