Gene-specific Copy Number Variation Probe-HBS1L
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| Catalog: |
CNVFP-HBS1L-06692 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HBS1L). 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: |
HBS1L Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HBS1L genes. This product achieves the purpose of detection by hybridizing with the HBS1L 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 |
HBS1 Like Translational GTPase |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the GTP-binding elongation factor family. It is expressed in multiple tissues with the highest expression in heart and skeletal muscle. The intergenic region of this gene and the MYB gene has been identified to be a quantitative trait locus (QTL) controlling fetal hemoglobin level, and this region influnces erythrocyte, platelet, and monocyte counts as well as erythrocyte volume and hemoglobin content. DNA polymorphisms at this region associate with fetal hemoglobin levels and pain crises in sickle cell disease. A single nucleotide polymorphism in exon 1 of this gene is significantly associated with severity in beta-thalassemia/Hemoglobin E. Multiple alternatively spliced transcript variants encoding different protein isoforms have been found for this gene. [provided by RefSeq, May 2009] |
| Gene Symbol |
HBS1L |
| Location |
6q23.3 |
| Chromosome |
Chromosome6 |
| Coordinates |
This gene maps to 135281516-135376036 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-HBS1L-06692-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HBS1L-06692-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HBS1L-06692-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HBS1L-06692-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HBS1L-06692-AQ |
467nm |
418nm |
|
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