Gene-specific Copy Number Variation Probe-RAB33B
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| Catalog: |
CNVFP-RAB33B-16877 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RAB33B). 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: |
RAB33B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RAB33B genes. This product achieves the purpose of detection by hybridizing with the RAB33B 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 |
RAB33B, Member RAS Oncogene Family |
| Gene Summary [Provided by RefSeq] |
This gene encodes a small GTP-binding protein of the Rab GTPase family, whose members function in vesicle transport during protein secretion and endocytosis. Rab GTPases are active, membrane-associated proteins that recruit effector proteins in the GTP-bound state and inactive cytosolic proteins when in a GDP-bound state. The protein encoded by this gene is ubiquitously expressed and has been implicated in Golgi to endoplasmic reticulum cycling of Golgi enzymes. In addition, this protein regulates Golgi homeostasis and coordinates intra-Golgi retrograde trafficking. Allelic variants in this gene have been associated with Dyggve-Melchior-Clausen syndrome and Smith-McCort dysplasia 2, which are autosomal recessive spondyloepimetaphyseal dysplasias characterized by skeletal abnormalities. [provided by RefSeq, Sep 2016] |
| Gene Symbol |
RAB33B |
| Location |
4q31.1 |
| Chromosome |
Chromosome4 |
| Coordinates |
This gene maps to 140374960-140397069 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-RAB33B-16877-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RAB33B-16877-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RAB33B-16877-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RAB33B-16877-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RAB33B-16877-AQ |
467nm |
418nm |
|
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