Gene-specific Copy Number Variation Probe-COL9A1
Add to Cart
| Catalog: |
CNVFP-COL9A1-03165 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (COL9A1). 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: |
COL9A1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to COL9A1 genes. This product achieves the purpose of detection by hybridizing with the COL9A1 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 IX Alpha 1 Chain |
| Gene Summary [Provided by RefSeq] |
This gene encodes one of the three alpha chains of type IX collagen, which is a minor (5-20%) collagen component of hyaline cartilage. Type IX collagen is usually found in tissues containing type II collagen, a fibrillar collagen. Studies in knockout mice have shown that synthesis of the alpha 1 chain is essential for assembly of type IX collagen molecules, a heterotrimeric molecule, and that lack of type IX collagen is associated with early onset osteoarthritis. Mutations in this gene are associated with osteoarthritis in humans, with multiple epiphyseal dysplasia, 6, a form of chondrodysplasia, and with Stickler syndrome, a disease characterized by ophthalmic, orofacial, articular, and auditory defects. Two transcript variants that encode different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
COL9A1 |
| Location |
6q13 |
| Chromosome |
Chromosome6 |
| Coordinates |
This gene maps to 70925742-71012786 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-COL9A1-03165-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-COL9A1-03165-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-COL9A1-03165-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-COL9A1-03165-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-COL9A1-03165-AQ |
467nm |
418nm |
|
Other Products
