Gene-specific Copy Number Variation Probe-COL4A6
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| Catalog: |
CNVFP-COL4A6-03175 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (COL4A6). 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: |
COL4A6 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to COL4A6 genes. This product achieves the purpose of detection by hybridizing with the COL4A6 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 |
Collagen Type IV Alpha 6 Chain |
| Gene Summary [Provided by RefSeq] |
This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene, alpha 5 type IV collagen, so that the gene pair shares a common promoter. Deletions in the alpha 5 gene that extend into the alpha 6 gene result in diffuse leiomyomatosis accompanying the X-linked Alport syndrome caused by the deletion in the alpha 5 gene. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2013] |
| Gene Symbol |
COL4A6 |
| Location |
Xq22.3 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 107398836-107682704 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-COL4A6-03175-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-COL4A6-03175-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-COL4A6-03175-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-COL4A6-03175-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-COL4A6-03175-AQ |
467nm |
418nm |
|
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