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Gene-specific Copy Number Variation Probe-HNRNPA1

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Catalog: CNVFP-HNRNPA1-06708
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HNRNPA1). 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: HNRNPA1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HNRNPA1 genes. This product achieves the purpose of detection by hybridizing with the HNRNPA1 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 Heterogeneous Nuclear Ribonucleoprotein A1
Gene Summary [Provided by RefSeq] This gene encodes a member of a family of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs), which are RNA-binding proteins that associate with pre-mRNAs in the nucleus and influence pre-mRNA processing, as well as other aspects of mRNA metabolism and transport. The protein encoded by this gene is one of the most abundant core proteins of hnRNP complexes and plays a key role in the regulation of alternative splicing. Mutations in this gene have been observed in individuals with amyotrophic lateral sclerosis 20. Multiple alternatively spliced transcript variants have been found. There are numerous pseudogenes of this gene distributed throughout the genome. [provided by RefSeq, Feb 2016]
Gene Symbol HNRNPA1
Location 12q13.13
Chromosome Chromosome12
Coordinates This gene maps to 54674487-54679030 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-HNRNPA1-06708-OR 573nm 548nm
2 RE CNVFP-HNRNPA1-06708-RE 599nm 580nm
3 GO CNVFP-HNRNPA1-06708-GO 551nm 525nm
4 GR CNVFP-HNRNPA1-06708-GR 515nm 491nm
5 AQ CNVFP-HNRNPA1-06708-AQ 467nm 418nm

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