Gene-specific Copy Number Variation Probe-SIM1
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| Catalog: |
CNVFP-SIM1-18329 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SIM1). 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: |
SIM1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SIM1 genes. This product achieves the purpose of detection by hybridizing with the SIM1 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 |
Single-minded Family BHLH Transcription Factor 1 |
| Gene Summary [Provided by RefSeq] |
SIM1 and SIM2 genes are Drosophila single-minded (sim) gene homologs. SIM1 transcript was detected only in fetal kidney out of various adult and fetal tissues tested. Since the sim gene plays an important role in Drosophila development and has peak levels of expression during the period of neurogenesis,it was proposed that the human SIM gene is a candidate for involvement in certain dysmorphic features (particularly the facial and skull characteristics), abnormalities of brain development, and/or cognitive disability of Down syndrome. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
SIM1 |
| Location |
6q16.3 |
| Chromosome |
Chromosome6 |
| Coordinates |
This gene maps to 100836749-100911551 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-SIM1-18329-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SIM1-18329-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SIM1-18329-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SIM1-18329-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SIM1-18329-AQ |
467nm |
418nm |
|
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