Gene-specific Copy Number Variation Probe-HCST
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| Catalog: |
CNVFP-HCST-06660 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HCST). 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: |
HCST Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HCST genes. This product achieves the purpose of detection by hybridizing with the HCST 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 |
Hematopoietic Cell Signal Transducer |
| Gene Summary [Provided by RefSeq] |
This gene encodes a transmembrane signaling adaptor that contains a YxxM motif in its cytoplasmic domain. The encoded protein may form part of the immune recognition receptor complex with the C-type lectin-like receptor NKG2D. As part of this receptor complex, this protein may activate phosphatidylinositol 3-kinase dependent signaling pathways through its intracytoplasmic YxxM motif. This receptor complex may have a role in cell survival and proliferation by activation of NK and T cell responses. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
HCST |
| Location |
19q13.12 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 36393381-36395173 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-HCST-06660-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HCST-06660-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HCST-06660-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HCST-06660-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HCST-06660-AQ |
467nm |
418nm |
|
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