Gene-specific Copy Number Variation Probe-BBS10
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| Catalog: |
CNVFP-BBS10-01452 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (BBS10). 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: |
BBS10 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to BBS10 genes. This product achieves the purpose of detection by hybridizing with the BBS10 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 |
Bardet-Biedl Syndrome 10 |
| Gene Summary [Provided by RefSeq] |
This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by progressive retinal degeneration, obesity, polydactyly, renal malformation and cognitive disability. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene is likely not a ciliary protein but rather has distant sequence homology to type II chaperonins. As a molecular chaperone, this protein may affect the folding or stability of other ciliary or basal body proteins. Inhibition of this protein's expression impairs ciliogenesis in preadipocytes. Mutations in this gene cause Bardet-Biedl syndrome type 10. [provided by RefSeq, Jan 2010] |
| Gene Symbol |
BBS10 |
| Location |
12q21.2 |
| Chromosome |
Chromosome12 |
| Coordinates |
This gene maps to 76738265-76742222 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-BBS10-01452-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-BBS10-01452-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-BBS10-01452-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-BBS10-01452-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-BBS10-01452-AQ |
467nm |
418nm |
|
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