Gene-specific Copy Number Variation Probe-HSPB1
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| Catalog: |
CNVFP-HSPB1-06897 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HSPB1). 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: |
HSPB1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HSPB1 genes. This product achieves the purpose of detection by hybridizing with the HSPB1 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 |
Heat Shock Protein Family B (small) Member 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the small heat shock protein (HSP20) family of proteins. In response to environmental stress, the encoded protein translocates from the cytoplasm to the nucleus and functions as a molecular chaperone that promotes the correct folding of other proteins. This protein plays an important role in the differentiation of a wide variety of cell types. Expression of this gene is correlated with poor clinical outcome in multiple human cancers, and the encoded protein may promote cancer cell proliferation and metastasis, while protecting cancer cells from apoptosis. Mutations in this gene have been identified in human patients with Charcot-Marie-Tooth disease and distal hereditary motor neuropathy. [provided by RefSeq, Aug 2017] |
| Gene Symbol |
HSPB1 |
| Location |
7q11.23 |
| Chromosome |
Chromosome7 |
| Coordinates |
This gene maps to 75931874-75933614 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-HSPB1-06897-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HSPB1-06897-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HSPB1-06897-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HSPB1-06897-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HSPB1-06897-AQ |
467nm |
418nm |
|
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