Gene-specific Copy Number Variation Probe-ADAM22
Add to Cart
| Catalog: |
CNVFP-ADAM22-00021 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ADAM22). 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: |
ADAM22 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ADAM22 genes. This product achieves the purpose of detection by hybridizing with the ADAM22 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 |
| 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 |
ADAM Metallopeptidase Domain 22 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. Unlike other members of the ADAM protein family, the protein encoded by this gene lacks metalloprotease activity since it has no zinc-binding motif. This gene is highly expressed in the brain and may function as an integrin ligand in the brain. In mice, it has been shown to be essential for correct myelination in the peripheral nervous system. Alternative splicing results in several transcript variants.[provided by RefSeq, Dec 2010] |
| Gene Symbol |
ADAM22 |
| Location |
7q21.12 |
| Chromosome |
Chromosome7 |
| Coordinates |
This gene maps to 87563565-87832204 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-ADAM22-00021-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ADAM22-00021-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ADAM22-00021-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ADAM22-00021-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ADAM22-00021-AQ |
467nm |
418nm |
|
Other Products
