Gene-specific Copy Number Variation Probe-SMARCAL1
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Catalog: |
CNVFP-SMARCAL1-19003 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SMARCAL1). 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: |
SMARCAL1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SMARCAL1 genes. This product achieves the purpose of detection by hybridizing with the SMARCAL1 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 Like 1 |
Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the SWI/SNF family of proteins. 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 shows sequence similarity to the E. coli RNA polymerase-binding protein HepA. Mutations in this gene are a cause of Schimke immunoosseous dysplasia (SIOD), an autosomal recessive disorder with the diagnostic features of spondyloepiphyseal dysplasia, renal dysfunction, and T-cell immunodeficiency. [provided by RefSeq, Jul 2008] |
Gene Symbol |
SMARCAL1 |
Location |
2q35 |
Chromosome |
Chromosome2 |
Coordinates |
This gene maps to 217277136-217347774 in GRCh37 coordinates. |
Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
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1 |
OR
|
CNVFP-SMARCAL1-19003-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SMARCAL1-19003-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SMARCAL1-19003-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SMARCAL1-19003-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SMARCAL1-19003-AQ |
467nm |
418nm |
|
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