Gene-specific Copy Number Variation Probe-S100B
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| Catalog: |
CNVFP-S100B-17975 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (S100B). 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: |
S100B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to S100B genes. This product achieves the purpose of detection by hybridizing with the S100B 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 |
S100 Calcium Binding Protein B |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21; however, this gene is located at 21q22.3. This protein may function in Neurite extension, proliferation of melanoma cells, stimulation of Ca2+ fluxes, inhibition of PKC-mediated phosphorylation, astrocytosis and axonal proliferation, and inhibition of microtubule assembly. Chromosomal rearrangements and altered expression of this gene have been implicated in several neurological, neoplastic, and other types of diseases, including Alzheimer's disease, Down's syndrome, epilepsy, amyotrophic lateral sclerosis, melanoma, and type I diabetes. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
S100B |
| Location |
21q22.3 |
| Chromosome |
Chromosome21 |
| Coordinates |
This gene maps to 48018530-48025035 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-S100B-17975-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-S100B-17975-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-S100B-17975-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-S100B-17975-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-S100B-17975-AQ |
467nm |
418nm |
|
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