Gene-specific Copy Number Variation Probe-SMARCA4
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| Catalog: |
CNVFP-SMARCA4-19007 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SMARCA4). 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: |
SMARCA4 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SMARCA4 genes. This product achieves the purpose of detection by hybridizing with the SMARCA4 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 |
SWI/SNF Related, Matrix Associated, Actin Dependent Regulator Of Chromatin, Subfamily A, Member 4 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the SWI/SNF family of proteins and is similar to the brahma protein of Drosophila. Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI, which is required for transcriptional activation of genes normally repressed by chromatin. In addition, this protein can bind BRCA1, as well as regulate the expression of the tumorigenic protein CD44. Mutations in this gene cause rhabdoid tumor predisposition syndrome type 2. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012] |
| Gene Symbol |
SMARCA4 |
| Location |
19p13.2 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 11071597-11172958 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-SMARCA4-19007-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SMARCA4-19007-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SMARCA4-19007-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SMARCA4-19007-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SMARCA4-19007-AQ |
467nm |
418nm |
|
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