Gene-specific Copy Number Variation Probe-LMAN1
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| Catalog: |
CNVFP-LMAN1-10546 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (LMAN1). 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: |
LMAN1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to LMAN1 genes. This product achieves the purpose of detection by hybridizing with the LMAN1 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 |
Lectin, Mannose Binding 1 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a membrane mannose-specific lectin that cycles between the endoplasmic reticulum, endoplasmic reticulum-Golgi intermediate compartment, and cis-Golgi, functioning as a cargo receptor for glycoprotein transport. The protein has an N-terminal signal sequence, a calcium-dependent and pH-sensitive carbohydrate recognition domain, a stalk region that functions in oligomerization, a transmembrane domain, and a short cytoplasmic domain required for organelle targeting. Allelic variants of this gene are associated with the autosomal recessive disorder combined factor V-factor VIII deficiency. [provided by RefSeq, Jul 2015] |
| Gene Symbol |
LMAN1 |
| Location |
18q21.32 |
| Chromosome |
Chromosome18 |
| Coordinates |
This gene maps to 56995055-57026508 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-LMAN1-10546-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-LMAN1-10546-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-LMAN1-10546-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-LMAN1-10546-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-LMAN1-10546-AQ |
467nm |
418nm |
|
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