Gene-specific Copy Number Variation Probe-SH3GL1
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Catalog: |
CNVFP-SH3GL1-18420 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SH3GL1). 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: |
SH3GL1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SH3GL1 genes. This product achieves the purpose of detection by hybridizing with the SH3GL1 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 |
SH3 Domain Containing GRB2 Like 1, Endophilin A2 |
Gene Summary [Provided by RefSeq] |
This gene encodes a member of the endophilin family of Src homology 3 domain-containing proteins. The encoded protein is involved in endocytosis and may also play a role in the cell cycle. Overexpression of this gene may play a role in leukemogenesis, and the encoded protein has been implicated in acute myeloid leukemia as a fusion partner of the myeloid-lymphoid leukemia protein. Pseudogenes of this gene are located on the long arm of chromosomes 11 and 17. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011] |
Gene Symbol |
SH3GL1 |
Location |
19p13.3 |
Chromosome |
Chromosome19 |
Coordinates |
This gene maps to 4360363-4400565 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-SH3GL1-18420-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SH3GL1-18420-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SH3GL1-18420-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SH3GL1-18420-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SH3GL1-18420-AQ |
467nm |
418nm |
|
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