Gene-specific Copy Number Variation Probe-SEMA3C
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Catalog: |
CNVFP-SEMA3C-18289 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SEMA3C). 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: |
SEMA3C Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SEMA3C genes. This product achieves the purpose of detection by hybridizing with the SEMA3C 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 3C |
Gene Summary [Provided by RefSeq] |
This gene encodes a secreted glycoprotein that belongs to the semaphorin class 3 family of neuronal guidance cues. The encoded protein contains an N-terminal sema domain, integrin and immunoglobulin-like domains, and a C-terminal basic domain. Homodimerization and proteolytic cleavage of the C-terminal propeptide are necessary for the function of the encoded protein. It binds a neuropilin co-receptor before forming a heterotrimeric complex with an associated plexin. An increase in the expression of this gene correlates with an increase in cancer cell invasion and adhesion. Naturally occurring mutations in this gene are associated with Hirschsprung disease. [provided by RefSeq, May 2017] |
Gene Symbol |
SEMA3C |
Location |
7q21.11 |
Chromosome |
Chromosome7 |
Coordinates |
This gene maps to 80371853-80548667 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-SEMA3C-18289-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SEMA3C-18289-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SEMA3C-18289-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SEMA3C-18289-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SEMA3C-18289-AQ |
467nm |
418nm |
|
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