Gene-specific Copy Number Variation Probe-SMC1A
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| Catalog: |
CNVFP-SMC1A-18996 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SMC1A). 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: |
SMC1A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SMC1A genes. This product achieves the purpose of detection by hybridizing with the SMC1A 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 |
Structural Maintenance Of Chromosomes 1A |
| Gene Summary [Provided by RefSeq] |
Proper cohesion of sister chromatids is a prerequisite for the correct segregation of chromosomes during cell division. The cohesin multiprotein complex is required for sister chromatid cohesion. This complex is composed partly of two structural maintenance of chromosomes (SMC) proteins, SMC3 and either SMC1B or the protein encoded by this gene. Most of the cohesin complexes dissociate from the chromosomes before mitosis, although those complexes at the kinetochore remain. Therefore, the encoded protein is thought to be an important part of functional kinetochores. In addition, this protein interacts with BRCA1 and is phosphorylated by ATM, indicating a potential role for this protein in DNA repair. This gene, which belongs to the SMC gene family, is located in an area of the X-chromosome that escapes X inactivation. Mutations in this gene result in Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013] |
| Gene Symbol |
SMC1A |
| Location |
Xp11.22 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 53401069-53449618 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-SMC1A-18996-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SMC1A-18996-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SMC1A-18996-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SMC1A-18996-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SMC1A-18996-AQ |
467nm |
418nm |
|
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