Gene-specific Copy Number Variation Probe-IFT122
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Catalog: |
CNVFP-IFT122-07093 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (IFT122). 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: |
IFT122 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to IFT122 genes. This product achieves the purpose of detection by hybridizing with the IFT122 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 |
Intraflagellar Transport 122 |
Gene Summary [Provided by RefSeq] |
This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This cytoplasmic protein contains seven WD repeats and an AF-2 domain which function by recruiting coregulatory molecules and in transcriptional activation. Mutations in this gene cause cranioectodermal dysplasia-1. A related pseudogene is located on chromosome 3. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013] |
Gene Symbol |
IFT122 |
Location |
3q21.3-q22.1 |
Chromosome |
Chromosome3 |
Coordinates |
This gene maps to 129158967-129239191 in GRCh37 coordinates. |
Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
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1 |
OR
|
CNVFP-IFT122-07093-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-IFT122-07093-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-IFT122-07093-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-IFT122-07093-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-IFT122-07093-AQ |
467nm |
418nm |
|
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