Gene-specific Copy Number Variation Probe-BMPR2
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Catalog: |
CNVFP-BMPR2-01599 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (BMPR2). 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: |
BMPR2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to BMPR2 genes. This product achieves the purpose of detection by hybridizing with the BMPR2 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 |
Bone Morphogenetic Protein Receptor Type 2 |
Gene Summary [Provided by RefSeq] |
This gene encodes a member of the bone morphogenetic protein (BMP) receptor family of transmembrane serine/threonine kinases. The ligands of this receptor are BMPs, which are members of the TGF-beta superfamily. BMPs are involved in endochondral bone formation and embryogenesis. These proteins transduce their signals through the formation of heteromeric complexes of two different types of serine (threonine) kinase receptors: type I receptors of about 50-55 kD and type II receptors of about 70-80 kD. Type II receptors bind ligands in the absence of type I receptors, but they require their respective type I receptors for signaling, whereas type I receptors require their respective type II receptors for ligand binding. Mutations in this gene have been associated with primary pulmonary hypertension, both familial and fenfluramine-associated, and with pulmonary venoocclusive disease. [provided by RefSeq, Jul 2008] |
Gene Symbol |
BMPR2 |
Location |
2q33.1-q33.2 |
Chromosome |
Chromosome2 |
Coordinates |
This gene maps to 203241049-203432474 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-BMPR2-01599-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-BMPR2-01599-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-BMPR2-01599-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-BMPR2-01599-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-BMPR2-01599-AQ |
467nm |
418nm |
|
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