Gene-specific Copy Number Variation Probe-VPS33B
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| Catalog: |
CNVFP-VPS33B-22818 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (VPS33B). 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: |
VPS33B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to VPS33B genes. This product achieves the purpose of detection by hybridizing with the VPS33B 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 |
VPS33B, Late Endosome And Lysosome Associated |
| Gene Summary [Provided by RefSeq] |
Vesicle mediated protein sorting plays an important role in segregation of intracellular molecules into distinct organelles. Genetic studies in yeast have identified more than 40 vacuolar protein sorting (VPS) genes involved in vesicle transport to vacuoles. This gene is a member of the Sec-1 domain family, and encodes the human ortholog of rat Vps33b which is homologous to the yeast class C Vps33 protein. The mammalian class C vacuolar protein sorting proteins are predominantly associated with late endosomes/lysosomes, and like their yeast counterparts, may mediate vesicle trafficking steps in the endosome/lysosome pathway. Mutations in this gene are associated with arthrogryposis-renal dysfunction-cholestasis syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014] |
| Gene Symbol |
VPS33B |
| Location |
15q26.1 |
| Chromosome |
Chromosome15 |
| Coordinates |
This gene maps to 91541773-91565833 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-VPS33B-22818-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-VPS33B-22818-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-VPS33B-22818-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-VPS33B-22818-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-VPS33B-22818-AQ |
467nm |
418nm |
|
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