Gene-specific Copy Number Variation Probe-MID1
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| Catalog: |
CNVFP-MID1-11147 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MID1). 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: |
MID1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MID1 genes. This product achieves the purpose of detection by hybridizing with the MID1 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 |
Midline 1 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the tripartite motif (TRIM) family, also known as the 'RING-B box-coiled coil' (RBCC) subgroup of RING finger proteins. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein forms homodimers which associate with microtubules in the cytoplasm. The protein is likely involved in the formation of multiprotein structures acting as anchor points to microtubules. Mutations in this gene have been associated with the X-linked form of Opitz syndrome, which is characterized by midline abnormalities such as cleft lip, laryngeal cleft, heart defects, hypospadias, and agenesis of the corpus callosum. This gene was also the first example of a gene subject to X inactivation in human while escaping it in mouse. Alternative promoter use, alternative splicing and alternative polyadenylation result in multiple transcript variants that have different tissue specificities. [provided by RefSeq, Dec 2016] |
| Gene Symbol |
MID1 |
| Location |
Xp22.2 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 10413349-10851809 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-MID1-11147-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-MID1-11147-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-MID1-11147-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-MID1-11147-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-MID1-11147-AQ |
467nm |
418nm |
|
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