Gene-specific Copy Number Variation Probe-SOHLH2
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| Catalog: |
CNVFP-SOHLH2-19791 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SOHLH2). 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: |
SOHLH2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SOHLH2 genes. This product achieves the purpose of detection by hybridizing with the SOHLH2 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 |
Spermatogenesis And Oogenesis Specific Basic Helix-loop-helix 2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes one of testis-specific transcription factors which are essential for spermatogenesis, oogenesis and folliculogenesis. This gene is located on chromosome 13. The proteins encoded by this gene and another testis-specific transcription factor, SOHLH1, can form heterodimers, in addition to homodimers. There is a read-through locus (GeneID: 100526761) that shares sequence identity with this gene and the upstream CCDC169 (GeneID: 728591). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013] |
| Gene Symbol |
SOHLH2 |
| Location |
13q13.3 |
| Chromosome |
Chromosome13 |
| Coordinates |
This gene maps to 36742344-36788752 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-SOHLH2-19791-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SOHLH2-19791-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SOHLH2-19791-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SOHLH2-19791-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SOHLH2-19791-AQ |
467nm |
418nm |
|
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