Gene-specific Copy Number Variation Probe-INSR
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Catalog: |
CNVFP-INSR-07742 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (INSR). 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: |
INSR Gene-specific copy number variation probes are mainly used to detect the copy number variation related to INSR genes. This product achieves the purpose of detection by hybridizing with the INSR 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 |
Insulin Receptor |
Gene Summary [Provided by RefSeq] |
This gene encodes a member of the receptor tyrosine kinase family of proteins. The encoded preproprotein is proteolytically processed to generate alpha and beta subunits that form a heterotetrameric receptor. Binding of insulin or other ligands to this receptor activates the insulin signaling pathway, which regulates glucose uptake and release, as well as the synthesis and storage of carbohydrates, lipids and protein. Mutations in this gene underlie the inherited severe insulin resistance syndromes including type A insulin resistance syndrome, Donohue syndrome and Rabson-Mendenhall syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015] |
Gene Symbol |
INSR |
Location |
19p13.2 |
Chromosome |
Chromosome19 |
Coordinates |
This gene maps to 7112265-7294011 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-INSR-07742-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-INSR-07742-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-INSR-07742-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-INSR-07742-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-INSR-07742-AQ |
467nm |
418nm |
|
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