SYNGAP1-COL11A2 Gene Fusion FISH Probe
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Catalog: |
GFFP-SYNGAP1/COL11A2-11604 |
Classification: |
Gene Fusion FISH Probes |
Description: |
The SYNGAP1-COL11A2 Gene Fusion FISH Probecan detect the fusion of SYNGAP1 and COL11A2 genes. Our product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We offer a variety of dye color combinations for FISH probes for gene fusions. This product has been verified in both interphase nuclei and metaphase spreads of normal peripheral blood. This is key quality control, you can trust our quality. |
Category: |
Gene Fusion FISH Probes |
Application: |
SYNGAP1-COL11A2 Gene Fusion FISH Probe can be used for chromosomal diagnosis to determine gene fusion phenomena associated with diseases such as cancer. You can confirm this in "Associated Diseases" in the product information. This product has been verified in both interphase nuclei and metaphase spreads of normal peripheral blood. This is key quality control, you can trust our quality. |
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 1 |
Collagen Type XI Alpha 2 Chain |
Gene Summary 1 |
This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. It is located on chromosome 6 very close to but separate from the gene for retinoid X receptor beta. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Proteolytic processing of this type XI chain produces PARP, a proline/arginine-rich protein that is an amino terminal domain. Mutations in this gene are associated with type III Stickler syndrome, otospondylomegaepiphyseal dysplasia (OSMED syndrome), Weissenbacher-Zweymuller syndrome, autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13), and autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53). Alternative splicing results in multiple transcript variants. A related pseudogene is located nearby on chromosome 6. [provided by RefSeq, Jul 2009] |
Chromosome 1 |
Chromosome 6_dbb_hap3 |
Locus 1 |
6p21.32 |
Coordinates 1 |
This gene maps to 4411775-4441552 in GRCh37 coordinates. |
Gene Name 2 |
Synaptic Ras GTPase Activating Protein 1 |
Gene Summary 2 |
This gene encodes a Ras GTPase activating protein that is a member of the N-methyl-D-aspartate receptor complex. The N-terminal domain of the protein contains a Ras-GAP domain, a pleckstrin homology domain, and a C2 domain that may be involved in binding of calcium and phospholipids. The C-terminal domain consists of a ten histidine repeat region, serine and tyrosine phosphorylation sites, and a T/SXV motif required for postsynaptic scaffold protein interaction. The encoded protein negatively regulates Ras, Rap and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor trafficking to the postsynaptic membrane to regulate synaptic plasticity and neuronal homeostasis. Allelic variants of this gene are associated with intellectual disability and autism spectrum disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016] |
Chromosome 2 |
Chromosome6 |
Locus 2 |
6p21.32 |
Coordinates 2 |
This gene maps to 33387846-33421466 in GRCh37 coordinates. |
Associated Diseases |
Pancreatic Adenocarcinoma |
Species |
Human |
Dye Colors:
RE
RE
RE
OR
RE
GO
RE
GR
RE
AQ
OR
RE
OR
OR
OR
GO
OR
GR
OR
AQ
GO
RE
GO
OR
GO
GO
GO
GR
GO
AQ
GR
RE
GR
OR
GR
GO
GR
GR
GR
AQ
AQ
RE
AQ
OR
AQ
GO
AQ
GR
AQ
AQ
Order Sheet
Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
1 |
RE; RE
|
GFFP-SYNGAP1/COL11A2-11604-RERE |
599nm;599nm |
580nm;580nm |
|
2 |
RE; OR
|
GFFP-SYNGAP1/COL11A2-11604-REOR |
599nm;573nm |
580nm;548nm |
|
3 |
RE; GO
|
GFFP-SYNGAP1/COL11A2-11604-REGO |
599nm;551nm |
580nm;525nm |
|
4 |
RE; GR
|
GFFP-SYNGAP1/COL11A2-11604-REGR |
599nm;515nm |
580nm;491nm |
|
5 |
RE; AQ
|
GFFP-SYNGAP1/COL11A2-11604-REAQ |
599nm;467nm |
580nm;418nm |
|
6 |
OR; RE
|
GFFP-SYNGAP1/COL11A2-11604-ORRE |
573nm;599nm |
548nm;580nm |
|
7 |
OR; OR
|
GFFP-SYNGAP1/COL11A2-11604-OROR |
573nm;573nm |
548nm;548nm |
|
8 |
OR; GO
|
GFFP-SYNGAP1/COL11A2-11604-ORGO |
573nm;551nm |
548nm;525nm |
|
9 |
OR; GR
|
GFFP-SYNGAP1/COL11A2-11604-ORGR |
573nm;515nm |
548nm;491nm |
|
10 |
OR; AQ
|
GFFP-SYNGAP1/COL11A2-11604-ORAQ |
573nm;467nm |
548nm;418nm |
|
11 |
GO; RE
|
GFFP-SYNGAP1/COL11A2-11604-GORE |
551nm;599nm |
525nm;580nm |
|
12 |
GO; OR
|
GFFP-SYNGAP1/COL11A2-11604-GOOR |
551nm;573nm |
525nm;548nm |
|
13 |
GO; GO
|
GFFP-SYNGAP1/COL11A2-11604-GOGO |
551nm;551nm |
525nm;525nm |
|
14 |
GO; GR
|
GFFP-SYNGAP1/COL11A2-11604-GOGR |
551nm;515nm |
525nm;491nm |
|
15 |
GO; AQ
|
GFFP-SYNGAP1/COL11A2-11604-GOAQ |
551nm;467nm |
525nm;418nm |
|
16 |
GR; RE
|
GFFP-SYNGAP1/COL11A2-11604-GRRE |
515nm;599nm |
491nm;580nm |
|
17 |
GR; OR
|
GFFP-SYNGAP1/COL11A2-11604-GROR |
515nm;573nm |
491nm;548nm |
|
18 |
GR; GO
|
GFFP-SYNGAP1/COL11A2-11604-GRGO |
515nm;551nm |
491nm;525nm |
|
19 |
GR; GR
|
GFFP-SYNGAP1/COL11A2-11604-GRGR |
515nm;515nm |
491nm;491nm |
|
20 |
GR; AQ
|
GFFP-SYNGAP1/COL11A2-11604-GRAQ |
515nm;467nm |
491nm;418nm |
|
21 |
AQ; RE
|
GFFP-SYNGAP1/COL11A2-11604-AQRE |
467nm;599nm |
418nm;580nm |
|
22 |
AQ; OR
|
GFFP-SYNGAP1/COL11A2-11604-AQOR |
467nm;573nm |
418nm;548nm |
|
23 |
AQ; GO
|
GFFP-SYNGAP1/COL11A2-11604-AQGO |
467nm;551nm |
418nm;525nm |
|
24 |
AQ; GR
|
GFFP-SYNGAP1/COL11A2-11604-AQGR |
467nm;515nm |
418nm;491nm |
|
25 |
AQ; AQ
|
GFFP-SYNGAP1/COL11A2-11604-AQAQ |
467nm;467nm |
418nm;418nm |
|
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