Gene-specific Copy Number Variation Probe-COL11A2
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| Catalog: |
CNVFP-COL11A2-02891 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (COL11A2). 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: |
COL11A2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to COL11A2 genes. This product achieves the purpose of detection by hybridizing with the COL11A2 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 XI Alpha 2 Chain |
| Gene Summary [Provided by RefSeq] |
This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. It is located on chromosome 6 very close to but separate from the gene for retinoid X receptor beta. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Proteolytic processing of this type XI chain produces PARP, a proline/arginine-rich protein that is an amino terminal domain. Mutations in this gene are associated with type III Stickler syndrome, otospondylomegaepiphyseal dysplasia (OSMED syndrome), Weissenbacher-Zweymuller syndrome, autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13), and autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53). Alternative splicing results in multiple transcript variants. A related pseudogene is located nearby on chromosome 6. [provided by RefSeq, Jul 2009] |
| Gene Symbol |
COL11A2 |
| Location |
6p21.32 |
| Chromosome |
Chromosome6_dbb_hap3 |
| Coordinates |
This gene maps to 4411775-4441552 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-COL11A2-02891-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-COL11A2-02891-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-COL11A2-02891-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-COL11A2-02891-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-COL11A2-02891-AQ |
467nm |
418nm |
|
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