Gene-specific Copy Number Variation Probe-SPTBN2
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Catalog: |
CNVFP-SPTBN2-19959 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SPTBN2). 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: |
SPTBN2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SPTBN2 genes. This product achieves the purpose of detection by hybridizing with the SPTBN2 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 |
Spectrin Beta, Non-erythrocytic 2 |
Gene Summary [Provided by RefSeq] |
Spectrins are principle components of a cell's membrane-cytoskeleton and are composed of two alpha and two beta spectrin subunits. The protein encoded by this gene (SPTBN2), is called spectrin beta non-erythrocytic 2 or beta-III spectrin. It is related to, but distinct from, the beta-II spectrin gene which is also known as spectrin beta non-erythrocytic 1 (SPTBN1). SPTBN2 regulates the glutamate signaling pathway by stabilizing the glutamate transporter EAAT4 at the surface of the plasma membrane. Mutations in this gene cause a form of spinocerebellar ataxia, SCA5, that is characterized by neurodegeneration, progressive locomotor incoordination, dysarthria, and uncoordinated eye movements. [provided by RefSeq, Dec 2009] |
Gene Symbol |
SPTBN2 |
Location |
11q13.2 |
Chromosome |
Chromosome11 |
Coordinates |
This gene maps to 66452719-66488870 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-SPTBN2-19959-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SPTBN2-19959-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SPTBN2-19959-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SPTBN2-19959-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SPTBN2-19959-AQ |
467nm |
418nm |
|
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